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A3631

Sigma-Aldrich

Arachidic acid

≥99%

Synonym(s):

Arachic acid, Arachidinic acid, Eicosanoic acid, Icosanoic acid, NSC 93983

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About This Item

Linear Formula:
CH3(CH2)18COOH
CAS Number:
Molecular Weight:
312.53
Beilstein:
1788211
EC Number:
MDL number:
UNSPSC Code:
12352211
PubChem Substance ID:
NACRES:
NA.25

Assay

≥99%

form

crystalline powder

technique(s)

HPLC: suitable

mp

74-76 °C (lit.)

functional group

carboxylic acid

lipid type

omega FAs

shipped in

ambient

storage temp.

−20°C

SMILES string

CCCCCCCCCCCCCCCCCCCC(O)=O

InChI

1S/C20H40O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22/h2-19H2,1H3,(H,21,22)

InChI key

VKOBVWXKNCXXDE-UHFFFAOYSA-N

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Application

Arachidic acid has been used as a fatty acid standard to optimize a sensitive high-performauce liquid chromatography (HPLC) method to analyse fatty acid (FA) for the quantification of polyunsaturated FAs (PUFAs) in cell lipid extracts.

Biochem/physiol Actions

Arachidic acid is a saturated fatty acid with a 20 carbon chain. Arachidic acid occurs naturally in fish and vegetable oils. Diets rich in saturated fats like arachidic acid are associated with increased levels of serum low density lipoproteins.

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

nwg

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °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’.

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Lipids in blood-brain barrier models in vitro I: thin-layer chromatography and high-performance liquid chromatography for the analysis of lipid classes and long-chain polyunsaturated fatty acids
Kraamer SD, et al.
In Vitro Cellular & Developmental Biology. Animal, 38(10), 557-565 (2002)
ATTY ACIDS| Properties
Encyclopedia of food sciences and nutrition (2003)
Archan Dey et al.
Nature materials, 9(12), 1010-1014 (2010-11-16)
Unravelling the processes of calcium phosphate formation is important in our understanding of both bone and tooth formation, and also of pathological mineralization, for example in cardiovascular disease. Serum is a metastable solution from which calcium phosphate precipitates in the
Caiyan Lu et al.
Analytical chemistry, 83(1), 351-358 (2010-12-03)
An organic delta layer system made of alternating Langmuir-Blodgett multilayers of barium arachidate (AA) and barium dimyristoyl phosphatidate (DMPA) was constructed to elucidate the factors that control depth resolution in molecular depth profile experiments. More specifically, one or several bilayers
Ubonvan Termsarasab et al.
Colloids and surfaces. B, Biointerfaces, 109, 280-286 (2013-05-15)
Arachidyl chitosan (chitosan oligosaccharide-arachidic acid; CSOAA)-based self-assembled nanoprobes for magnetic resonance imaging (MRI) of neoplastic lesions was developed and evaluated in vitro. Diethylenetriaminepentaacetic dianhydride (DTPA) was conjugated to chitosan oligosaccharide (CSO) and Gd(3+) was chelated to the resulting ligand. DTPA

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