Skip to Content
Merck
All Photos(1)

Key Documents

T72605

Sigma-Aldrich

Trimethylacetyl chloride

99%

Synonym(s):

Pivaloyl chloride, Trimethylacetyl chloride

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(CH3)3CCOCl
CAS Number:
Molecular Weight:
120.58
Beilstein:
385668
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

>1 (vs air)

Quality Level

vapor pressure

36 mmHg ( 20 °C)

Assay

99%

refractive index

n20/D 1.412 (lit.)

bp

105-106 °C (lit.)

density

0.979 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)C(Cl)=O

InChI

1S/C5H9ClO/c1-5(2,3)4(6)7/h1-3H3

InChI key

JVSFQJZRHXAUGT-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Widely used N-acylating agent for amines, Schiff bases, and pyrrolidinones as well as O-acylating agent for alcohols, lactones, and saccharides.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Met. Corr. 1 - Skin Corr. 1B

Supplementary Hazards

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

55.4 °F - closed cup

Flash Point(C)

13 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Tetrahedron, 49, 599-599 (1993)
The Journal of Organic Chemistry, 59, 1703-1703 (1994)
D Becker et al.
Carbohydrate research, 248, 129-141 (1993-10-04)
A new method has been developed for preparation of partially pivaloylated saccharides in one step from readily available starting materials. These intermediates were used in the synthesis of disaccharides and a glucosteroid.
Journal of Carbohydrate Chemistry, 12, 841-841 (1993)
Angewandte Chemie (International Edition in English), 32, 72-72 (1993)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service