Acetyl chloride, 98%
Acetyl chloride, 98%
Acetyl chloride, 98%
Acetyl chloride, 98%
Thermo Scientific Chemicals

Acetyl chloride, 98%

CAS: 75-36-5 | C2H3ClO | 78.50 g/mol
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500 mL
25 mL
Catalog number ALFL14013.AP
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500 mL
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Specifications
Chemical Name or MaterialAcetyl chloride
CAS75-36-5
Health Hazard 1H225-H314
Health Hazard 2GHS H Statement
H225-H314
Highly flammable liquid and vapor.
Causes severe skin burns and eye damage.
Health Hazard 3P210-P233-P235-P240-P241-P242-P243-P260-P264b-P271-P280-P284-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P370+P378q-P501c
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Acetyl chloride acts as a reagent for the preparation of esters and amides of acetic acid. It is also useful as an important reactant in Friedel-Crafts reactions as well as in the introduction of an acetyl group. It serves as a starting material in the production of pharmaceutical, new plating complexing agent, acylation agent and synthetic organic intermediates.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Acetyl chloride acts as a reagent for the preparation of esters and amides of acetic acid. It is also useful as an important reactant in Friedel-Crafts reactions as well as in the introduction of an acetyl group. It serves as a starting material in the production of pharmaceutical, new plating complexing agent, acylation agent and synthetic organic intermediates.

Solubility
Miscible with acetone, chloroform, glacial acetic acid, petroleum ether, ether and benzene.

Notes
Moisture sensitive. Incompatible with water, alcohols, oxidizing agents and strong bases.
RUO – Research Use Only

General References:

  1. Indorkar, D.; Chourasia, O. P.; Limaye, S. N. Synthesis and Characterization of some new Synthesis of 1-acetyl-3-(4-nitrophenyl)-5-(substituted phenyl) pyrazoline Derivative and antimicrobial activity. Int. J. Curr. Microbiol. App. Sci. 2015, 4 (2), 670-678.
  2. Pijper, T. C.; Robertus, J.; Browne, W. R.; Feringa, B. L. Mild Ti-mediated transformation of t-butyl thio-ethers into thio-acetates. Org. Biomol. Chem. 2015, 13 (1), 265-268.