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Methyl benzenesulfonate

CAS No.
80-18-2
Chemical Name:
Methyl benzenesulfonate
Synonyms
Methyl Besylate;BENZENESULFONIC ACID METHYL ESTER;20ND3-5;nsc06624;ai3-06624;AKOS BBS-00004424;Methyl benzenesulfon;Methylbenzoxysulfonate;METHYL BENZENESULFONATE;Methyl Benzensulfonate
CBNumber:
CB0776273
Molecular Formula:
C7H8O3S
Molecular Weight:
172.2
MDL Number:
MFCD00014737
MOL File:
80-18-2.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-06-24 15:35:27

Methyl benzenesulfonate Properties

Melting point -4 °C
Boiling point 147-150°C 13mm
Density 1.3
refractive index 1.514-1.516
Flash point 143 °C
storage temp. 2-8°C
solubility Chloroform (Sparingly), Methanol (Slightly)
form Liquid
color Clear colorless to slightly yellow
Water Solubility Miscible with chloroform, methanol, ethanol and ether. Immiscible with water.
BRN 908448
InChI 1S/C7H8O3S/c1-10-11(8,9)7-5-3-2-4-6-7/h2-6H,1H3
InChIKey CZXGXYBOQYQXQD-UHFFFAOYSA-N
SMILES COS(=O)(=O)c1ccccc1
CAS DataBase Reference 80-18-2(CAS DataBase Reference)
FDA UNII 69X50842RM
NIST Chemistry Reference Benzenesulfonic acid, methyl ester(80-18-2)
EPA Substance Registry System Benzenesulfonic acid, methyl ester (80-18-2)
UNSPSC Code 41116107
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
Signal word  Danger
Hazard statements  H302-H314-H317
Precautionary statements  P261-P270-P280-P301+P312-P303+P361+P353-P305+P351+P338
PPE Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Hazard Codes  C,Xi
Risk Statements  34-22-43
Safety Statements  28A-26-45-36/37/39
RIDADR  3265
WGK Germany  3
RTECS  DB7151000
Hazard Note  Irritant/Corrosive
TSCA  TSCA listed
HazardClass  8
PackingGroup  III
HS Code  29051990
Storage Class 8A - Combustible corrosive hazardous materials
Hazard Classifications Acute Tox. 4 Oral
Skin Corr. 1B
Skin Sens. 1
REACH Registrations Active
NFPA 704
1
3 0

Methyl benzenesulfonate price More Price(43)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 165956 Methyl benzenesulfonate 98% 80-18-2 100g $148 2026-04-30 Buy
Sigma-Aldrich 165956 Methyl benzenesulfonate 98% 80-18-2 500g $526 2026-04-30 Buy
TCI Chemical B0033 Methyl Benzenesulfonate >98.0%(GC) 80-18-2 25mL $39 2026-04-30 Buy
TCI Chemical B0033 Methyl Benzenesulfonate >98.0%(GC) 80-18-2 100mL $98 2026-04-30 Buy
TRC TRC-M288890-250MG Methyl Benzenesulfonate >95%(HPLC) 80-18-2 250mg $215 2026-06-03 Buy
Product number Packaging Price Buy
165956 100g $148 Buy
165956 500g $526 Buy
B0033 25mL $39 Buy
B0033 100mL $98 Buy
TRC-M288890-250MG 250mg $215 Buy

Methyl benzenesulfonate Chemical Properties,Uses,Production

Description

Methyl benzenesulfonate is used as a raw material for the dye and pharmaceutical industries, used as an alkylating agent in organic synthesis for the production of some synthetic dye. It can also be used for the manufacturing the thin-cation exchanger film.

Preparation

Methyl benzenesulfonate is the effective methylating reagent of synthetic multiple organic intermediate, and industry is at present gone up and mainly adopted Phenylsulfonic acid and methyl alcohol to carry out after the esterification essence to steam, this technology starting material costliness, and reaction time is long, and product yield is low. How to get Methyl benzenesulfonate with high yield, scientists have lots of researcher.

Photolysis

Irradiation of methyl benzenesulfonate in methanol causes photolysis, yielding benzene (5–34%), biphenyl (9–15%), and phenethyl ether (trace amounts). The quantum yield of extinction at a wavelength of 254 nm at room temperature is estimated to be 0.07 ± 0.005 [1].

Genotoxicity

Methyl benzenesulfonate is a sulfonate ester which acts as a potential genotoxic impurity in drug substances. Further, it exerts genotoxic effects in bacterial and mammalian cell systems. Incompatible with strong oxidizing agents, strong acids and strong bases.

Reaction

V. M. Nesterov and I. E. Chubova prepared theobromine from 3-methylxanthine, methyl benzenesulfonate, which has been used as the methylating agent. To obtain theobromine, 3-methylxanthine is generally methylated with dimethyl sulfate in an aqueous ethanolic solution of caustic potash. However, if in the reaction the pH exceeds 8.0, the methylation of 3-methylxanthine leads to caffeine, which forms a by-product.

Chemical Properties

clear colourless to slightly brown liquid

Uses

A sulfonate ester as potential genotoxic impurity in drug substances.

Uses

Methyl benzenesulfonate is a sulfonate ester which acts as a potential genotoxic impurity in drug substances. Further, it exerts genotoxic effects in bacterial and mammalian cell systems.

References

[1] Y. Izawa, Naoki K. (1975). Photolysis of Methyl Benzenesulfonate in Methanol. Bulletin of the Chemical Society of Japan, 48 1, 3197–3199. https://doi.org/10.1246/bcsj.48.3197

77-78-1
71-43-2
80-18-2
Synthesis of Methyl benzenesulfonate from Dimethyl sulfate and Benzene
Global( 356)Suppliers
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Shouguang Nuomeng Chemical Co Ltd. 0536-5399456 13869682027 holly@nuomengchem.com China 47 58
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Alfa Aesar 400-6106006 saleschina@alfa-asia.com China 30103 84
TCI (Shanghai) Development Co., Ltd. 021-67121386 Sales-CN@TCIchemicals.com China 24512 81
Energy Chemical 400-0056266 sales8178@energy-chemical.com China 44850 61
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Accela ChemBio Co.,Ltd. 021-50795510 4000665055 marketing@accelachem.com China 10972 64
Shanghai Longsheng chemical Co.,Ltd. 58099637 13585536065 sales@shlschem.com China 9880 59
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Chemsky(shanghai)International Co.,Ltd. 021-50135380 shchemsky@sina.com China 32273 50

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