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Organic Produce, Organic Seeds & Organic Products

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add to favorites USP 32 Piroxicam CAS 36322-90-4 for Anti-inflammatory Treatment (jerryzhang001@chembj.com) 211100 Other
USP 32 Piroxicam CAS 36322-90-4 for Anti-inflammatory Treatment

Piroxicam
CAS: 36322-90-4
MF: C15H13N3O4S
MW: 331.35
EINECS: 252-974-3
Chemical Properties:White powder
Assay:99%
Active Pharmaceutical Ingredients; APIs; Piroxicam; All Inhibitors; Inhibitors; Intermediates & Fine Chemicals; Pharmaceuticals; API's; Lipid signaling; Sulfur & Selenium Compounds.
Usage: Antipyretic analgesic active pharmaceutical ingredients.:Non-steroidal anti-inflammatory with long half-life. Cyclooxygenase inhibitor.
Packing:25kg/paper barrel or as required;

Description:
Piroxicam, in some countries. it is spelt piroksikam or piroxikam) is a non-steroidal anti-inflammatory drug (NSAID) of the oxicam class used to relieve the symptoms of painful, inflammatory conditions like arthritis. Piroxicam works by preventing the production of a certain type of body chemical called prostaglandins which are involved in the mediation of pain, stiffness, tenderness and swelling.The medicine is available as capsules, tablets and (not in all countries) as a prescription-free gel 0.5%. It is also available in a betadex formulation, which allows a more rapid absorption of piroxicam from the digestive tract.
Application:
Piroxicam is used to reduce pain, swelling, and joint stiffness from arthritis. Reducing these symptoms helps you do more of your normal daily activities. This medication is known as a nonsteroidal anti-inflammatory drug (NSAID). It works by blocking your body's production of certain natural substances that cause inflammation.
If you are treating a chronic condition such as arthritis, ask your doctor about non-drug treatments and/or using other medications to treat your pain. See also Warning section.
add to favorites Estradiol Benzoate CAS 50-50-0  for development and functioning of the reproductive system (jerryzhang001@chembj.com) 211100 Other
Estradiol Benzoate CAS 50-50-0  for development and functioning of the reproductive system

What is Estradiol Benzoate?

Estradiol Benzoate is a sex hormone that is present in both males and females, and is the most important form of estrogen in humans. In women, it plays a key role in the development and functioning of the reproductive system, as well as in the growth of certain bones. It also governs the distribution of body fat in women and is the main hormone responsible for the fact that women are shorter than men, on average. Both the ovaries and the adrenal glands produce it.

Estradiol Benzoate
Synonyms: (17beta)-Estra-1,3,5(10)-triene-3,17-diol 3-benzoate;1,3,5(10)-Estratriene-3,17-diol-3-benzoate;1,3,5(10)-Oestratriene-3,17-beta-diol 3-benzoate;1,3,5(10)-oestratriene-3,17-beta-diol3-benzoate;17beta-Estradiol monobenzoate;17-beta-estradiolmonobenzoate;17-beta-Oestradiol 3-benzoate;17-beta-oestradiol3-benzoate 
CAS: 50-50-0 
MF: C25H28O3 
MW: 376.49 
EINECS: 200-043-7 
Chemical Properties : White solid 
Usage: Estradiol is the major estrogen secreted by the premenopausal ovary. Estradiol benzoate is an estradiol analog which contains a benzyl ester at the C-3 position. Estradiol benzoate is useful in the treatment of lesions produced by diminution of bodily production of estrogens.

Description
Estradiol benzoate (INN) (brand names Agofollin, Diffolisterol, Progynon-B, many others), or oestradiol benzoate (BAN), is a synthetic ester, specifically the 3-benzoyl ester, of the natural estrogen, estradiol. It was the first form of estrogen to be marketed, patented by Schering-Kahlbaum in 1936 in an oil preparation for injectable use and introduced later that year as Progynon-B. Though it is still in use today, it has been mostly superseded by newer forms of estradiol with improved pharmacokinetics that require less frequent administration such as estradiol cypionate and estradiol valerate.

Medical Uses:
As a sex hormone, Estradiol benzoate triggers many of the developments of the reproductive system that begin in puberty. It is present throughout the reproductive years, and declines during and after menopause. This decline is precisely what causes many of the symptoms of menopause, such as hot flashes and night sweats, vaginal dryness, and the loss of bone mass that may lead to osteoporosis.
A single dose of 2.5 mg estradiol benzoate by intramuscular injection was found to produce plasma estradiol levels of >400 pg/mL, measured 24 hours post-injection, in a group of patients with minimal baseline levels of estradiol (due to GnRH analogue therapy with triptorelin).
add to favorites Tranexamic Acid CAS 1197-18-8 (jerryzhang001@chembj.com) 211100 Other
Tranexamic Acid CAS 1197-18-8

Synonyms: Trans-4-Aminomethylcyclohexane-1-carboxylate; Trans-4-(Aminomethyl)cyclohexanecarboxylic acid; Amstat
CAS: 1197-18-8
EINECS No.: 212-818-4
M. F.: C8H15NO2
M. W.: 157.21
Assay: 99.0-101.0%
Apperance: White crystalline Powder
Type: Anesthetic Agents
Grade Standard: Cosmetic Grade, Medicine Grade
PH: 7.0~8.0
Chloride: 140ppm max
Loss on drying: 0.5%max
Sulfated ash: 0.1%max
Use: Hemostatic effect; (for pharmaceutical and cosmetic use)
Packing: 1kg Aluminum foil bag or 25kg fiber drum;


Description
Tranexamic acid (TXA) is a medication used to treat or prevent excessive blood loss from trauma, surgery, and in various medical conditions including hemophilia and heavy menstrual bleeding. It comes in oral and intravenous forms.
Tranexamic acid is an antifibrinolytic that competitively inhibits the activation of plasminogen to plasmin, a molecule responsible for the degradation of fibrin. Fibrin is the basic framework for the formation of a blood clot in hemostasis.Tranexamic acid has roughly 8 times the antifibrinolytic activity of an older analogue.
Function:
A- For fibrinolytic hemorrhages, such as brain, lung, uterine, the prostate gland, adrenal gland, thyroid gland, trauma or surgical bleeding.
B- Intraoperative early medication or preoperative medication, can reduce bleeding in the operation, and decrease the amount of blood transfusion.
C- Also used in pulmonary hemorrhage, liver cirrhosis hemorrhage and upper gastrointestinal hemorrhage.
D- Used in bleeding caused by fibrinolysis process hyperfunction:
Such as abnormal bleeding of operation for the lung, liver, pancreas, prostate, thyroid, adrenal surgery.
Such as obstetrics and postpartum hemorrhage and tuberculosis hemoptysis or blood-stained sputum, hematuria, prostatic hypertrophy bleeding, upper gastrointestinal bleeding, etc.
E- Can also be used for bleeding caused by excessive streptokinase or urokinase.

