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W376205

Sigma-Aldrich

3-Methyl-1-pentanol

≥99%, FG

Synonym(s):

2-ethyl-4-butanol, 3-ethyl-1-butanol, 3-methylpentan-1-ol

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About This Item

Linear Formula:
CH3CH2CH(CH3)CH2CH2OH
CAS Number:
Molecular Weight:
102.17
FEMA Number:
3762
Beilstein/REAXYS Number:
1718979
EC Number:
Council of Europe no.:
10275
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
2.115
NACRES:
NA.21
organoleptic:
chocolate; green; wine-like
grade:
FG
Fragrance grade
Halal
Kosher
biological source:
synthetic
agency:
follows IFRA guidelines
meets purity specifications of JECFA
food allergen:
no known allergens

biological source

synthetic

Quality Level

grade

FG
Fragrance grade
Halal
Kosher

agency

follows IFRA guidelines
meets purity specifications of JECFA

reg. compliance

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002

vapor density

>1 (vs air)

assay

≥99%

refractive index

n20/D 1.418 (lit.)

bp

151-152 °C (lit.)

density

0.823 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

no known allergens

organoleptic

chocolate; green; wine-like

SMILES string

CCC(C)CCO

InChI

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

InChI key

IWTBVKIGCDZRPL-UHFFFAOYSA-N

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General description

3-Methyl-1-pentanol is a fragrance ingredient generally used in shampoos, cosmetics, toilet soaps, and non-cosmetic products like detergents and household cleaners. It is naturally found in the Mangifera species of the mango plant.

pictograms

FlameExclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

140.0 °F - closed cup

flash_point_c

60 °C - closed cup

ppe

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


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A I Pardo-García et al.
Food chemistry, 163, 258-266 (2014-06-11)
The effects of four vine treatments, comprising the application of eugenol and guaiacol (individually or as a mixture) or whiskey lactones on the concentration of glycosidically bound aroma precursors, determined as glycosyl glucose content by HPLC-IR, in Monastrell grapes and

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