Skip to Content
Merck
All Photos(1)

Documents

C56352

Sigma-Aldrich

2-Chloro-2-methylpropane

99%

Synonym(s):

tert-Butyl chloride

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(CH3)3CCl
CAS Number:
Molecular Weight:
92.57
Beilstein:
1730872
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

3.2 (vs air)

vapor pressure

4.82 psi ( 20 °C)

Assay

99%

form

liquid

refractive index

n20/D 1.385 (lit.)

bp

51-52 °C (lit.)

mp

−25 °C (lit.)

density

0.851 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)Cl

InChI

1S/C4H9Cl/c1-4(2,3)5/h1-3H3

InChI key

NBRKLOOSMBRFMH-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

  • 2-Chloro-2-methylpropane is an alkylating agent that is used to functionalize molecules with tert-butyl group.
  • It serves as an effective chlorinating agent, in combination with the ionic liquid, 1-butyl-3-methylimidazolium bromide for converting alcohols into chlorides.
  • It can also be used to prepare tert-butyl ethers by treating with corresponding alcohols.

Pictograms

Flame

Signal Word

Danger

Hazard Statements

Hazard Classifications

Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

-14.8 °F - closed cup

Flash Point(C)

-26 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Improved procedure for preparation of t-alkyl aryl ethers.
Camps F, et al.
Synthesis, 03, 186-188 (1982)
Direct Halogenation of Alcohols and Their Derivatives with tert?Butyl Halides in the Ionic Liquid [pmIm]Br under Sonication Conditions?A Novel, Efficient and Green Methodology.
Ranu B C and Jana R
European Journal of Organic Chemistry, 2005(4), 755-758 (2005)
Synthesis and characterization of teranthene: a singlet biradical polycyclic aromatic hydrocarbon having Kekule structures.
Konishi A, et al.
Journal of the American Chemical Society, 132(32), 11021-11023 (2010)
Pyrene?Based Y?shaped Solid?State Blue Emitters: Synthesis, Characterization, and Photoluminescence.
Feng X, et al.
Chemistry - An Asian Journal, 7(12), 2854-2863 (2012)
Palladium-Catalyzed Cyclization: Regioselectivity and Structure of Arene-Fused C60 Derivatives.
Hashikawa Y, et al.
Journal of the American Chemical Society, 139(45), 16350-16358 (2017)

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