Medical Uses
1.Hemostatic, significant effect on traumatic bleeding, preoperative prophylactic medication can decrease operation hemorrhage.
2. The chemical structure of tranexamic acid and lysine, competitive inhibition of plasminogen to fibrin adsorption, to prevent their activation, protect the fiber protein was not degraded by the enzyme and dissolved, ultimately achieve hemostasis effect.
3. All applicable in the treatment of acute or chronic, localized or systemic primary fibrinolysis hyperfunction caused by bleeding, such as obstetric hemorrhage, renal hemorrhage, hypertrophy of the prostate, hemophilia hemorrhage, pulmonary tuberculosis hemoptysis, bleeding in the stomach, liver, lung, spleen and other organs of hemorrhage after operation
4. The clinical effect of tranexamic acid on insect bites, eczema and dermatitis, simple purpura, chronic urticaria, artificial sex urticaria, rash and drug poisoning effect, also have certain effects on erythroderma, scleroderma, SLE, erythema multiforme, herpes zoster and alopecia areata, curative effect of hereditary angioedema is also good.
add to favorites Acitretin CAS 55079-83-9 (jerryzhang001@chembj.com) 211100 Other
Acitretin CAS 55079-83-9

Chemical information
Product name:Acitretin
CAS No.:55079-83-9
Molecular formula:C21H26O3
Molecular weight:326.43
Product Specifications:Pharmacopoeial grade;

Description
Acitretin (trade names Soriatane and Neotigason) is a second-generation retinoid. It is taken orally, and is typically used for psoriasis.
It is a metabolite of etretinate, which was used prior to the introduction of acitretin. Etretinate was discontinued because it had a narrow therapeutic index as well as a long elimination half-life (t1/2=120 days), making dosing difficult. In contrast, acitretin's half-life is approximately 2 days. However, because acitretin can be reverse metabolised into etretinate which has an extremely long half-life, women must avoid becoming pregnant for at least 3 years after discontinuing acitretin. Therefore, acitretin is generally not recommended for women of child-bearing age with a risk of becoming pregnant.

Medical Uses:
Acitretin is an oral retinoid used in the treatment of severe resistant psoriasis. Because of the potential for problems and severe side effects it is generally used in only very severe cases of psoriasis that have been unresponsive to other treatments. It binds to nuclear receptors that regulates gene transcription. They induce keratinocyte differentiation and reduce epidermal hyperplasia, leading to the slowing of cell reproduction. Acitretin is readily absorbed and widely distributed after oral administration. A therapeutic effect occurs after 2 to 4 weeks or longer.
Patients that have received the medication are advised against giving blood for at least 3 years due to the risk of birth defects.

Adverse effect:
Acitretin is noted for the possibility of severe birth defects and should not be used by pregnant women or women planning to get pregnant within 3 years following the use of acitretin. Sexually active women of childbearing age who use acitretin should also use at least 2 forms of birth control concurrently. Men and women who use it should not donate blood for 3 years after using it, because of the possibility that the blood might be used in a pregnant patient and cause birth defects. In addition, it may cause nausea, headache, itching, dry, red or flaky skin, dry or red eyes, dry or chapped lips, swollen lips, dry mouth, thirst, cystitis acne or hair loss.
add to favorites Anxiolytic Injectable Hormones Selank Polypeptide 5mg/vial reliever of anxiety (jerryzhang001@chembj.com) 211100 Other
Anxiolytic Injectable Hormones Selank Polypeptide 5mg/vial reliever of anxiety


Selank
Alias: Selanc
Sequence: Thr-Lys-Pro-Arg-Pro-Gly-Pro
MF: C33H57N11O9
MW: 751.9
Purity: 99%
Specification: 5mg/vial
Appearance: White Powder
Place of Origin: China
Standard: USP
Certification: SGS
Method of Analysis: HPLC
Packaging Details: Very discreet. As required.

2. What is Selank ?
Selank  is a nootropic, anxiolytic peptide based drug developed by the Institute of Molecular Genetics of the Russian Academy of Sciences. Selank is a heptapeptide with the sequence Thr-Lys-Pro-Arg-Pro-Gly-Pro. It is a synthetic analogue of a human tetrapeptide tuftsin.
Neuropeptide Selank is a synthetic derivative of the human body's naturally produced tetrapeptide Tuftsin. Selank is used as an anxiolytic in the therapy of anxiety and phobic disorders, including generalized anxiety. Its action is similar to that of mild benzodiazepins but without the sedative effects. As a selective anxiolytic with a nootropic component, Selank can be used as treatment of depression, fear and general anxiety. It also reduces phsychic tension.

Medical Application:
Selank is classified as a nootropic-anxiolytic type drug, it uses extend beyond the relief of anxiety and improved cognitive functioning alone. A few areas in which Selank may find itself useful are: Stress reduction, the alleviation of depression, reversal of anhedonia, improvement in mood in emotionally stable individuals, and cessation of insomnia. Of course, with Selank being a nootropic-anxiolytic, it also prove useful for the treatment of different forms of anxiety, such as G. A. D (generalized anxiety disorder), S. A. D (social anxiety disorder), Panic Disorder, as well as non-diagnosed bouts of anxiety. As a nootropic, Selank can help enhance mental sharpness, reduce mental fatigue, improve the ability to focus, improve cognitive functioning while in a sleep deficit, and enhance memory.
add to favorites Anxiolytic Injectable Hormones Selank Polypeptide 5mg/vial reliever of anxiety (jerryzhang001@chembj.com) 211100 Other
Anxiolytic Injectable Hormones Selank Polypeptide 5mg/vial reliever of anxiety


Selank
Alias: Selanc
Sequence: Thr-Lys-Pro-Arg-Pro-Gly-Pro
MF: C33H57N11O9
MW: 751.9
Purity: 99%
Specification: 5mg/vial
Appearance: White Powder
Place of Origin: China
Standard: USP
Certification: SGS
Method of Analysis: HPLC
Packaging Details: Very discreet. As required.

