Skip to Content
MilliporeSigma
Get 22% off for Pi Day through March 31.Save Now

128570

2-Hexanol

99%

Synonym(s):

(±)-2-Hexanol, Butyl methyl carbinol

Slide 1 of 3
Sign In to View Organizational & Contract Pricing.

Select a Size

25 G

$101.00

100 G

$377.00

$101.00

Check Cart for Availability
​
Request a Bulk Order
​
Ships Every 4 weeks

About This Item

Linear Formula:
CH3(CH2)3CH(OH)CH3
CAS Number:
626-93-7
Molecular Weight:
102.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24847868
EC Number:
210-971-4
Beilstein/REAXYS Number:
1718996
MDL number:
MFCD00004585
Assay:
99%
Form:
liquid

Key Documents

View All Documentation

Skip To

Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Quality Level

100

assay

99%

form

liquid

refractive index

n20/D 1.414 (lit.)

bp

136 °C (lit.)

density

0.814 g/mL at 20 °C, 0.81 g/mL at 25 °C (lit.)

functional group

hydroxyl

SMILES string

CCCCC(C)O

InChI

1S/C6H14O/c1-3-4-5-6(2)7/h6-7H,3-5H2,1-2H3

InChI key

QNVRIHYSUZMSGM-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Compare Similar Items

View Full Comparison

Show Differences

1 of 3

This Item
PHR3275W256714
2-Hexanol 99%

Sigma-Aldrich

128570

2-Hexanol

n-Hexanol certified reference material, pharmaceutical secondary standard

Supelco

PHR3275

n-Hexanol

Hexyl alcohol natural, ≥98%, FCC, FG

Sigma-Aldrich

W256714

Hexyl alcohol

assay

99%

assay

-

assay

≥98%

Quality Level

100

Quality Level

300

Quality Level

400

refractive index

n20/D 1.414 (lit.)

refractive index

n20/D 1.418 (lit.)

refractive index

n20/D 1.418 (lit.)

density

0.814 g/mL at 20 °C, 0.81 g/mL at 25 °C (lit.)

density

0.814 g/mL at 25 °C (lit.)

density

0.814 g/mL at 25 °C (lit.)

bp

136 °C (lit.)

bp

156-157 °C (lit.)

bp

156-157 °C (lit.)

form

liquid

form

-

form

liquid

General description

2-Hexanol is one of the constituent of Porella arboris-vitae extracts which has been determined by solid phase microextraction, gas chromatography-mass spectrometry (SPME GC-MS)[1].

pictograms

Flame
GHS02

signalword

Warning

hcodes

H226

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

114.8 °F - closed cup

flash_point_c

46 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SHBT3263
SHBS4613
SHBS2056
SHBR1754
SHBR1753

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Amit Kumar Tyagi et al.
Evidence-based complementary and alternative medicine : eCAM, 2013, 382927-382927 (2013-02-01)
The chemical composition of Porella arboris-vitae extracts was determined by solid phase microextraction, gas chromatography-mass spectrometry (SPME GC-MS), and 66 constituents were identified. The dominant compounds in methanol extract of P. arboris-vitae were β-caryophyllene (14.7%), α-gurjunene (10.9%), α-selinene (10.8%), β-elemene
Kenji Gomi et al.
Plant molecular biology, 53(1-2), 189-199 (2004-02-06)
An expression profile of genes induced by non-pathogenic Alternaria alternata on rough lemon leaves was obtained by sequencing 500 subtractive PCR clones generated from mRNA of leaves inoculated with the fungus after subtraction with that of non-inoculated leaves. About 6%
S J Crosbie et al.
Human & experimental toxicology, 16(3), 131-137 (1997-03-01)
1. The in vitro metabolism of n-hexane was studied in rat liver, lung, brain and skeletal muscle microsomes and in microsomes prepared from cell lines expressing human cytochrome P-450 2E1 or 2B6. The hydroxylated metabolites of n-hexane were quantified by
Zhi-Xia Zheng et al.
Electrophoresis, 25(18-19), 3263-3269 (2004-10-09)
A novel chiral microemulsion, which involved the use of chiral alcohols as cosurfactants, was demonstrated for the enantiomeric separation of a number of pharmaceutical drugs in microemulsion electrokinetic chromatography (MEEKC). The chiral alcohols investigated were optically active 2-alkanols, with the
B Mortensen et al.
Pharmacology & toxicology, 81(1), 35-41 (1997-07-01)
In vitro systems of high biological organization, e.g. containing intact hepatocytes, have been considered as more reliable for metabolic studies and in vivo predictions of toxicokinetics than subcellular systems. For this reason, the kinetics and metabolism of low-molecular-weight volatile chemicals
View All Related Papers

Global Trade Item Number

SKUGTIN
128570-100G04061838725721
128570-25G04061838725738

Questions

Reviews

No rating value

Active Filters

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