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
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:
Already Own This Product?
Find documentation for the products that you have recently purchased in 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