2. What is Selank ?
Selank  is a nootropic, anxiolytic peptide based drug developed by the Institute of Molecular Genetics of the Russian Academy of Sciences. Selank is a heptapeptide with the sequence Thr-Lys-Pro-Arg-Pro-Gly-Pro. It is a synthetic analogue of a human tetrapeptide tuftsin.
Neuropeptide Selank is a synthetic derivative of the human body's naturally produced tetrapeptide Tuftsin. Selank is used as an anxiolytic in the therapy of anxiety and phobic disorders, including generalized anxiety. Its action is similar to that of mild benzodiazepins but without the sedative effects. As a selective anxiolytic with a nootropic component, Selank can be used as treatment of depression, fear and general anxiety. It also reduces phsychic tension.

Medical Application:
Selank is classified as a nootropic-anxiolytic type drug, it uses extend beyond the relief of anxiety and improved cognitive functioning alone. A few areas in which Selank may find itself useful are: Stress reduction, the alleviation of depression, reversal of anhedonia, improvement in mood in emotionally stable individuals, and cessation of insomnia. Of course, with Selank being a nootropic-anxiolytic, it also prove useful for the treatment of different forms of anxiety, such as G. A. D (generalized anxiety disorder), S. A. D (social anxiety disorder), Panic Disorder, as well as non-diagnosed bouts of anxiety. As a nootropic, Selank can help enhance mental sharpness, reduce mental fatigue, improve the ability to focus, improve cognitive functioning while in a sleep deficit, and enhance memory.

Selank effects:
Experimental and clinical studies showed the following pharmaclogical effects of Selank:
improvement of learning and memory processes (reference, reference)
increased sensory attention
increased curiosity
increased mental clarity
restoration of balance of serotonergic and noradrenergic brain system activity (reference)
anti-anxiety - inhibition of anxiety (reference)
antiviral activity with no negative effects (reference)
psychostimulant, anti-asthenic - increased mental energy (reference)
stabilization of mood and overall feeling of wellbeing
reversal of anhedonia (restoring the feeling of pleasure)
potential restoration of catecholaminergic system functions after damage due to drug abuse reference
add to favorites Ropivacaine hydrochloride CAS 132112-35-7  (jerryzhang001@chembj.com) 211100 Other
Ropivacaine hydrochloride CAS 132112-35-7 
 
Synonyms: S-ROPIVACAINE HCL;(S)-ROPIVACAINE HYDROCHLORIDE;ROPIVACAINE HYDROCHLORIDE MONOHYDRATE;ROPIVCACAINE HYDROCHLORIDE;ROPIVACAINE HCL;(S)-1-propyl-2',6'-dimethylanilinoformoxylpiperidine monohydrochloride monohydrate;(S)-1-propyl-2',6'-dimethylanilinoformoxylpiperidine,monohydrochloride,monohydrate;(S)-Ropivaxaine hydrochloride 
CAS: 132112-35-7 
MF: C17H26N2O.ClH.H2O 
MW: 328.88 
 
Chemical Properties : White Solid;

Description
Ropivacaine is a local anaesthetic drug belonging to the amino amide group. The name ropivacaine refers to both the racemate and the marketed S-enantiomer. Ropivacaine hydrochloride is commonly marketed by AstraZeneca under the trade name Naropin.

Medical Uses:
Ropivacaine is indicated for local anaesthesia including infiltration, nerve block, epidural and intrathecal anaesthesia in adults and children over 12 years. It is also indicated for peripheral nerve block and caudal epidural in children 1–12 years for surgical pain. It is also sometimes used for infiltration anaesthesia for surgical pain in children.
Ropivacaine is often coadministered with fentanyl for epidural analgesia, for example in pregnant women during labour.
add to favorites Promethazine hydrochloride CAS 58-33-3 (jerryzhang001@chembj.com) 211100 Other
Promethazine hydrochloride CAS 58-33-3


Promethazine HCl
Product Name: Promethazine hydrochloride
Promethazine HCl CAS: 58-33-3
Promethazine HCl MF: C17H21ClN2S
Promethazine HCl MW: 320.88
Promethazine HCl EINECS: 200-375-2
Promethazine HCl MP: 230-232 °C
Promethazine HCl Storage: Temp. Refrigerator
Promethazine HCl Merck: 13, 7878
Promethazine HCl Apperance: White Solid
Promethazine HCl Usage: Antihistaminic, antiemetic, CNS depressant; Stool softener

Specification:
Product name: Promethazine hydrochloride
Other Name 10-(2-dimethylamino-1-propyl)phenothiazine hydrochloride;PROMETHAZINE HCL;PROMETHAZINE HYDROCHLORIDE;PHENERGAN;10-(2-(dimethylamino)propyl)phenothiazinemonohydrochloride;10-(2-(dimethylamino)propyl)-phenothiazinmonohydrochloride;10-(2-dimethylaminopropyl)phenothiazinehydrochloride;10-(3-dimethylaminoisopropyl)phenothiazinehydrochloride
Original China
CAS 58-33-3
Molecular formula C17H21ClN2S
EINECS 200-375-2
Molecular Weight 320.88
Brand name NJBNSteroid
Delivery time within 24 hours upon receipt of payment
Delivery Fast and secure shipping by EMS, DHL, TNT, FedEx, UPS
Purity 99%
Package Discreet and Hidden package according to specific requirement
Appearance White powder
Certification SGS, ISO 9001, KOSHER
Payment Terms Western Union, Money Gram , T/T, Bitcoin
Minimum Order Quantity 10g
Price Negotiable
Usage Antihistaminic, antiemetic, CNS depressant; Stool softener
MF





Description

Promethazine is a neuroleptic medication and first-generation antihistamine of the phenothiazine family. The drug has strong sedative and weak antipsychotic effects. It also reduces motion sickness and has antiemetic and anticholinergic properties (via its action on the dopamine receptor D2). In some countries it is prescribed for insomnia when benzodiazepines are contraindicated. It is available in many countries under many brand names. Promethazine was developed in the mid 1940s when a team of scientists from Rhône-Poulenc laboratories were able to synthesize it from phenothiazine and a diamine side chain of diphenhydramine

Promethazine hydrochloride occurs as a white to faint yellow, practically odorless, crystalline powder which slowly oxidizes and turns blue on prolonged exposure to air. It is soluble in water and freely soluble in alcohol.
Each tablet, for oral administration, contains 25 mg or 50 mg of promethazine hydrochloride. In addition each tablet contains the following inactive ingredients: dibasic calcium phosphate, magnesium stearate, microcrystalline cellulose, sodium starch glycolate and stearic acid.
Promethazine Hydrochloride Tablets USP, 50 mg also contain anhydrous lactose.

