All Photos(1)
About This Item
Linear Formula:
(CH3)2C=CHCH2CH2CH(OH)CH3
CAS Number:
Molecular Weight:
128.21
Beilstein/REAXYS Number:
1720072
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
2.124
NACRES:
NA.21
organoleptic:
coriander; green
grade:
FG
biological source:
synthetic
food allergen:
no known allergens
Recommended Products
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
Looking for similar products? Visit Product Comparison Guide
Storage Class
10 - Combustible liquids
wgk_germany
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.
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
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.
A E Janssen et al.
Enzyme and microbial technology, 18(5), 340-346 (1996-04-01)
The fatty acid specificity of lipase from Candida rugosa during the esterification of saturated fatty acids and sulcatol in toluene has been studied. The true kinetic parameters are obtained by fitting the experimental data to a Ping-Pong kinetic model that
Paola Gonzalez Audino et al.
Journal of economic entomology, 98(5), 1506-1509 (2005-12-13)
We report here the identification and behavioral activity of volatile compounds emitted by male Platypus mutatus (=sulcatus) Chapuis while boring galleries in living poplar, Populus deltoides Marshall, trees. Headspace analysis using solid phase microextraction techniques showed the presence of 6-methyl-5-hepten-2-ol
Active Filters
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service
