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Sigma-Aldrich

Erucic acid

technical, ~90% (GC)

Synonym(s):

cis-13-Docosenoic acid, Prifac 2990

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About This Item

Linear Formula:
CH3(CH2)7CH=CH(CH2)11COOH
CAS Number:
112-86-7
Molecular Weight:
338.57
Beilstein:
1728049
EC Number:
204-011-3
MDL number:
MFCD00063188
UNSPSC Code:
12352100
PubChem Substance ID:
57650471
NACRES:
NA.22

grade

technical

Assay

~90% (GC)

form

powder or crystals

bp

358 °C/400 mmHg (lit.)

mp

28-32 °C (lit.)

functional group

carboxylic acid

SMILES string

[H]\C(CCCCCCCC)=C(/[H])CCCCCCCCCCCC(O)=O

InChI

1S/C22H42O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22(23)24/h9-10H,2-8,11-21H2,1H3,(H,23,24)/b10-9-

InChI key

DPUOLQHDNGRHBS-KTKRTIGZSA-N

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Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315 - H319 - H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

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

Certificates of Analysis (COA)

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W B Rizzo et al.
Neurology, 39(11), 1415-1422 (1989-11-01)
We investigated the biochemical and clinical efficacy of dietary erucic acid (C22:1) therapy for X-linked adrenoleukodystrophy (ALD). In a double-blind crossover study of patients who were on chronic oleic acid (C18:1) therapy, addition of erucic acid to the diet led
Processing of crambe for oil and isolation of erucic acid.
Vargas-Lopez JM, et al.
Journal of the American Oil Chemists' Society, 76(7), 801-809 (1999)
Bifang Cheng et al.
Transgenic research, 19(2), 221-229 (2009-07-08)
Eicosapentaenoic acid (EPA, 20:5n-3) plays an important role in many aspects of human health. In our efforts towards producing high levels of EPA in plants, we investigated the effects of different host species, genes and promoters on EPA biosynthesis. Zero-erucic
Shiva Shanker Kaki et al.
Biotechnology and bioengineering, 110(1), 78-86 (2012-07-20)
The enzymatic conversion of mixtures of multiple substrates was studied quantitatively, based on established methodology used for the enzymatic kinetic resolution of racemic mixtures, involving the use of competitive factors: ratios of specificity constants (k(cat)/K(M)) of substrate pairs. The competitive
Gang Wu et al.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 116(4), 491-499 (2007-12-14)
The fatty acid elongase 1 (FAE1) gene is a key gene in the erucic acid biosynthesis in rapeseed. The complete coding sequences of the FAE1 gene were isolated separately from eight high and zero erucic acid rapeseed cultivars (Brassica napus
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