Medical Uses:

Promethazine is used to prevent and treat nausea and vomiting related to certain conditions (such as before/after surgery, motion sickness). It is also used to treat allergy symptoms such as rash, itching, and runny nose. It may be used to help you feel sleepy/relaxed before and after surgery or to help certain narcotic pain relievers (such as meperidine) work better. It may also be used for a short time to treat a runny nose due to the common cold.

Promethazine is an antihistamine and works by blocking a certain natural substance (histamine) that your body makes during an allergic reaction. Its other effects (such as anti-nausea, calming, pain relief) may work by affecting other natural substances (such as acetylcholine) and by acting directly on certain parts of the brain.


Perennial and seasonal allergic rhinitis.
add to favorites Pramoxine Hydrochloride CAS 637-58-1 (jerryzhang001@chembj.com) 211100 Other
Pramoxine Hydrochloride CAS 637-58-1
CAS: 637-58-1
EINECS number: 211-293-1
Molecular formula: C17H28ClNO3
Molecular Weight: 329.8621
Boiling point: 427 ° C at 760 mmHg
Flash Point: 123.5 ° C
Vapor Pressure: 1.7E-07mmHg at 25 ° C
Appearance: White or almost white crystalline powder
Uses:Surgical anesthesia:Epidural anesthesia (including epidural anesthesia during cesarean section);Local infiltration anesthesia. 
Acute pain control:For postoperative or labor analgesia continuous epidural infusion can be used can also be intermittent medication;Local infiltration anesthesia.



1. Description

Pramocaine (INN and BAN, also known as pramoxine or pramoxine HCI) is a topical anesthetic discovered at Abbott Laboratories in 1953 and used as an antipruritic. Chemically, it is p-n butoxyphenyl gammamorpholinopropyl ether hydrochloride.
 Pharmacologic study revealed it to be potent and of low acute and subacute toxicity, well tolerated by most mucous membranes and of a low sensitizing index in humans.Like other local anesthetics, paramoxine decreases the permeability of neuronal membranes to sodium ions, blocking both initiation and conduction of nerve impulses. Depolarization and repolarization of excitable neural membranes is thus inhibited, leading to numbness.
The popular itch creams Gold Bond and some forms of Calamine Lotion use pramocaine hydrochloride to numb sensitive skin, as does the pain relief variant of Neosporin and some formulations of Sarna. The hydrochloride salt form of pramocaine is water-soluble.
Medical Application:
Pramoxine belongs to a class of drugs known as local anesthetics. It works by numbing the skin to block the feelings of pain and itching.
Pramoxine is used to temporarily relieve itching and pain caused by minor skin irritation such as minor burns/cuts/scrapes, sunburn, eczema, insect bites, cold sores, or rashes from poison ivy, poison oak, or poison sumac. Some products containing pramoxine are also used to temporarily relieve the itching and discomfort from hemorrhoids and certain other problems of the genital/anal area (such as anal fissures, itching around the vagina/rectum).
add to favorites Tetracaine hydrochloride CAS 136-47-0 (jerryzhang001@chembj.com) 211100 Other
Tetracaine hydrochloride CAS 136-47-0

Tetracaine hydrochloride
English Synonyms:
L AND OCAIN HYDROCHLORIDE;INTERCAIN HYDROCHLORIDE;MEETHOBALM HYDROCHLORIDE;2-(DIMETHYLAMINO)ETHYL 4-(N-BUTYLAMINO)BENZOATE HYDROCHLORIDE;2-DIMETHYLAMINOETHYL ESTER OFP-BUTYLAMINOBENZOIC ACID HYDROCHLORIDE;4-(N-BUTYLAMINO)BENZOIC ACID 2-(DIMETHYLAMINO)ETHYL ESTER HYDROCHLORIDE;4-[BUTYLAMINO]BENZOIC ACID-2-[DIMETHYLAMINO]ETHYL ESTER HYDROCHLORIDE;4-BUTYLAMINOBENZOIC ACID DIMETHYLAMINOETHYL ESTER HCL
CAS NO.: 136-47-0
EINECS: 205-248-5
Assay: 98%
Molecular Formula: C15H25ClN2O2
Molecular Weight: 300.82
Quality Standard: USP31
Packing: foil bag/tin
Usage: A local anesthetic used topically in opthalmology.

2. What is Tetracaine HCl?
Tetracaine (also known as amethocaine) is a local anesthetic of the ester anesthetic group. It is mainly used topically in ophthalmology and as an antipruritic, and it has been used in spinal anesthesia.
In biomedical research, tetracaine is used to alter the function of calcium release channels (ryanodine receptors) that control the release of calcium from intracellular stores. Tetracaine is an allosteric blocker of channel function. At low concentrations, tetracaine causes an initial inhibition of spontaneous calcium release events, while at high concentrations, tetracaine blocks release completely.
Tetracaine is the T in TAC, a mixture of 5 to 12 per cent tetracaine, 0.05 per cent adrenaline, and 4 or 10 percent cocaine hydrochloride used in ear, nose & throat surgery and in the emergency department where numbing of the surface is needed rapidly, especially when children have been injured in the eye, ear, or other sensitive locations.
It is on the World Health Organization's List of Essential Medicines, a list of the most important medication needed in a basic health system.

