Skip to Content
Merck
All Photos(1)

Documents

238287

Sigma-Aldrich

1-Iodohexane

contains copper as stabilizer, ≥98%

Synonym(s):

Hexyl iodide

Sign Into View Organizational & Contract Pricing
All Photos(1)

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

Looking for similar products? Visit Product Comparison Guide

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)

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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-
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service