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Trityl chloride

Trityl chloride structure

Trityl chloride 

structure
  • CAS No:

    76-83-5

  • Formula:

    C19H15Cl

  • Chemical Name:

    Trityl chloride

  • Synonyms:

    Benzene,1,1′,1′′-(chloromethylidyne)tris-;Methane,chlorotriphenyl-;1,1′,1′′-(Chloromethylidyne)tris[benzene];Chlorotriphenylmethane;Triphenylchloromethane;Triphenylmethyl chloride;Trityl chloride;NSC 435;(Chlorodiphenylmethyl)benzene;(Chloromethanetriyl)tribenzene

  • Categories:

    Biochemical Engineering  >  Amino Acids and Derivatives

Description

White to yellow solid

Trityl chloride Basic Attributes

278.78

278.78

397363

200-986-4

1D9GZ8QQXN

435

DTXSID3052511

NEEDLES OR PRISMS FROM BENZENE OR PETROLEUM ETHER

29036990

Characteristics

0

5

White to off-white or light yellow-beige Powder or Crystals

1.1±0.1 g/cm3

113-114 °C

310 °C @ Press: 760 Torr

230-235°C/20mm

1.608

Insoluble in water. soluble in chloroform, hexane, benzene, ether, acetone and tetrahydrofuran.chloroform: 0.1 g/mL, clear

StoreunderNitrogen

LD50 orally in Rabbit: > 5000 mg/kg

DECOMP IN HOT WATER & ALCOHOL

Safety Information

8

UN 3261 8/PG 3

3

34-50/53-14-36/37

26-36/37/39-45-61-27

PA6450000

C,N

Irritant

Stable at room temperature in closed containers under normal storage and handling conditions.

P280-P305 + P351 + P338-P310

H314

|Danger|H314 (67.02%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]|P260, P261, P264, P271, P273, P280, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P332+P313, P362, P363, P391, P403+P233, P405, and P501|Aggregated GHS information provided by 94 companies from 10 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Toxicity

426.58

Drug Information

0.71 Days

triphenylmethylchloride

Trityl chloride Use and Manufacturing

Methods of Manufacturing

Dry thiophene-free benzene and carbon tetrachloride are mixed and cooled to 0-5°C, aluminum trichloride is added, and a large amount of hydrogen chloride gas is released during the stirring reaction. The reactant is added to the pre-cooled mixture of benzene and hydrochloric acid, and hydrolyzed below 25°C. After the reaction, the benzene layer was separated. Heat and distill off benzene, cool to 40℃, add a little acetyl chloride, and heat to reflux for a while. After cooling, the mother liquor is filtered off, the filter cake is washed once with petroleum ether and benzene, and dried to obtain triphenylchloromethane.

Uses

Efficient method of tritylation of sensitive compounds and their subsequent detritylation

Benzene, 1,1',1''-(chloromethylidyne)tris-: ACTIVE|TRIARYL CHLOROALKANE IMPROVED ADHESION OF FAST-SETTING POLYURETHANE PREPOLYMER TO TISSUE.

Computed Properties

Molecular Weight:278.8
XLogP3:5
Rotatable Bond Count:3
Exact Mass:278.0862282
Monoisotopic Mass:278.0862282
Heavy Atom Count:20
Complexity:235
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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