Skip to Content
Merck
CN

Key Documents

View All Documentation

195871

6-Methyl-5-hepten-2-ol

99%

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
(CH3)2C=CHCH2CH2CH(OH)CH3
CAS Number:
1569-60-4
Molecular Weight:
128.21
EC Number:
200-838-9
UNSPSC Code:
12352002
PubChem Substance ID:
24851720
Beilstein/REAXYS Number:
1720072
MDL number:
MFCD00004561
Assay:
99%
Form:
liquid
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

assay

99%

form

liquid

refractive index

n20/D 1.448 (lit.)

bp

78 °C/14 mmHg (lit.)

density

0.844 g/mL at 25 °C (lit.)

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

pictograms

Health hazard
GHS08

signalword

Warning

hcodes

H351

Hazard Classifications

Carc. 2

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
SHBH2609V
MKBW8884V
SHBB9916V
SHBB0168V
30996KM

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.

Search for a COA

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
View All Related Papers

Global Trade Item Number

SKUGTIN
195871-25G04061837392290