Medical Uses:

It is taken as Spinal anesthesia (high, low, saddle block) and topically to produce surface anesthesia:
Eye: To anesthetize conjunctiva and cornea prior to superficial procedures (including tonometry, gonioscopy, removal of foreign bodies or sutures, corneal scraping).
Nose and Throat: To abolish laryngeal and esophageal reflexes prior to bronchoscopy, esophagoscopy. 
Skin: To relieve pruritus, pain, burning.
add to favorites Estradiol valerate CAS 979-32-8 as female hormone (jerryzhang001@chembj.com) 211100 Other
Estradiol valerate CAS 979-32-8 as female hormone

English Name: Estradiol valerate
Other Name: Oestradiol Valerate; estradiol-17-valerate
CAS: 979-32-8
EINECS Number: 213-559-2
Formula: C23H32O3
MW: 356.4984
Assay:99.8%
Appearance: White Crystalline powder
Uses: For the treatment of amenorrhea, menopausal symptoms, reduce milk secretion, prostate cancer;

2. Description
Estradiol valerate (EV, E2V) (INN, USAN, JAN) (brand names Altadiol,Deladiol, Delestrogen, Estraval, Lastrogen, Progynova, Valergen, many others), or oestradiol valerate (BAN), is a synthetic ester, specifically the 17-pentanoyl ester, of the natural estrogen, 17beta-estradiol. It was first introduced, as Delestrogen by Squibb in the United States, in 1954, and along with estradiol benzoate (1936) and estradiol cypionate (1952),has since become one of the most widely used esters of estradiol.

Medical Uses:
This medication is a female hormone (estrogen). It is used by women to help reduce symptoms of menopause (such as hot flashes, vaginal dryness). These symptoms are caused by the body making less estrogen. If you are using this medication to treat symptoms only in and around the vagina, products applied directly inside the vagina should be considered before medications that are taken by mouth, absorbed through the skin, or injected. This medication may also be used by women who are not able to produce enough estrogen (for example, due to hypogonadism, primary ovarian failure) and by men to treat prostate cancer.
Estradiol valerate is a female estrogen hormone. It works by replacing natural estrogens in a woman who can no longer produce enough estrogen.It works for advanced prostate cancer by antagonizing male hormones.
add to favorites Riboflavin CAS 83-88-5 as food additive (jerryzhang001@chembj.com) 211100 Other
Riboflavin CAS 83-88-5 as food additive

Name: Riboflavin, Vitamin B2
Other name: Lactoflavine; Vitamin B2 (Riboflavine); Riboflavin Vitamin B2; E 101; Riboflavin (1.07609); Riboflavine; Vitamin B2 Feed Grade; Vitamin B_2; Vitamin B2; Riboflavin (VB2); 1-deoxy-1-(7,8-dimethyl-2,4-dioxo-3,4-dihydrobenzo[g]pteridin-10(2H)-yl)pentitol; 5-deoxy-5-(7,8-dimethyl-2,4-dioxo-3,4-dihydrobenzo[g]pteridin-10(2H)-yl)-D-ribitol; 1-deoxy-1-(7,8-dimethyl-2,4-dioxo-3,4-dihydrobenzo[g]pteridin-10(2H)-yl)-D-ribitol; VITAMIN G; Riboflavin(VB2)
CAS No.: 83-88-5
EINECS No.: 201-507-1
M.F. : C17H20N4O6
M.W. : 376.3639
Appearance: Orange yellow crystalline powder;

2. What is Riboflavin (vitamin B2) ?
Riboflavin (vitamin B2) is part of the vitamin B group. It is the central component of the cofactors FAD and FMN and as such required for a variety of flavoprotein enzyme reactions including activation of other vitamins. It was formerly known as vitamin G.
As a chemical compound, riboflavin is a yellow-orange solid substance with poor solubility in water compared to other B vitamins. Visually, it imparts color to vitamin supplements (and bright yellow color to the urine of persons taking a lot of it).

Medical Uses:
Riboflavin has been used in several clinical and therapeutic situations. For over 30 years, riboflavin supplements have been used as part of the phototherapy treatment of neonatal jaundice. The light used to irradiate the infants breaks down not only bilirubin, the toxin causing the jaundice, but also the naturally occurring riboflavin within the infant's blood, so extra supplementation is necessary.

It is Used for recovery after illness and various diseases caused by lack of riboflavin. It is also used for prevention and control of the inflammation in mouth, eyes and externalia: Such as deficiency, cheilitis, glossitis, conjunctivitis and scrotitis, etc.

One clinical trial found that high-dose riboflavin appears to be useful alone or along with beta-blockers in the prevention of migraine. A dose of 400 mg daily has been used effectively in the prophylaxis of migraines, especially in combination with a daily supplement of magnesium citrate 500 mg.

Industrial Use:
Because riboflavin is fluorescent under UV light, dilute solutions (0.015-0.025% w/w) are often used to detect leaks or to demonstrate coverage in an industrial system such a chemical blend tank or bioreactor. (See the ASME BPE section on Testing and Inspection for additional details.)
 
add to favorites  Triamcinolone Acetonide CAS 76-25-5 Anti-inflammatory hormone (jerryzhang001@chembj.com) 211100 Other
 Triamcinolone Acetonide CAS 76-25-5 Anti-inflammatory hormone

Triamcinolone Acetonide
CAS: 76-25-5
MF: C24H31FO6
MW: 434.5
EINECS: 200-948-7
Type: Anti-inflammatory hormone 
Grade Standard:  Medicine Grade 
Apperance:  white or off-white powder 
Density: 1.33g/cm3 
Melting point::274-278℃ (dec.) Lead time:  1-3days Sample:  Available 
Packaging Details: 30mg/foil bag , or 50mg/bottle as your request 
Delivery Detail: within 2 days 
Appearance :white crystal  powder 
Storage:Store in a cool, dry place and keep away from direct strong light. hydrocortisone butyrate
Function: Anti-inflammatory hormone;


