Skip to Content
Merck
All Photos(1)

Key Documents

870852P

Avanti

C18:1(Δ9-cis) Carnitine

Avanti Polar Lipids 870852P, powder

Synonym(s):

oleoyl L-carnitine

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C25H47NO4
CAS Number:
Molecular Weight:
425.64
UNSPSC Code:
12352211
NACRES:
NA.25

form

powder

packaging

pkg of 1 × 5 mg (870852P-5mg)

manufacturer/tradename

Avanti Polar Lipids 870852P

lipid type

bioactive lipids

shipped in

dry ice

storage temp.

−20°C

SMILES string

C[N+](C)(C)C[C@H](OC(CCCCCCC/C=C\CCCCCCCC)=O)CC([O-])=O

InChI

1S/C25H47NO4/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-25(29)30-23(21-24(27)28)22-26(2,3)4/h12-13,23H,5-11,14-22H2,1-4H3/b13-12-

InChI key

IPOLTUVFXFHAHI-SEYXRHQNSA-N

Application

C18:1(Δ9-cis) Carnitine may be used as an internal standard to measure the levels of carnitines in plasma samples by tandem mass spectrometry (MS/MS).

Biochem/physiol Actions

C18:1(Δ9-cis) Carnitine or oleoyl L-carnitine, is an endogenous acylcarnitine. It is a potential non-competitive inhibitor of glycine transporter 2 (GLYT2). Oleoyl L-carnitine is used as an effective therapeutic for treating pain.

Packaging

5 mL Clear Glass Sealed Ampule (870852P-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

J E Carland et al.
British journal of pharmacology, 168(4), 891-902 (2012-09-18)
Concentrations of extracellular glycine in the CNS are regulated by two Na(+)/Cl(-) -dependent glycine transporters, GlyT1 and GlyT2. Selective inhibitors of GlyT1 have been developed for the treatment of schizophrenia, whilst selective inhibitors of GlyT2 are analgesic in animal models

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