p-Toluoyl chloride
p-Toluoyl chloride
  • CAS No.:874-60-2
Other grades of this product :
p-Toluoyl chloride Basic information
Product Name:p-Toluoyl chloride
Synonyms:4-methylbenzoicacidchloride;4-methyl-benzoylchlorid;Benzoyl chloride, 4-methyl-;p-Toluoyl chlori;p-Toluoyl chloride 98%;The Methyl benzoyl chloride;P-methbenzoylchloride;4-Methylbenzenecarbonyl chloride
CAS:874-60-2
MF:C8H7ClO
MW:154.59
EINECS:212-864-8
Product Categories:Acid Halides;Building Blocks;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks;Pyridines;ACIDHALIDE;874-60-2
Mol File:874-60-2.mol
p-Toluoyl chloride Chemical Properties
Melting point -4--2 °C (lit.)
Boiling point 225-227 °C (lit.) 95-96 °C/10 mmHg (lit.)
density 1.169 g/mL at 25 °C (lit.)
vapor density 5.33 (vs air)
vapor pressure 0.55 mm Hg ( 20 °C)
refractive index n20/D 1.553(lit.)
Fp 180 °F
storage temp. Store below +30°C.
form Liquid
Specific Gravity1.169
color Clear colorless to slightly brown
PH1 (H2O, 20℃)
explosive limit1.6%, 117°F
Water Solubility Reacts with water alcohol.
Sensitive Moisture Sensitive
BRN 471492
CAS DataBase Reference874-60-2(CAS DataBase Reference)
NIST Chemistry Reference4-Methylbenzoic acid chloride(874-60-2)
EPA Substance Registry SystemBenzoyl chloride, 4-methyl- (874-60-2)
Safety Information
Hazard Codes C
Risk Statements 34
Safety Statements 26-36/37/39-45-24/25
RIDADR UN 3265 8/PG 2
WGK Germany 3
RTECS XV1660000
TSCA Yes
HazardClass 8
PackingGroup II
HS Code 29163900
MSDS Information
ProviderLanguage
4-Methylbenzoyl chloride English
SigmaAldrich English
ACROS English
ALFA English
p-Toluoyl chloride Usage And Synthesis
Chemical PropertiesCLEAR COLOURLESS TO SLIGHTLY BROWNISH LIQUID
Usesp-Toluoyl chloride was used to prepare antigen, Tolyl-amido-human serum albumin
Usesp-Toluoyl chloride was used to prepare antigen, Tolyl-amido-human serum albumin. It is used as a reagent to synthesize (+)-Yashabushitriol, derivatives of Desloratadine.
UsesIntermediates of Liquid Crystals
General Descriptionp-Toluoyl chloride causes the benzoylation of toluene using triflic acid funtionalized mesoporous Zr-TMS catalysts. It causes1,9-diacylation of a dipyrromethane using the hindered Grignard reagent 2,6-dimethylphenylmagnesium bromide.

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