Basic organic raw materials commonly used in pharm
76-83-5
C19h15cl
200-986-4
Aromatic Hydrocarbon
Medicine Grade
Chlorinated Organic Compounds
Chlorinated Organic Compounds
Chlorinated Organic Compounds
278.78
Powder or Crystal
White to Grayish White or Light Yellow Beige
Cardboard Barrel
Net content: 25kg/ barrel.
China
29036990
Product Description
safety/security information | |
Dangerous goods sign | C,N |
Hazard category code | 34-50/53-14-36/37 |
Safety instructions | 26-36/37/39-45-61-27 |
Dangerous goods transport number | UN 3261 8/PG 3 |
WGK Germany | 3 |
RTECS none | PA6450000 |
F | 10-19-21 |
Hazard Note | Irritant |
TSCA | Yes |
danger classes | 8 |
Packaging category | III |
Customs code | 29036990 |
Toxic substance data | 76-83-5(Hazardous Substances Data) |
toxicity | LD50 orally in Rabbit: > 5000 mg/kg |
Triphenylmethyl chloride is white-like crystal, insoluble in water, easily soluble in benzene, carbon disulfide and petroleum ether, slightly soluble in alcohol and ether, and becomes triphenyl alcohol after water absorption; Melting point of chemical book is 110ºC ~ 112ºC, and boiling point is 230ºC ~ 235ºC (20mmhg). It is an important pharmaceutical intermediate and one of the basic organic raw materials commonly used in pharmaceutical and chemical fields.



1. It is used as an intermediate of cephalosporins to synthesize antiviral drug iodine glycoside. 2, used as amino protective reagent. 3, used as initiator of resin polymer, catalyst of organic reaction, flour improver, fiber decolorant and rubber product exchanger, and also used in the production of medicine and pesticide. 4. Triphenylmethyl chloride is one of the basic organic raw materials commonly used in the field of medicine and chemical industry. It can be used as a selective protective group for primary hydroxyl groups in compounds such as nucleoside, monosaccharide or polysaccharide, and as a basic chemical reagent in polypeptide synthesis. 5. Test the primary alcohol in sugar. Organic synthesis. Triphenylmethylation agent, used for group protection of amines, alcohols and thiols. Used in Wittig reaction to form onium salt. 6, triphenylmethyl reagent

