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240540

Sigma-Aldrich

Benzoyl chloride

ReagentPlus®, ≥99%

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About This Item

Linear Formula:
C6H5COCl
CAS Number:
98-88-4
Molecular Weight:
140.57
Beilstein:
471389
EC Number:
202-710-8
MDL number:
MFCD00000653
UNSPSC Code:
12352100
PubChem Substance ID:
24854420

vapor density

4.88 (vs air)

vapor pressure

1 mmHg ( 32 °C)

product line

ReagentPlus®

Assay

≥99%

autoignition temp.

1056 °F

expl. lim.

4.9 %

refractive index

n20/D 1.553 (lit.)

bp

198 °C (lit.)

mp

−1 °C (lit.)

density

1.211 g/mL at 25 °C (lit.)

SMILES string

ClC(=O)c1ccccc1

InChI

1S/C7H5ClO/c8-7(9)6-4-2-1-3-5-6/h1-5H

InChI key

PASDCCFISLVPSO-UHFFFAOYSA-N

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Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 1

Flash Point(F)

161.6 °F - closed cup

Flash Point(C)

72 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
61697MJV
STBB5977V
STBB5977
S77794
61697MJ

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Solid catalyst treated with anion: XVIII. Benzoylation of toluene with benzoyl chloride and benzoic anhydride catalysed by solid superacid of sulfate-supported alumina.
Arata K and Hino M.
Applied Catalysis, 59(1), 197-204 (1990)
High activity of iron containing metal-organic-framework in acylation of p-xylene with benzoyl chloride.
Kurfirtova L, et al.
Catalysis Today, 179(1), 85-90 (2012)
An unexpected silver triflate-catalyzed reaction of 2-alkynylbenzaldoxime in the presence of benzoyl chloride.
Liu G, et al.
Royal Society of Chemistry Advances, 3(27), 10666-10668 (2013)
Adem Asan et al.
Journal of chromatography. A, 988(1), 145-149 (2003-03-22)
A simple reversed-phase LC method capable of detecting ng/ml quantities of phenolic compounds in water is described. Pre-column derivatization with benzoyl chloride is used for the separation and determination o-cresol, m-cresol, p-cresol, phenol, resorcinol, catechol and hydroquinone in water. The
P Campos-Rey et al.
The journal of physical chemistry. B, 114(44), 14004-14011 (2010-10-20)
The solvolysis of substituted benzoyl chlorides is sensitive both to substituent electronic effects and to medium effects. The solvolysis reactions of substituted benzoyl chlorides have been analyzed in the presence of nonionic micelles. The reaction is inhibited or catalyzed depending
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