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Merck

C1875

Decanoic acid

≥98.0%

Synonym(s):

1-Nonanecarboxylic acid, Acid C10, C10:0, Capric acid, NSC 5025

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About This Item

Linear Formula:
CH3(CH2)8COOH
CAS Number:
Molecular Weight:
172.26
UNSPSC Code:
12352211
NACRES:
NA.25
PubChem Substance ID:
EC Number:
206-376-4
Beilstein/REAXYS Number:
1754556
MDL number:

Product Name

Decanoic acid, ≥98.0%

InChI key

GHVNFZFCNZKVNT-UHFFFAOYSA-N

InChI

1S/C10H20O2/c1-2-3-4-5-6-7-8-9-10(11)12/h2-9H2,1H3,(H,11,12)

SMILES string

CCCCCCCCCC(O)=O

biological source

plant

vapor pressure

15 mmHg ( 160 °C)

assay

≥98.0%

form

crystals

bp

268-270 °C (lit.)

mp

27-32 °C (lit.)

density

0.893 g/mL at 25 °C (lit.)

functional group

carboxylic acid

lipid type

saturated FAs

shipped in

ambient

storage temp.

room temp

Quality Level

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Application

Decanoic acid is used in the preparation of ammonium decanoate (a surfactant) and for the preparation of disperse phase.

Biochem/physiol Actions

Decanoic acid is helpful in the attenuation of oxidative stress. Decanoic acid in ketogenic diet is involved in mitochondrial biogenesis thereby enhancing the citrate synthase and complex I activity of electron transport chain.

General description

Decanoic acid is a ten-carbon, saturated fatty acid. It is present in palm kernel, coconut fat and in milk fat.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

296.6 °F - closed cup

flash_point_c

147 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Function of capric acid in cyclophosphamide-induced intestinal inflammation, oxidative stress, and barrier function in pigs
Lee SI and Kang KS
Scientific reports, 7(1), 16530-16530 (2017)
Colloidal processing of macroporous TiO2 materials for photocatalytic water treatment
Natoli A, et al.
Journal of the American Ceramic Society. American Ceramic Society, 95(2), 502-508 (2012)
Lexicon of lipid nutrition (IUPAC Technical Report)
Beare-Rogers JL, et al.
Pure and Applied Chemistry. Chimie Pure Et Appliquee, 73(4), 685-744 (2001)
Principles of Orthomolecularism (2004)
A descriptive force-balance model for droplet formation at microfluidic Y-junctions
Steegmans MLJ, et al.
AIChE Journal, 56(10), 2641-2649 (2010)

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