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245798

Sigma-Aldrich

2-Iodo-2-methylpropane

contains copper as stabilizer, 95%

Synonym(s):

tert-Butyl iodide

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About This Item

Linear Formula:
(CH3)3Cl
CAS Number:
558-17-8
Molecular Weight:
184.02
Beilstein:
505950
MDL number:
MFCD00001068
UNSPSC Code:
12352100
PubChem Substance ID:
24854758
NACRES:
NA.22

Assay

95%

form

liquid

contains

copper as stabilizer

refractive index

n20/D 1.491 (lit.)

bp

99-100 °C (lit.)

mp

−38 °C (lit.)

density

1.544 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)I

InChI

1S/C4H9I/c1-4(2,3)5/h1-3H3

InChI key

ANGGPYSFTXVERY-UHFFFAOYSA-N

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General description

2-Iodo-2-methylpropane was degraded by reductive dehalogenation with nickel-aluminum alloy in potassium hydroxide solution.

Signal Word

Danger

Hazard Statements

H225,H302,H315,H319,H400

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Michael H Abraham et al.
Physical chemistry chemical physics : PCCP, 23(5), 3311-3320 (2021-02-03)
We have obtained properties (or descriptors) of the transition states in the solvolysis of tert-butyl chloride, bromide and iodide. We show that all three transition states, in both protic and in aprotic solvents, are highly dipolar and are strong hydrogen
G Lunn et al.
American Industrial Hygiene Association journal, 52(6), 252-257 (1991-06-01)
Two techniques were investigated for degrading a number of halogenated compounds of commercial and research importance. Reductive dehalogenation with nickel-aluminum alloy in potassium hydroxide solution was used to degrade iodomethane, chloroacetic acid, trichloroacetic acid, 2-chloroethanol, 2-bromoethanol, 2-chloroethylamine, 2-bromoethylamine, 1-bromobutane, 1-iodobutane
Viktor P Bogdanov et al.
Chemistry, an Asian journal, 15(11), 1701-1708 (2020-04-16)
Alkylation of homofullerene [6,6]-C60 (CF2 )2- dianion with the set of alkyl halides, RX, was established to demonstrate an effect of RX nature on the conversion, product composition, and regioselectivity. The respective C60 (CF2 )RH, C60 (CF2 )R2 and C60

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