Description:
Triamcinolone acetonide is a kind of long-term glucocorticoid drugs.  It belongs to adrenocorticotropic hormone drugs. It is the derivative of Triamcinolone, and with the same function as Triamcinolone.
Triamcinolone acetonide, its acetate form appears to be white or white-like crystalline powder. The drug is odorless, with bitter taste. It is hardly soluble in water, slightly soluble in ethanol, soluble in chloroform, and slightly soluble in acetone.
Medical Function:
Clinically triamcinolone acetonide is used for treatment of various skin diseases such as atopic dermatitis, contact dermatitis, seborrheic dermatitis, neurodermatitis, eczema, psoriasis, psoriasis, lichen planus and skin pruritus, as well as bronchial asthma, rheumatoid arthritis, acute sprains, chronic ache in back and legs, frozen shoulder, tenosynovitis, ophthalmic inflammation, oral mucosal congestion, erosion, ulcers, granulomatous cheilitis, and oral mucosa chronic infectious diseases.
Furthermore, it can also be used for local injection treatment in keloid, cystic acne, discoid lupus erythematosus, alopecia areata and other small area of damages. Triamcinolone acetonide nasal spray can be used for the prevention and treatment of perennial, seasonal allergic rhinitis, and vasomotor rhinitis. Intra-articular injection of this drug can eliminate inflammation and pain, swelling or can alleviate, pain, stiffness and swelling feeling.
How it functions
Taking orally 5mg of the drug yields a bioavailability of about 23%. Its plasma concentration reaches peak (105 ng/mL) within one hour with the half-life is being 2 hours; It has a slow intramuscular absorption rate which takes effect within hours, and gives maximal effect within 1 to 2 days. The effect can be maintained for 2 ~ 3 weeks; the absorption rate of intradermal and intra-articular injection of the drug is low, but has a long-lasting effect; generally the efficacy can be maintained for more than 1-2 week per injection. This product has a low binding rate with plasma albumin protein, and is metabolized into non-active product in the liver, kidneys and tissues which is then further excreted by the kidneys. 
add to favorites Procaine CAS 59-46-1 for for local anesthesia (jerryzhang001@chembj.com) 211100 Other
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Procaine CAS 59-46-1 for for local anesthesia

Procaine
CAS: 59-46-1
MF: C13H20N2O2
MW: 236.31
EINECS: 200-426-9
Usage: Procaine is a kind of local anesthetics. With low toxicity but quick and safe effects, procaine is suitable for local anesthesia, applied to the eye, ear, nose, teeth and other department operation, used for infiltration anesthesia, anesthesia and closed therapy supervisor. Procaine is also used in the production of procaine penicillin.

Description

Procaine is a local anesthetic drug of the amino ester group. It is used primarily to reduce the pain of intramuscular injection of penicillin, and it is also used in dentistry. Owing to the ubiquity of the trade name Novocain, in some regions procaine is referred to generically as novocaine.
It acts mainly as a sodium channel blocker. Today it is used therapeutically in some countries due to its sympatholytic, anti-inflammatory, perfusion enhancing, and mood enhancing effects.

Medical Application:
Procaine is a kind of local anesthetics. With low toxicity but quick and safe effects, procaine is suitable for local anesthesia, applied to the eye, ear, nose, teeth and other department operation, used for infiltration anesthesia, anesthesia and closed therapy supervisor. Procaine is also used in the production of procaine penicillin.
A 1% procaine injection has been recommended for the treatment of extravasation complications associated with venipuncture (along with moist heat, ASA, steroids, antibiotics). It has likewise been recommended for treatment of inadvertent intra-arterial injections (10 ml of 1% procaine), as it helps relieve pain and vascular spasm.
Procaine is used as an injection during surgery and other medical and dental procedures.
add to favorites  Imiquimod CAS  99011-02-6 for Treatment of adult genital and perianal warts (jerryzhang001@chembj.com) 211100 Other
 Imiquimod CAS  99011-02-6 for Treatment of adult genital and perianal warts

Product Name:    Imiquimod
Synonyms:    R-837;S-26308;1-(2-METHYLPROPYL)-1H-IMIDAZO[4,5-C]QUINOLIN-4-AMINE;4-amino-1-isobutyl-1h-imidazo[4,5-c]quinoline;ALDARA;IMIQUIMOD;1-isoButyl-1H-Inudazole[4.5-c]quinoline-4-amine;1-(2-Methylpropyl)-1H-imidazo[4,5-c]quinolin-4-amine, R-837, S-26308, Aldara
CAS:    99011-02-6
MF:    C14H16N4
MW:    240.3
Mol File:    99011-02-6.mol ;

Description:
Imiquimod is a kind of imidozoquinoline amine-class interleukin agonist developed by the 3M Pharmaceuticals Company (US), belonging to the drug for the treatment of genital warts. Upon being applied to the mice skin, it can induce the cytokinesis and produce 伪-interferon, tumor necrosis factor and many kinds of interleukins.
Imiquimod itself has no direct effect on the virus itself, but instead through stimulating the body for producing cytokines and stimulating immune response to eliminate the wart tissue and reduce the viral erosion. 

Medical Function:
Clinically, Imiquimod can be used as the immunomodulators in the treatment of adult genital and perianal warts with convenient application, well tolerance and unique mechanism of action which makes it be the first-choice drug for treatment of genital warts. In addition, there are reports that imiquimod can be used for treating viral skin diseases including common warts, flat warts, molluscum and herpes simplex virus.
It can also be effective in treating basal cell carcinoma, Bowen's disease, Bowen papulosis, actinic keratosis, and skin tumors such as cutaneous T-cell tumor and Kaposi's sarcoma. It may also be effective in treating vitiligo and alopecia areata. 

Usage and Dosage
It can be used for the treatment of adult external genital and perianal genital warts at 3 times per week. Just before sleep, first apply the product evenly in a thin layer on the surface of the wart and gently massage until the product is completely absorbed.
The position of the medication should not be packeted and should be maintained for 6 to 10 hours, and then wash with a neutral soap and clean water for clearing the drugs in the administration site. Wash your hands before and after treatment. 250 mg of cream can be applied to 20cm2 of wart. Avoid excessive application of the drug. Patients should continue the treatment until the wart is completely cleared.
Wart can be cleared within 2-4 week at the fastest speed and can be generally cleared within 8 to 12 weeks. The medication should be not more than 16 weeks. After the treatment, patients with mild erythema locally who does not have to be discontinued for drug; if the patients feel general malaise or get local skin reactions (edema, erosion, pain, etc.), the drug should be discontinued. Only when the reaction is alleviated can they continue the medication.
add to favorites Cloxacillin sodium CAS 7081-44-9 for the treatment of a number of bacterial infections (jerryzhang001@chembj.com) 211100 Other
Cloxacillin sodium CAS 7081-44-9 for the treatment of a number of bacterial infections
 
