Skip to Content
Merck
All Photos(2)

Documents

541486

Sigma-Aldrich

2,6-Dimethyl-4-heptanol

80%

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
CH3CH(CH3)CH2CH(OH)CH2CH(CH3)CH3
CAS Number:
108-82-7
Molecular Weight:
144.25
EC Number:
203-619-6
MDL number:
MFCD00008944
UNSPSC Code:
12352100
PubChem Substance ID:
24878539
NACRES:
NA.22

Assay

80%

refractive index

n20/D 1.423 (lit.)

bp

178 °C (lit.)

density

0.809 g/mL at 25 °C (lit.)

SMILES string

CC(C)CC(O)CC(C)C

InChI

1S/C9H20O/c1-7(2)5-9(10)6-8(3)4/h7-10H,5-6H2,1-4H3

InChI key

HXQPUEQDBSPXTE-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

2,6-Dimethyl-4-heptanol may be used in the preparation of the protected β-hydroxybutyrates. It may also be used as a hydrogen donor during the dynamic kinetic resolution (DKR) of various diols, monoprotected diols and the protected hydroxy aldehydes.

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

150.8 °F - closed cup

Flash Point(C)

66 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Customers Also Viewed

Slide 1 of 2

1 of 2

2,4-Dimethyl-3-pentanol 99%

Sigma-Aldrich

150045

2,4-Dimethyl-3-pentanol

2-Ethyl-1-hexanol ≥99.6%

Sigma-Aldrich

538051

2-Ethyl-1-hexanol

Lipase/ruthenium-catalyzed dynamic kinetic resolution of hydroxy acids, diols, and hydroxy aldehydes protected with a bulky group.
M J Kim et al.
The Journal of organic chemistry, 66(13), 4736-4738 (2001-06-26)
Mahn Joo Kim et al.
Current opinion in biotechnology, 13(6), 578-587 (2002-12-17)
The combination of enzyme and metal catalysis is described as a useful method for the synthesis of optically active compounds. A key feature of this new methodology is the use of metal catalysts for the in situ racemization of enzymatically
Dynamic kinetic resolution of secondary alcohols by enzyme?metal combinations in ionic liquid.
Kim MJ, et al.
Green Chemistry, 6(9), 471-474 (2004)

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