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213691

Sigma-Aldrich

1,2-Hexanediol

98%

Synonym(s):

1,2-Dihydroxyhexane, 1,2-Hexyleneglycol, 5,6-Dihydroxyhexane, DL-1,2-Hexanediol, Dermasoft Hexiol

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About This Item

Linear Formula:
CH3(CH2)3CH(OH)CH2OH
CAS Number:
6920-22-5
Molecular Weight:
118.17
Beilstein/REAXYS Number:
1719244
EC Number:
230-029-6
MDL number:
MFCD00010737
UNSPSC Code:
12352100
PubChem Substance ID:
24852791
NACRES:
NA.22

Quality Level

200

assay

98%

form

liquid

refractive index

n20/D 1.442 (lit.)

bp

223-224 °C (lit.)

density

0.951 g/mL at 25 °C (lit.)

SMILES string

CCCCC(O)CO

InChI

1S/C6H14O2/c1-2-3-4-6(8)5-7/h6-8H,2-5H2,1H3

InChI key

FHKSXSQHXQEMOK-UHFFFAOYSA-N

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General description

1,2-Hexanediol acts as cosurfactant, used for modifying the sodium dodecyl sulfate micelles. Solubility of 1,2-hexanediol in supercritical CO2 has been reported. It has a tendency of self-association to form micelle-like aggregates.

Application

1,2-Hexanediol can be used in the ruthenium-catalyzed synthesis of oxazolidin-2-ones from urea. It can undergo ruthenium-hydride catalyzed dehydrative coupling with anilines to form substituted indole and quinoline products.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H319

Hazard Classifications

Eye Irrit. 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

251.6 °F - closed cup

flash_point_c

122 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

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(Enantio) selective Hydrogen Autotransfer: Ruthenium?Catalyzed Synthesis of Oxazolidin?2?ones from Urea and Diols.
Pe?a?Lopez M, et al.
Angewandte Chemie (International Edition in English), 55(27), 7826-7830 (2016)
Sooho Yeo et al.
Pharmaceutics, 13(1) (2021-01-01)
Adenosine (AD), which is used for treating wrinkles, exhibits poor skin permeation. The aim of the present study was to develop a cross-linked silicone-based cellulose elastomer as an elastic artificial skin for the treatment of skin wrinkles, a biocompatible lipid-based
Ultrasonic absorption studies of surfactant exchange between micelles and bulk phase in aqueous micellar solutions of nonionic surfactants with short alkyl chains. 1. 1, 2-Hexanediol and 1, 2, 3-octanetriol.
Frindi M, et al.
The Journal of Physical Chemistry, 95(12), 4832-4837 (1991)
Catalytic Synthesis of Substituted Indoles and Quinolines from the Dehydrative C?H Coupling of Arylamines with 1, 2-and 1, 3-Diols.
Lee H and Yi C S
Organometallics, 35(11), 1973-1977 (2016)
Carina Waldner et al.
Materials (Basel, Switzerland), 13(12) (2020-06-21)
Ultrasonic liquid penetration (ULP) measurements of porous sheets have been applied for a variety of purposes ranging from determining liquid absorption dynamics to surface characterization of substrates. Interpretation of ULP results, however, is complex as the ultrasound signal can be
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