Trityl chloride
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Trityl chloride
structure -
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CAS No:
76-83-5
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Formula:
C19H15Cl
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Chemical Name:
Trityl chloride
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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
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CAS No:
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
Ⅲ
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.
Trityl chloride Use and 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.
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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