Skip to Content
Merck
CN

W511404

6-Methyl-5-hepten-2-ol

≥99%, FG

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
(CH3)2C=CHCH2CH2CH(OH)CH3
CAS Number:
Molecular Weight:
128.21
NACRES:
NA.21
Flavis number:
2.124
PubChem Substance ID:
UNSPSC Code:
12164502
MDL number:
Beilstein/REAXYS Number:
1720072
Organoleptic:
coriander; green
Grade:
FG
Biological source:
synthetic
Food allergen:
no known allergens
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


biological source

synthetic

Quality Level

grade

FG

reg. compliance

EU Regulation 1334/2008 & 178/2002

assay

≥99%

refractive index

n20/D 1.448 (lit.)

bp

78 °C/14 mmHg (lit.)

density

0.844 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

coriander; green

SMILES string

CC(O)CC\C=C(\C)C

InChI

1S/C8H16O/c1-7(2)5-4-6-8(3)9/h5,8-9H,4,6H2,1-3H3

InChI key

OHEFFKYYKJVVOX-UHFFFAOYSA-N



Still not finding the right product?

Explore all of our products under 6-Methyl-5-hepten-2-ol


Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

154.4 °F - closed cup

flash_point_c

68 °C - closed cup



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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.

Already Own This Product?

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

Visit the Document Library



Michela Vittorini et al.
Bioprocess and biosystems engineering, 34(2), 247-251 (2010-11-04)
The activity of Thermoanaerobium brockii alcohol dehydrogenase (TBADH) adsorbed on mesoporous silica SBA-15 was compared with that of the free enzyme in water and in biphasic system (water phase up to 50% v/v water). TBADH was active at a water
Shui-Ling Chen et al.
Organic letters, 6(19), 3365-3367 (2004-09-10)
[reaction: see text] A highly efficient chemical kinetic resolution of bishomoallylic alcohols was developed when the alcohols underwent In(OTf)(3)-catalyzed 3,5-oxonium-ene-type cyclization with steroidal aldehyde 2. Consistently high enantiomeric excess (up to >99%) was obtained.
Kenji Mori
Chirality, 23(6), 449-462 (2011-06-03)
Mori's synthetic works on bioactive natural products in general and pheromones in particular started about 40 years ago to establish their absolute configurations and also to clarify their stereochemistry-bioactivity relationships. Results indicate that bioactive natural products are not always enantiomerically