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99% Purity High-Quality Procaine Powder

ID:591024 View:1748 Collection
Date Listed: 2021-07-30 21:50:41 Country: China»Guangdong»Guangzhou
Poster: andy Company: Guangzhou Tengyue Chemical
Location: 1st Ladder 208, Section 8 of Luojia Village, Fuyi Road, Dalong Street, Panyu District, Guangzhou, Guangdong, China, 1st Ladder 307, Section 8 of Luojia Village, Fuyi Road, Dalong Street, Panyu District, Guangzhou, Guangdong, China Website: Guangzhou Tengyue Chemical
Email: andy@tyvovo.com Mobile: 18138708330
Fax: 86-020-84616335 MSN:

English name: PROCAINE CAS No.: 59-46-1 Molecular formula: C13H20N2O2 Molecular weight: 236.31 EINECS number: 200-426-9 Melting point: 61° Boiling point: 378.78 ° C (rough estimate) Payment method: T/T,Western Union,Bitcoins,Money Gram Certification: BP,ISO9001,USP,GMP Customs issues: 100% No customs issues Supply Capacity: 5000kg/1month Appearance: White crystal powder or almost white crystalline powder Packing: 1kg/aluminum foil bag,25kg/cardboard drum or as customers request Delivery: Within 7-9 days Standard: Pharmaceutical Grade Application: Local anesthetic Purity: 99% Uses: Local anesthetics. Its toxicity is low and its effect is fast and safe. It is suitable for local anesthesia and is used in eye, ear, nose and tooth surgery for infiltration anesthesia, conduction anesthesia and closure therapy. This product is also used to produce procaine penicillin. Procaine is an anesthetic agent indicated for production of local or regional anesthesia, particularly for oral surgery. Procaine has the advantage of constricting blood vessels which reduces bleeding, unlike other local anesthetics like lidocaine. Procaine is an ester anesthetic. It is metabolized in the plasma by the enzyme pseudocholinesterase through hydrolysis into para-aminobenzoic acid , which is then excreted by the kidneys into the urine. Procaine acts mainly by inhibiting sodium influx through voltage gated sodium channels in the neuronal cell membrane of peripheral nerves. When the influx of sodium is interrupted, an action potential cannot arise and signal conduction is thus inhibited. The receptor site is thought to be located at the cytoplasmic (inner) portion of the sodium channel. Procaine has also been shown to bind or antagonize the function of N-methyl-D-aspartat receptors as well as nicot

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