Skip to Content
MilliporeSigma
All Photos(1)

Documents

464465

Sigma-Aldrich

2-Butyl-1-octanol

95%

Synonym(s):

2-Butyloctanol, 2-Butyloctyl alcohol, 5-(Hydroxymethyl)undecane, Butyloctanol, Guerbet dodecanol

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
CH3(CH2)5CH[(CH2)3CH3]CH2OH
CAS Number:
3913-02-8
Molecular Weight:
186.33
EC Number:
223-470-0
MDL number:
MFCD00053508
UNSPSC Code:
12352100
PubChem Substance ID:
24870183
NACRES:
NA.22

assay

95%

bp

145-149 °C (lit.)

density

0.833 g/mL at 25 °C (lit.)

SMILES string

CCCCCCC(CO)CCCC

InChI

1S/C12H26O/c1-3-5-7-8-10-12(11-13)9-6-4-2/h12-13H,3-11H2,1-2H3

InChI key

XMVBHZBLHNOQON-UHFFFAOYSA-N

General description

2-Butyl-1-octanol (BuOA) is a long-chain glass forming monohydroxy alcohol.

Application

2-Butyl-1-octanol (BuOA) has been used to synthesize:
  • 2-butyl-1-octyl-methacrylate (BOMA)
  • 3,5,5-trimethyl-1-hexyl methacrylate (TMHMA)
  • hydrophobic polyesters in miniemulsion in the presence of large amounts of water

It has also been used as an extraction solvent in extractive fed-batch experiments.

pictograms

Environment
GHS09

signalword

Warning

hcodes

H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

10 - Combustible liquids

wgk_germany

WGK 2

flash_point_f

251.6 °F - Non-equilibrium method

flash_point_c

122 °C - Non-equilibrium method

ppe

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

Helena González-Peñas et al.
Biotechnology letters, 37(3), 577-584 (2014-10-30)
Acetone/butanol/ethanol (ABE) fermentation by Clostridium acetobutylicum was investigated in extractive fed-batch experiments. In conventional fermentations, metabolic activity ceases when a critical threshold products concentration is reached (~21.6 g solvents l(-1)). Solvents production was increased up to 36.6 and 37.2 g
Polyester synthesis in aqueous miniemulsion.
Barrere M and Landfester K.
Polymer, 44(10), 2833-2841 (2003)
Gergely Kali et al.
Langmuir : the ACS journal of surfaces and colloids, 23(21), 10746-10755 (2007-09-11)
Seven amphiphilic conetworks of methacrylic acid (MAA) and a new hydrophobic monomer, 2-butyl-1-octyl-methacrylate (BOMA), were synthesized using group transfer polymerization. The MAA units were introduced via the polymerization of tetrahydropyranyl methacrylate (THPMA) followed by the removal of the protecting tetrahydropyranyl
Liping Kong et al.
Bioresource technology, 299, 122582-122582 (2019-12-27)
Direct hydrogenolysis of Kraft lignin was catalyzed over a series of supported Ni or Re catalysts in ethanol solvent. The best results showed that the oil yield of 96.70 wt% was obtained with less char formation at 330 °C for 3 h over
Yanqin Gao et al.
The Journal of chemical physics, 139(16), 164504-164504 (2013-11-05)
The dielectric relaxation of two long-chain glass forming monohydroxy alcohols, 2-butyl-1-octanol and 2-hexyl-1-decanol, is studied at low temperature. Remarkable broadening from the pure Debye relaxation is identified for the slowest dynamics, differing from the dielectric spectra of short-chain alcohols. The
View All Related Papers

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