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238287

Sigma-Aldrich

1-Iodohexane

contains copper as stabilizer, ≥98%

Synonym(s):

Hexyl iodide

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About This Item

Linear Formula:
CH3(CH2)5I
CAS Number:
638-45-9
Molecular Weight:
212.07
Beilstein:
505971
EC Number:
211-339-0
MDL number:
MFCD00001102
UNSPSC Code:
12352100
PubChem Substance ID:
24854154
NACRES:
NA.22

Quality Level

200

Assay

≥98%

form

liquid

contains

copper as stabilizer

refractive index

n20/D 1.492 (lit.)

bp

179-180 °C (lit.)

density

1.437 g/mL at 25 °C (lit.)

SMILES string

CCCCCCI

InChI

1S/C6H13I/c1-2-3-4-5-6-7/h2-6H2,1H3

InChI key

ANOOTOPTCJRUPK-UHFFFAOYSA-N

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General description

1-Iodohexane undergoes palladium-catalyzed cross-coupling reaction with 9-octyl-9-borabicyclo[3.3.l]nonane to give tetradecane. Thermal reactions of 1-iodohexane on Ni (100) single crystal surfaces has been studied using temperature-programmed desorption and X-ray photoelectron spectroscopy.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

141.8 °F - closed cup

Flash Point(C)

61 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Thermal Reactions of Alkyl Iodides on Ni (100) Single Crystal Surfaces.
Tjandra S and Zaera F.
Journal of the American Chemical Society, 117(38), 9749-9755 (1995)
Palladium-catalyzed carbonylative cross-coupling reaction of iodoalkanes with 9-alkyl-9-BBN derivatives. A direct and selective synthesis of ketones.
Ishiyama T and Miyaura N.
Tetrahedron Letters, 32(47), 6923-6926 (1991)
Martha Kafetzi et al.
Polymers, 13(3) (2021-01-27)
In this work, the synthesis and the aqueous solution self-assembly behavior of novel partially hydrophobically modified poly(2-(dimethylamino) ethyl methacrylate)-b-poly(oligo(ethylelene glycol) methyl ether methacrylatetabel) pH and temperature responsive random diblock copolymers (P(DMAEMA-co-Q6/12DMAEMA)-b-POEGMA), are reported. The chemical modifications were accomplished via quaternization
Barbara Nozière et al.
Angewandte Chemie (International ed. in English), 58(39), 13976-13982 (2019-07-31)
The autoxidation of organic peroxy radicals (RO2 ) into hydroperoxy-alkyl radicals (QOOH), then hydroperoxy-peroxy radicals (HOOQO2 ) is now considered to be important in the Earth's atmosphere. To avoid mechanistic uncertainties these reactions are best studied by monitoring the radicals.
Alexa Schmitz et al.
ChemistryOpen, 10(2), 153-163 (2020-12-24)
S-alkyltetrahydrothiophenium, [Cn THT]+ bis(trifluorosulfonyl)imide, [NTf2 ]- room temperature ionic liquids (ILs) and tetraphenylborate, [BPh4 ]- salts with alkyl chain lengths from C4 to C10 have been prepared. The ILs and salts were characterized and their purity verified by 1 H-
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