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Merck
CN

186481

6-Bromo-1-hexanol

97%

Synonym(s):

Hexamethylene bromohydrin

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About This Item

Linear Formula:
Br(CH2)6OH
CAS Number:
Molecular Weight:
181.07
UNSPSC Code:
12352200
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1732415
Assay:
97%
Form:
liquid
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Quality Level

assay

97%

form

liquid

reaction suitability

reagent type: cross-linking reagent

refractive index

n20/D 1.482 (lit.)

bp

105-106 °C/5 mmHg (lit.)

density

1.384 g/mL at 25 °C (lit.)

functional group

bromo, hydroxyl

storage temp.

2-8°C

SMILES string

BrCCCCCCO

InChI

1S/C6H13BrO/c7-5-3-1-2-4-6-8/h8H,1-6H2

InChI key

FCMCSZXRVWDVAW-UHFFFAOYSA-N

General description

6-Bromo-1-hexanol, also known as hexamethylene bromohydrin is a cross-linking reagent that is commonly used in organic and polymeric synthesis.

Application

6-Bromo-1-hexanol is used as a cross linker to synthesize cyclic, branched, and bicyclic oligonucleotides by click chemistry. It is also utilized to synthesize gel polymer electrolytes, and polymerizable ionic liquids (PILs) such as 1-[(6-methacryloyloxy)hexyl]3-methylimidazolium bromide.


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter



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Synthesis of Polymerizable Ionic Liquid Monomer and Its Characterization
J Sardar
IOP Conference Series: Materials Science and Engineering, 111, 012021-012021 (2016)
Cycling performance of lithium polymer cells assembled by in situ polymerization of a non-flammable ionic liquid monomer
YS Lee
Electrochimica Acta, 106, 460-464 (2013)
New strategies for cyclization and bicyclization of oligonucleotides by click chemistry assisted by microwaves
J Lietard
The Journal of Organic Chemistry, 73, 191-200 (2008)



Global Trade Item Number

SKUGTIN
186481-5G04061838758163