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Rifabutin

Rifabutin is regarded as broad-spectrum antibiotic highly resistant against mycobacteria and Gram-positive bacteria, which can be used alternative medicine for rifampin. The common adverse effects caused by rifabutin are abdominal pain, nausea, rash, headache, and low blood neutrophil levels. This Rifabutin antibiotic working mechanism blocking DNA-dependent RNA polymerase enzyme. Buy Rifabutin online from Hangzhou Hexo Chemtech to get the chemical at the high quality and to avail the chemical in the best online price.

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Rifampicin

Rifampicin which belongs to semisynthetic, broad-spectrum antibiotic and used in combination with antibiotics. Some of the common adverse effects found for rifampicin are nausea, vomiting, diarrhea, and loss of appetite. This antibiotic mechanism of action includes, it inhibits bacterial DNA-dependent RNA synthesis by inhibiting bacterial DNA- dependent RNA polymerase enzyme. Buy Rifampicin online to avail the chemical online at the best price and superior quality. Post your chemical requirements to buy the chemical from the best Rifampicin supplier online.

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Ropivacaine Hydrochloride Ropivacaine Hcl 132112-35-7 Local Anesthetic Raw Material

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Ropivacaine Hydrochloride Ropivacaine Hcl 132112-35-7 Local Anesthetic Raw Material
 
Ropivacaine HCL Basic Info.:
 
Product Name: Ropivacaine hydrochloride
Synonyms: S-ROPIVACAINE HCL;
CAS: 132112-35-7
MF: C17H26N2O.ClH.H2O
MW: 328.88
EINECS: N/A
Product Categories: Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals
use:anesthetic (local),Pharmaceutical raw materials
Packing:Foil bag or as requirments
 
Ropivacaine HCL 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 is an anesthetic (numbing medicine) that blocks the nerve impulses that send pain signals to your brain. 
Ropivacaine is used as a local (in only one area) anesthesia for a spinal block, also called an epidural. The medication is used to provide anesthesia during a surgery or C-section, or to ease labor pains. 
Ropivacaine may also be used for purposes not listed in this medication guide.
 
Ropivacaine HCL Applications:
 
(1) Surgical anesthesia:Epidural anesthesia (including epidural anesthesia during cesarean section);Local infiltration anesthesia.
(2) Acute pain control:For postoperative or labor analgesia continuous epidural infusion can be used can also be intermittent medication;Local infiltration anesthesia.
 

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S4 Most Effective Sarm Supplement Andarine Muscle Building Raw Steroids Powder 401900-40-1

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S4 Most Effective Sarm Supplement Andarine Muscle Building Raw Steroids Powder 401900-40-1
 
Andarine Basic Info:
 
Product name: Andarine
Synonyms: Andarine;S4;S-4;GTX-007
CAS No.: 401900-40-1
MF: C19H18F3N3O6
MW: 441.36
Purity: 99.92%
Product categories APIs; Amines; Aromatics; Chiral Reagents; Intermediates & Fine Chemicals; Pharmaceuticals; SARMS
Appearance: White crystalline powder
Natural Bodybuilding SARM Powder Andarine S4 GTX-007 High Purity CAS 401900-40-1
 
Andarine Description:
 
Selective androgen receptor modulators or SARMs are a novel class of androgen receptor ligands. They are intended to have the same kind of effects as androgenic drugs like anabolic steroids but be much more selective in their action, allowing them to be used for many more clinical indications than the relatively limited legitimate uses that anabolic steroids are currently approved for.
 
S-4 is an experimental or investigation-stage proprietary SARM research chemical developed by GTx Inc for treatment of benign prostatic hypertrophy, muscle wasting, and osteoporosis. S-4 is considered a partial agonist of the androgen receptors in target tissue. S-4 has less pronounced anabolic and androgenic compared to other SARMs. In trials treating BPH induced in animal models, S-4 reduced prostate weight as effectively as finasteride and without producing any reduction in muscle mass or other side effects common with androgen receptor binding compounds. Gao et al suggest that by binding to androgen receptors, S-4 prevents DHT from binding and activating, but bypasses the expected anti-androgenic effects that would occur from occupying androgen receptors due to the fact that S-4 itself is a partial agonist of androgen receptors. S-4 has also been shown to prevent bone loss, reduce body fat, and improve muscle strength and body composition in orchidectomized and ovariectomized rats.
 