Product Name: Cloxacillin sodium
Synonyms:bactopen;brl-1621sodiumsaltmonohydrate;cloxacillinsodiummonohydrate;orbeninsodiumhydrate;prostaphlin-amonohydrate;sodiumcloxacillinmonohydrate;staphobristol-250;thyl-4-isoxazolecarboxamido)-3,3-dimethyl-7-oxo-,sodiumsalt,monohydrate
CAS:7081-44-9
MF:C19H19ClN3NaO6S
MW:475.88
EINECS:211-390-9;

1. What is Cloxacillin ?
Cloxacillin is an antibiotic useful for the treatment of a number of bacterial infections. It is semisynthetic and in the same class as penicillin.
Cloxacillin sodium is an antibiotic medication commonly used to treat infections with Staphylococcus bacteria. It has a low risk of side effects, except for a potentially serious allergic reaction in a small number of patients. Before someone starts using cloxacillin sodium, it is advisable to discuss medical history with a medical professional to determine if there are any obvious risk factors for a bad reaction. Another drug may need to be considered to treat the infection.
This medication is in the penicillin family, and is produced through semi-synthetic means. It works by attacking the process bacteria use to synthesize their cell walls, killing them and effectively stopping the infection. The dosage is given orally and may vary depending on the specifics of the infection and the patient’s weight. An adjustment for a patient with kidney impairment may also be necessary, as these patients can’t clear this medication as quickly and require a lower dose.
Usage:
Cloxacillin is used against staphylococci that produce beta-lactamase, due to its large R chain, which does not allow the beta-lactamases to bind. This drug has a weaker antibacterial activity than benzylpenicillin, and is devoid of serious toxicity except for allergic reactions.
Cloxacillin was discovered and developed by Beecham.It is sold under a number of trade names, including Cloxapen, Cloxacap, Tegopen and Orbenin. It is on the World Health Organization's List of Essential Medicines, the most important medication needed in a basic health system.
Cloxacillin is used to treat a wide variety of bacterial infections. This medication is a type of penicillin antibiotic. It works by stopping the growth of bacteria.
This antibiotic treats only bacterial infections. It will not work for viral infections (e.g.,common cold, flu). Unnecessary use or overuse of any antibiotic can lead to its decreased effectiveness.
add to favorites Clobetasol Propionate CAS 25122-46-7 for treatment of the inflammatory and pruritic manifestations (jerryzhang001@chembj.com) 211100 Other
Clobetasol Propionate CAS 25122-46-7 for treatment of the inflammatory and pruritic manifestations

Product Name: Clobetasol Propionate
Synonyms:17-propionate;cgp9555;clobesol;pregna-1,4-diene-3,20-dione,21-chloro-9-fluoro-11-beta,17-dihydroxy-16-beta-me;CLOBESTASOL PROPIONATE;CLOBETASOL-17-PROPIONATE;CLOBETASOLE PROPIONATE;CLOBETASOL PROPIONATE
CAS No.: 25122-46-7
EINECS: 246-634-3
Molecular Formula: C25H32ClFO5
Formula Weight: 466.97
Appearance: White Crystalline Powder
Assay: 99.65%
Packaging and storage:  Preserve in well-closed containers, and store at controlled room temperature.
Usage: For short-term topical treatment of the inflammatory and pruritic manifestations of moderate to severe corticosteroid-responsive dermatoses of the scalp.


2. Description:
Clobetasol propionate  is a corticosteroid of the glucocorticoid class used to treat various skin disorders including eczema and psoriasis. It is also highly effective for contact dermatitis caused by exposure to poison ivy/oak. Clobetasol belongs to US Class I (Europe: class IV) of the corticosteroids, making it one of the most potent available. It comes in shampoo, mousse, ointment and emollient cream presentations. It has very high potency and typically should not be used with occlusive dressings, or for extended continuous use (beyond two weeks). It is also used to treat several autoimmune diseases including alopecia areata, vitiligo, lichen sclerosus, and lichen planus.

Clobetasol propionate is a corticosteroid of the glucocorticoid class used to treat various skin disorders including eczema and psoriasis. It is also highly effective for contact dermatitis caused by exposure to poison ivy/oak. Clobetasol belongs to US Class I (Europe: class IV) of the corticosteroids, making it one of the most potent available.
 
It comes in shampoo, mousse, ointment and emollient cream presentations. It has very high potency and typically should not be used with occlusive dressings, or for extended continuous use (beyond two weeks). It is also used to treat several auto-immune diseases including alopecia areata, vitiligo and lichen planus (auto immune skin nodules).
 
Clobetasol propionate for synthetic efficient local external use sugar cortical hormone drugs. With strong anti-inflammatory, resistance to itch and capillary shrinkage effect, its anti-inflammatory effects of about 112.5 times of hydrocortisone sodium, betamethasone dipropionate ramification 2.3 times, fluocinolone 18.7 times. At the same time a suppression of mitosis Use, can effectively penetrate into skin cutin layer.

As a type of steroid that is applied to the skin, clobetasol topical is used to help relieve redness, itching, swelling, or other discomfort caused by skin conditions. The solution are used for scalp problems, the foam is used for mild to moderate plaque psoriasis, the cream, lotion, and spray are used for moderate to severe plaque psoriasis, and the foam and shampoo are used for moderate to severe scalp psoriasis.

Application:
This medicine is a corticosteroid (cortisone-like medicine or steroid). belongs to a group of medications known as topical steroids and is used to treat inflammation and itching due to a wide variety of skin conditions, such as eczema, psoriasis, dermatitis, and allergic reactions.
 
Clobetasol propionate is a synthetic corticosteroid, for topical dermatologic use. Clobetasol, an analog of prednisolone, has a high degree of glucocorticoid activity and a slight degree of mineralocorticoid activity.

