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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

Quality Level

100

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 Classifications

Aquatic Acute 1 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

EU REACH Annex XVII (Restriction List)

CAS No.

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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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

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