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Merck
모든 사진(1)

주요 문서

41513

Supelco

2-Hexanol

analytical standard

동의어(들):

(±)-2-Hexanol, Butyl methyl carbinol

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About This Item

Linear Formula:
CH3(CH2)3CH(OH)CH3
CAS Number:
Molecular Weight:
102.17
Beilstein:
1718996
EC Number:
MDL number:
UNSPSC 코드:
85151701
PubChem Substance ID:
NACRES:
NA.24

Grade

analytical standard

Quality Level

분석

≥98.0% (GC)

유통기한

limited shelf life, expiry date on the label

refractive index

n20/D 1.414 (lit.)
n20/D 1.415

bp

136 °C (lit.)

density

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

응용 분야

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

형식

neat

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

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일반 설명

2-Hexanol is a volatile aromatic alcohol abundantly occurring in various plant materials. It is often found as a constituent of food and beverages.

애플리케이션

2-Hexanol may be used as an analytical standard for the determination of the analyte in biological samples, fruits, soymilk, food, and aqueous samples by various chromatography techniques.

픽토그램

Flame

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point (°F)

114.8 °F - closed cup

Flash Point (°C)

46 °C - closed cup


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시험 성적서(COA)

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문서 라이브러리 방문

Identification of volatile compounds in soymilk using solid-phase microextraction-gas chromatography
Achouri A, et al.
Food Chemistry, 99(4), 759-766 (2006)
F Schade et al.
Phytochemistry, 56(7), 703-710 (2001-04-21)
Thirteen major volatiles of the carnation flower fragrance signature have been identified by GC/MS. Of these, ten, hexanal, (2E)-hexenal, 1-hexanol, 2-hexanol, 3-hexen-1-ol, nonanal, benzaldehyde, benzyl alcohol, benzyl benzoate and caryophyllene, were quantified. The steady-state levels of these ten volatiles change
John H M Mommers et al.
Journal of chromatography. A, 1182(2), 215-218 (2008-02-02)
A new gas chromatography (GC) method is presented for analysing both the conversion and the enantiomeric excess (e.e.) of samples from alcohol dehydrogenase reactions. The chiral compounds studied were a series of saturated, straight chain alcohols, ranging from 2-butanol to

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