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464430

Sigma-Aldrich

2-Butyloctanoic acid

96%

Synonym(s):

α-Butylcaprylic acid, 2-Butyl-caprylic acid, 2-Butyloctanoic acid

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About This Item

Linear Formula:
CH3(CH2)5CH[(CH2)3CH3]CO2H
CAS Number:
Molecular Weight:
200.32
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

96%

refractive index

n20/D 1.438 (lit.)

bp

230 °C (lit.)

density

0.887 g/mL at 25 °C (lit.)

functional group

carboxylic acid

SMILES string

CCCCCCC(CCCC)C(O)=O

InChI

1S/C12H24O2/c1-3-5-7-8-10-11(12(13)14)9-6-4-2/h11H,3-10H2,1-2H3,(H,13,14)

InChI key

OARDBPIZDHVTCK-UHFFFAOYSA-N

General description

2-Butyloctanoic acid is a 2-butyl-substituted carboxylic acid.

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Overcrowding factors of mosquito larvae. VI. Structure-activity relations of 2-substituted aliphatic carboxylic acids against mosquito larvae.
Hwang Y-S, et al.
Journal of Agricultural and Food Chemistry, 22(6), 1004-1006 (1974)
Aki Maruoka et al.
Biocontrol science, 25(2), 63-71 (2020-06-09)
House dust mites, Dermatophagoides pteronyssinus are present in the indoor environments, such as pillows and carpets. In this study, we investigated the mite control effect of branched chain fatty acids (2-ethylhexanoic acid (iso-C8), 2-butyloctanoic acid (iso-C12), isopalmitic acid (iso-C16) and
Jumat Salimon et al.
Journal of automated methods & management in chemistry, 2011, 263624-263624 (2011-10-19)
A study was conveyed to produce estolide ester using ricinoleic acid as the backbone. The ricinoleic acid reacted with saturated fatty acid from C8-C18. These reactions were conducted under vacuum at 60°C for 24 h without solvent. The reaction used acid
Pishan Chang et al.
Neuropharmacology, 69, 105-114 (2012-11-28)
The medium chain triglyceride (MCT) ketogenic diet is used extensively for treating refractory childhood epilepsy. This diet increases the plasma levels of medium straight chain fatty acids. A role for these and related fatty acids in seizure control has not

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