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45630

Sigma-Aldrich

Erucic acid

technical, ~90% (GC)

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Synonym(s):
cis-13-Docosenoic acid, Prifac 2990
Linear Formula:
CH3(CH2)7CH=CH(CH2)11COOH
CAS Number:
Molecular Weight:
338.57
Beilstein/REAXYS Number:
1728049
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

grade

technical

Quality Level

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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This Item
E3385586064364525
Erucic acid technical, ~90% (GC)

45630

Erucic acid

Erucic acid ≥99% (capillary GC)

E3385

Erucic acid

Behenic-d43 acid 98 atom % D, 98% (CP)

586064

Behenic-d43 acid

Oleic acid technical grade, 90%

364525

Oleic acid

functional group

carboxylic acid

functional group

carboxylic acid

functional group

-

functional group

oleic acid

grade

technical

grade

-

grade

-

grade

-

form

powder or crystals

form

powder

form

solid

form

liquid, semisolid, waxy solid

mp

28-32 °C (lit.)

mp

28-32 °C (lit.)

mp

80-82 °C

mp

13-14 °C (lit.)

bp

358 °C/400 mmHg (lit.)

bp

358 °C/400 mmHg (lit.)

bp

306 °C

bp

194-195 °C/1.2 mmHg (lit.)

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


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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)
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
Florian Stempfle et al.
Macromolecular rapid communications, 34(1), 47-50 (2012-11-20)
Self-metathesis of erucic acid by [(PCy(3))(η-C-C(3)H(4)N(2)Mes(2))Cl(2)Ru = CHPh] (Grubbs second- generation catalyst) followed by catalytic hydrogenation and purification via the ester yields 1,26-hexacosanedioate (>99% purity). Polyesterification with 1,26-hexacosanediol, generated from the diester, affords polyester-26,26, which features a T(m) of 114
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

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