Andarine Application:
 
S4 Andarine is an orally active partial agonist for androgen receptors. It is less potent in both anabolic and androgenic effects than other SARMs. In an animal model of benign prostatic hypertrophy, andarine was shown to reduce prostate weight with similar efficacy to finasteride, but without producing any reduction in muscle mass or anti-androgenic side effects.
 
Andarine Function:
 
1. 1/3 as androgenic as testosterone in muscle tissue.
2. Anabolic at doses above 50mg.
3. Great for strength.
4. Great for muscle hardness.
5. Great for enhanced vascularity.
6. Great for endurance (aerobic or anaerobic).
7. Accelerated fat loss above 50mg.
8. Joint healing effects.
 

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Safe Human Growth Hormone Peptide PT 141 Bremelanotide For Peptide Drum PT141 32780-32-8

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Safe Human Growth Hormone Peptide PT 141 Bremelanotide For Peptide Drum PT141 32780-32-8
 
PT 141 Basic Info.
 
Product Name: PT-141; PT141
CAS: 32780-32-8
MF: C50H69N15O10
MW: 1040.17736
Appearance: White powder
Water Content(Karl Fischer): ≤ 5.0%
Acetate Content(by HPLC): ≤ 15.0%
Amino Acid Composition: ± 10% of theoretical
Purity(by HPLC): ≥ 97.0%
Single Impurity(by HPLC): ≤ 1.0%
Peptide Content(by %N): ≥ 80%
Assay(By Anhydrous, Acetic Acid-free): 95.0~105.0%
Bacterial Endotoxins: ≤ 5EU/mg
Grade: Pharmceutical Grade
Storage: Shading, confined preservation
 
PT 141 Description:
 
PT-141 is a synthetic amino acid protein discovered during clinical trials using the Melanotan 2 for sunless tanning, photo-protection results from melanotans. Participants were documented as having experienced aphrodisiac reactions, leading to the further development PT-141. The melanocortin system targets receptors associated with desire through the melanocyte stimulating hormone paths that cross the blood-brain-barrier. Potentially the powerful sex-drug results feeling an aphrodisiac experience amplifying arousal pt141 reviews have shown the ability to increase libido effects of both men and women.
 
PT 141 Application:
 
PT-141 functions by activating the melanocortin receptor and MC4R namely. Bremelanotide originally was tested for nasal spray delivery but was discontinued after concerns about side effects. Bremelanotide PT141, as Melanotan II, may cause spontaneous arousal enhancing effect. Unlike other supplements, PT-141 results do not act on the vascular body, but directly increases desires through the nervous system.
 

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Safety Pure Amino Acid 3,5-Diiodo-L-Thyronine T2 Powder 1041-01-6

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Safety Pure Amino Acid 3,5-Diiodo-L-Thyronine T2 Powder 1041-01-6
 
3,5-Diiodo-L-Thyronine Basic Information:
 
Product Name: 3,5-Diiodo-L-Thyronine
Synonyms: T2;Diiodothyronine;3,5-Diiodo-L-Thyronine;3,5-Diiodothyronine;
CAS: 1041-01-6
MF: C15H13I2NO4
MW: 525.08
EINECS: 213-867-7
Melting point: 255-260°C (dec.)
Storage temp.: 2-8°C
Chemical Properties: Off-White Solid
Product Categories: Medicine intermediate;Amino Acids 13C, 2H, 15N;Amino Acids & Derivatives;Intermediates;Labeling and Diagnostics Reagents
Usage: Of interest for the early detection and treatment of congenital or drug-induced hypothyroidism.
 

