Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

870710P

Avanti

10:0 Coenzyme A

Avanti Research™ - A Croda Brand 870710P, powder

Synonym(s):

decanoyl Coenzyme A (ammonium salt)

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C31H63N10O17P3S
CAS Number:
799812-83-2
Molecular Weight:
972.88
UNSPSC Code:
12352211
NACRES:
NA.25

form

powder

packaging

pkg of 1 × 10 mg (870710P-10mg)
pkg of 1 × 5 mg (870710P-5mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand 870710P

application(s)

lipidomics

lipid type

coenzymes

shipped in

dry ice

storage temp.

−20°C

SMILES string

O[C@@](C(NCCC(NCCSC(CCCCCCCCC)=O)=O)=O)(C(C)(COP([O-])(OP([O-])(OC[C@H]([C@H]1OP([O-])(O)=O)O[C@H]([C@@H]1O)N2C3=C(C(N)=NC=N3)N=C2)=O)=O)C)[H].[NH4+].[NH4+].[NH4+]

InChI

1S/C31H54N7O17P3S.3H3N/c1-4-5-6-7-8-9-10-11-22(40)59-15-14-33-21(39)12-13-34-29(43)26(42)31(2,3)17-52-58(49,50)55-57(47,48)51-16-20-25(54-56(44,45)46)24(41)30(53-20)38-19-37-23-27(32)35-18-36-28(23)38;;;/h18-20,24-26,30,41-42H,4-17H2,1-3H3,(H,33,39)(H,34,43)(H,47,48)(H,49,50)(H2,32,35,36)(H2,44,45,46);3*1H3/t20-,24?,25+,26+,30-;;;/m1.../s1

InChI key

IWPPTKRPCYMCQM-HGTZWQFESA-N

General description

10:0 Coenzyme A, also known as decanoyl Coenzyme A, is a coenzyme A derivative of decanoic acid. It is a medium-chain acyl CoA and is an intermediate of fatty acid metabolism. Decanoyl-CoA acts as a CqsA (acyl-CoA transferase) substrate for the synthesis of 3-aminotridecan-4-one (amino-CAI-1).

Application

Decanoyl Coenzyme A has been used as an internal standard to measure the decanoyl-CoA in the standard mixture analyzed with reversed phase ultrahigh performance liquid chromatography (UHPLC).

Packaging

5 mL Amber Glass Screw Cap Vial (870710P-10mg)
5 mL Amber Glass Screw Cap Vial (870710P-5mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

11 - Combustible Solids

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

László Abrankó et al.
Journal of chromatography. A, 1534, 111-122 (2018-01-02)
Fatty acyl-Coenzyme A species (acyl-CoAs) are key biomarkers in studies focusing on cellular energy metabolism. Existing analytical approaches are unable to simultaneously detect the full range of short-, medium-, and long-chain acyl-CoAs, while chromatographic limitations encountered in the analysis of
Robert C Kelly et al.
Nature chemical biology, 5(12), 891-895 (2009-10-20)
Vibrio cholerae, the bacterium that causes the disease cholera, controls virulence factor production and biofilm development in response to two extracellular quorum-sensing molecules, called autoinducers. The strongest autoinducer, called CAI-1 (for cholera autoinducer-1), was previously identified as (S)-3-hydroxytridecan-4-one. Biosynthesis of
Jake M Stout et al.
The Plant journal : for cell and molecular biology, 71(3), 353-365 (2012-02-23)
The psychoactive and analgesic cannabinoids (e.g. Δ(9) -tetrahydrocannabinol (THC)) in Cannabis sativa are formed from the short-chain fatty acyl-coenzyme A (CoA) precursor hexanoyl-CoA. Cannabinoids are synthesized in glandular trichomes present mainly on female flowers. We quantified hexanoyl-CoA using LC-MS/MS and

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service