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Merck
CN

870852C

Avanti

C18:1(Δ9-cis) Carnitine

Avanti Research™ - A Croda Brand

别名:

oleoyl L-carnitine

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关于此项目

经验公式（希尔记法）:
C25H47NO4
化学文摘社编号:
13962-05-5
分子量:
425.64
UNSPSC Code:
12352211
NACRES:
NA.25

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产品名称

C18:1(Δ9-cis) Carnitine, Avanti Research™ - A Croda Brand 870852C

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

assay

>99% (TLC)

form

liquid

packaging

pkg of 1 × 1 mL (870852C-5mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand 870852C

concentration

5 mg/mL (870852C-5mg)

lipid type

bioactive lipids

shipped in

dry ice

storage temp.

−20°C

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Application

C18:1(Δ9-cis) Carnitine may be used as an internal standard in tandem mass spectrometry (MS/MS) for quantitative measurement of carnitines in plasma sample.

Biochem/physiol Actions

C18:1(Δ9-cis) Carnitine, also known as oleoyl L-carnitine, has a potential to inhibit glycine transporter 2 (GLYT2) in a non-competitive manner. It is used as an effective therapeutic for treating pain.

Packaging

5 mL Clear Glass Sealed Ampule (870852C-5mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 - STOT SE 3

target_organs

Central nervous system, Liver,Kidney

存储类别

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

wgk

WGK 3

flash_point_f

does not flash

flash_point_c

does not flash

法规信息

危险化学品
易制毒化学品（2类）
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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

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