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128570

Sigma-Aldrich

2-Hexanol

99%

Synonym(e):

(±)-2-Hexanol, Butyl-methylcarbinol

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About This Item

Lineare Formel:
CH3(CH2)3CH(OH)CH3
CAS-Nummer:
626-93-7
Molekulargewicht:
102.17
Beilstein:
1718996
EG-Nummer:
210-971-4
MDL-Nummer:
MFCD00004585
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24847868
NACRES:
NA.22

Qualitätsniveau

100

Assay

99%

Form

liquid

Brechungsindex

n20/D 1.414 (lit.)

bp

136 °C (lit.)

Dichte

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

Funktionelle Gruppe

hydroxyl

SMILES String

CCCCC(C)O

InChI

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

InChIKey

QNVRIHYSUZMSGM-UHFFFAOYSA-N

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Allgemeine Beschreibung

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).

Piktogramme

Flame
GHS02

Signalwort

Warning

H-Sätze

H226

Gefahreneinstufungen

Flam. Liq. 3

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 1

Flammpunkt (°F)

114.8 °F - closed cup

Flammpunkt (°C)

46 °C - closed cup

Persönliche Schutzausrüstung

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

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
SHBN1139
SHBH9898
SHBC3835V
SHBB6478V
80396HMV

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2-Nonanol 99%

Sigma-Aldrich

N30307

2-Nonanol

1-Hexanol for synthesis

Sigma-Aldrich

8.04393

1-Hexanol

2-Hexanon reagent grade, 98%

Sigma-Aldrich

103004

2-Hexanon

Isopentylacetat mixture of isomers, reagent grade, 98%

Sigma-Aldrich

112674

Isopentylacetat

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
P Manini et al.
Toxicology letters, 108(2-3), 225-231 (1999-10-08)
Since n-hexane metabolites are excreted as glucuronide conjugates, most conventional analytical procedures require preliminary hydrolysis, yielding to the 'total' 2,5-hexanedione (2,5-HD), but also giving rise to a number of artifacts. The whole pattern of n-hexane metabolites, both conjugated and unconjugated
Christina Onaca et al.
Journal of bacteriology, 189(10), 3759-3767 (2007-03-14)
Pseudomonas veronii MEK700 was isolated from a biotrickling filter cleaning 2-butanone-loaded waste air. The strain is able to grow on 2-butanone and 2-hexanol. The genes for degradation of short chain alkyl methyl ketones were identified by transposon mutagenesis using a
M Sakura et al.
Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology, 188(10), 787-797 (2002-12-06)
The capability of the cockroach Periplaneta americana to discriminate odors of structurally similar aliphatic alcohols was studied by using an operant conditioning paradigm. Cockroaches were trained to discriminate three odors: one odor associated with sucrose solution (reward) and two odors
S J Crosbie et al.
Human & experimental toxicology, 16(3), 138-145 (1997-03-01)
1. The role of skeletal muscle microsomes as a site of extrahepatic xenobiotic metabolism using n-hexane as a model substrate was investigated. The observed cytochrome P450-dependent metabolism was compared with that found with liver, and brain microsomal fractions. 2. Rat
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