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Sarms Powder Steroids Pirfenidone 53179-13-8 Anti Fibrosis

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Sarms Powder Steroids Pirfenidone 53179-13-8 Anti Fibrosis 
 
Pirfenidone Basic information
 
Product Name: Pirfenidone
Synonyms: 5-methyl-1-phenyl-2(1h)-pyridon;amr-69;PIRFENIDONE;5-METHYL-1-PHENYL-1H-PYRIDIN-2-ONE;5-METHYL-1-PHENYL-2(1H)-PYRIDINONE;5-METHYL-1-PHENYL-2-(1H)-PYRIDONE;5-Methyl-N-phenyl-2-1H-pyridone;Pirfenidone also see 5-Methyl-1-Phenyl-2(1H)-Pyridinone
CAS: 53179-13-8
MF: C12H11NO
MW: 185.22
EINECS: N/A
Melting point: 96-97°C
Storage temp.: Store at RT
Solubility: DMSO: ≥10 mg/mL, Soluble
Chemical Properties: Off-White Solid
Usage: Pirfenidone has demonstrated activity in multiple fibrotic conditions, including those of the lung, kidney and liver
Product Categories: Aromatics Compounds;Aromatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Cytokine signaling;Inhibitors.
 
Pirfenidone Description:
 
Pirfenidone (INN, BAN) is an anti-fibrotic drug for the treatment of idiopathic pulmonary fibrosis (IPF). It works by reducing lung fibrosis through downregulation of the production of growth factors and procollagens I and II.
 
It is a drug developed by several companies worldwide, including InterMune Inc. (now part of Roche), Shionogi Ltd., and GNI Group Ltd. In 2008, it was first approved in Japan for the treatment of IPF after clinical trials, under the trade name of Pirespa by Shionogi & Co. In October 2010, the Indian Company Cipla launched it as Pirfenex. In 2011, it was approved for use in Europe for IPF; it was approved in Canada in 2012 ; and was approved in the United States in October 2014 under the same name. In September 2011, the Chinese State Food and Drug Administration provided GNI Group Ltd with new drug approval of pirfenidone in China, and later manufacture approval in 2013 under the trade name of Etuary.
 
In 2014 it was approved in Mexico under the name KitosCell LP, indicated for pulmonary fibrosis and liver fibrosis.There is also a topical form created for the treatment of abnormal wound healing processes.
 
Pirfenidone Application:
 
In vitro, pirfenidone can inhibit the uterine flesh tumour cells and leiomyoma cells proliferation. Pirfenidone can inhibit the TGF - beta - 1 inducing fibroblast collagen formation. Inhibition of PDGF, FGF and TGF - beta - 1 inducing fibroblast proliferation. In hamster model, pirfenidone, taken by mouth, that can the prevention and treatment of pulmonary fibrosis . Pirfenidone can prevent the sclerosing peritonitis in rats induced by chemical, can also be keloid grafting for the treatment of nude mice. Pirfenidone 0.01 1 mg/ml can suppress the matrix and dose dependent manner serum stimulate uterine fibroids and leiomyoma cell DNA synthesis, the compound has no cytotoxic effect, has no effect on collagen mRNA level also. Pirfenidone in hamster pulmonary fibrosis model can reduce the disease before the collagen I mRNA level enhancement, reduce the level of the lung hydroxyproline and malondialadehyde and lung preserved ammonia acyl hydroxylase activity.
 

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Scopine-2,2-dithienyl glycolate

Name   Scopine-2,2-dithienyl glycolate
copyRight
Molecular Structure   CAS # 136310-64-0, Scopine-2,2-dithienyl glycolate
 
Molecular Formula   C18H19NO4S2
Molecular Weight   377.47
CAS Registry Number   136310-64-0

 

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Sell 4CMC, Big Crystal(kaichuang0606@gmail.com)

Product name.: 4-cmc 4-cmc 4-cmc 4-cmc 4-cmc 4-cmc English name: 1-(4-Chlorophenyl)-2-(methylamino)propan-1-one CAS No.: 842212-02-1 Purity: 99.8% Appearance: white big crystal/white transparent big crystal/brown big crystal/Cola color big crystal(new batch) Application: Research purpose Production Capacity: 500 Kilogram/Month Storage:Kept in a cool,dry and ventilated place We also can supply other similars, if you need, contact me back. Email: kaichuang0606@gmail.com Skype: kaichuang0606.

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Serilesine 1

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