Medical Uses
Clobetasol propionate is used for the treatment of various skin disorders including eczema, herpes labialis,psoriasis, and lichen sclerosus. It is also used to treat several auto-immune diseases including alopecia areata, vitiligo, lichen planus (auto immune skin nodules), and mycosis fungoides (T-cell skin lymphoma). It is used as first-line treatment for both acute and chronic GVHD of the skin.
add to favorites Mometasone Furoate CAS 83919-23-7 for anti-inflammatory (jerryzhang001@chembj.com) 211100 Other
Mometasone Furoate CAS 83919-23-7 for anti-inflammatory

Mometasone Furoate
CAS: 83919-23-7
MF: C27H30Cl2O6
MW: 521.43
Purity: 99%
Package: 1kg/aluminum cans
Appearance: White powder.
USES: Use of corticosteroids in local effect, have anti-inflammatory, relieving itching and vascular contraction effect. For patients with skin diseases, can alleviate inflammation and itching, especially with the reaction of the patients have cortisone.

Description
Mometasone furoate is a glucocorticosteroid used topically to reduce inflammation of the skin or in the airways. It is a prodrug of the free form mometasone.
Mometasone furoate is a synthetic (man-made) steroid hormone in the glucocorticoid family of steroid hormones that is used for the treatment of nasal allergy. The naturally occurring glucocorticoid hormone is cortisol or hydrocortisone which is produced in the adrenal glands. Glucocorticoid hormones are potent reducers of inflammation (anti-inflammatory). When used as a nasal inhaler or spray, medications travel directly to the inner lining of the nose, and very little is absorbed into the body to cause side effects. The FDA approved mometasone in October 1997.

Medical Uses:
Mometasone furoate is used in the treatment of inflammatory skin disorders (such as eczema and psoriasis) (topical form), allergic rhinitis (such as hay fever) (topical form), asthma (inhalation form) for patients unresponsive to less potent corticosteroids, and penile phimosis. In terms of steroid strength, it is more potent than hydrocortisone, and less potent than dexamethasone.
This medication is used to treat skin conditions such as eczema, psoriasis, allergies, andrash. Mometasone decreases swelling (inflammation), itching, and redness. Mometasone is a medium-strength corticosteroid. This medication is available in several forms including cream, ointment, and lotion (solution). Your doctor will choose the type of product based on the skin condition/area of the body being treated.
add to favorites Glutathione CAS 70-18-8 for Skin Care (jerryzhang001@chembj.com) 211100 Other
Glutathione CAS 70-18-8 for Skin Care

Glutathione
Alias:REDUCEDGLUTATHIONE;copren;deltathione;Glutathion;glutathionesh;glutatiol;glutatione;glutide
CAS: 70-18-8
EINECS: 200-725-4
Formula: C20H32N6O12S2
Molecular Weight: 612.63
Appearance: white powder
Content: 99%
Uses: Glutathione is a peptide composed of three amino acids present in almost every cell in the body, especially the liver cells. Protect the liver cell membrane and promote the role of the liver enzyme activity, and many toxic chemicals play a role in detoxification combined. A variety of reasons for liver poisoning, alcoholism caused by the injury, cirrhosis and other diseases have a good effect. Mainly for biochemical reagents, antidotes, mainly for heavy metals, fluoride, carbon monoxide and other toxic organic solvents.

Medical Function:
The Functions of Glutathione are antioxidant, scavenging free radicals, detoxification, enhance immunity, anti-aging, anti-cancer, anti radiation damage, and other functions. It also helps white blood cells to kill bacteria and prevent the oxidation of the vitamins C and E, to prevent stroke and cataract formation. In addition, glutathione can bind the carcinogen, than excrete them through the urine in vitro. 
Enhancing the immune system:
Body' s immune activity, involving unimpeded multiplication of lymphocytes and antibody production, requires maintenance of normal levels of glutathione inside the lymphocytes.

Antioxidant and free radical scavenger:
Glutathione plays a central protective role against the damaging effects of bacteria, viruses, pollutants and free radicals.

Regulator of other antioxidants:
Without glutathione, other important antioxidants such as vitamins C and E cannot do their job adequately to protect your body against disease.

Detoxifying agent:
Another major function of glutathione is in the detoxification of foreign chemical compounds such as carcinogens and harmful metabolites.

Skin whitening:
Dermatologists prescribe Glutathione for its only side effect: Whitening of dark skin. People with darker skin tone report that taking Glutathione capsules along with vitamin C for three to six months or more actually lightens the color of their skin.
add to favorites Phenacetin CAS 62-44-2 as local anesthetic used topically in opthalmology (jerryzhang001@chembj.com) 211100 Other
Phenacetin CAS 62-44-2 as local anesthetic used topically in opthalmology

Phenacetin English Synonyms:
1-ACETYL-P-PHENETIDIN;4-ACETOPHENETIDIDE;4-acetophenetidine;4'-ETHOXYACETANILIDE;4-ETHOXYACETANILIDE;ACETOPHENETIDIN;ACETOPHENETIDINE;ACET-P-PHENETIDINECAS NO.: 62-44-2
EINECS:200-533-0
Assay: 98%
Molecular Formula: C10H13NO2
Molecular Weight: 179.22
Packing: foil bag/tin
Chemical Properties: White crystalline powder
Usage :Analgesic, antipyretic. Component of APC tablets, analgesic mixture also containing aspirin and caffeine. 

Medical Uses:

The antipyretic and analgesic effects of phenacetin are similar to that of acetylsalicylic acid, which is mainly used as anti-inflammatory drugs with a slow and long-lasting effect. It is an effective drug on the treatment of headache, neuralgia, joint pain and fever. However, it has a weak effect on treating anti-rheumatic, anti-inflammatory. Overdose can cause methemoglobinemia, resulting in hypoxia. 
1. Used for organic synthesis of raw materials and drug intermediates from acetaminophen ether. 
2. Antipyretic analgesics for the treatment of fever, headache, neuralgia.
3. Active pharmaceutical ingredient for Scientific Research.
How to Use It?
Overdose can cause methemoglobinemia, resulting in hypoxia. Long-term medication can damage the kidneys, and even cause papillary necrosis, thus it should be taken with caution.
Owing to its side effect and the rapid development of other similar drugs, the drug has been discontinued alone and just used as an active pharmaceutical ingredient for compound preparation with other drugs. It is often combined with aspirin, caffeine, for making aspirin compound (0.162 g of non-phenacetin, 0.227 g of aspirin, and 0.035 g of caffeine) for the treatment of colds with a small toxicity. Further addition of a small amount of the chlorpheniramine can produce chlorpheniramine cold tablets which can be applied to the treatment of colds, headache, neuralgia, rheumatism and so on. 
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