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476447

Sigma-Aldrich

1-Iodo-3-methylbutane

97%

Synonym(s):

Isoamyl iodide, Isopentyl iodide

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About This Item

Linear Formula:
(CH3)2CHCH2CH2I
CAS Number:
541-28-6
Molecular Weight:
198.05
Beilstein:
1730990
EC Number:
208-773-8
MDL number:
MFCD00039414
UNSPSC Code:
12352100
PubChem Substance ID:
24871256
NACRES:
NA.22

Assay

97%

refractive index

n20/D 1.492 (lit.)

bp

149 °C (lit.)

density

1.497 g/mL at 25 °C (lit.)

SMILES string

CC(C)CCI

InChI

1S/C5H11I/c1-5(2)3-4-6/h5H,3-4H2,1-2H3

InChI key

BUZZUHJODKQYTF-UHFFFAOYSA-N

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Related Categories

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226,H302

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

104.0 °F

Flash Point(C)

40 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Vibrational analysis of alkyl iodides: 1-iodo-2-methylpropane and 1-iodo-3-methylbutane.
Crowder GA and Jalilian MR .
Journal of Molecular Structure, 49(2), 287-292 (1978)
Ultrasound mediated synthesis of a few naturally occurring compounds.
Singh J, et al.
Indian J. Chem. B, 40(5), 386-390 (2001)
The far ultra-violet spectra of some branched chain iodo-alkanes, iodo-cyclo-alkanes, fluoro-iodo-alkanes and iodo-alkenes.
Boschi RA and Salahub DR.
Molecular Physics, 24(4), 735-752 (1972)
Ketoreductases in the synthesis of valuable chiral intermediates: application in the synthesis of α-hydroxy β-amino and β-hydroxy γ-amino acids.
Kambourakis S and Rozzell JD.
Tetrahedron, 60(3), 663-669 (2004)

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