All Photos(1)
Synonym(s):
tert-Butyl chloride
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
Recommended Products
vapor density
3.2 (vs air)
Quality Level
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
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Related Categories
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.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Liq. 2
WGK
WGK 1
Flash Point(F)
-14.8 °F
Flash Point(C)
-26 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
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’.
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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)
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)
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)
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)
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