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Merck
CN

860625P

Avanti

C2 Dihydroceramide (d18:0/2:0)

Avanti Research - A Croda Brand

别名:

N-acetoyl-D-erythro-sphinganine

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关于此项目

经验公式(希尔记法):
C20H41NO3
化学文摘社编号:
分子量:
343.54
MDL number:
UNSPSC Code:
12352211
NACRES:
NA.25
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产品名称

C2 Dihydroceramide (d18:0/2:0), Avanti Research - A Croda Brand 860625P, powder

assay

>99% (TLC)

form

powder

packaging

pkg of 1 × 5 mg (860625P-5mg)

manufacturer/tradename

Avanti Research - A Croda Brand 860625P

lipid type

sphingolipids

shipped in

dry ice

storage temp.

−20°C

SMILES string

OC[C@]([H])(NC(C)=O)[C@]([H])(O)CCCCCCCCCCCCCCC

InChI

1S/C20H41NO3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-20(24)19(17-22)21-18(2)23/h19-20,22,24H,3-17H2,1-2H3,(H,21,23)/t19-,20+/m0/s1

InChI key

CRJGESKKUOMBCT-VQTJNVASSA-N

General description

Dihydroceramide belongs to the ceramide family. It contains sphinganine, which is devoid of the 4,5-trans-double bond in the sphingoid base backbone.

Application

C2 Dihydroceramide (d18:0/2:0) has been used as a lipid standard in the analysis of sphingolipids by tandem mass spectrometry. It is also suitable for inducing stress in embryos to study stress-induced apoptosis in larval embryos of Japanese flounder.

Biochem/physiol Actions

Dihydroceramide is synthesized by the N-acylation of dihydrosphingosine. It functions as an inactive precursor for ceramide in de novo sphingolipid synthesis. (Dihydro)-ceramide desaturase catalyzes the conversion of dihydroceramide to ceramide by the addition of C4−5 trans-double bond in the sphingoid backbone. Dihydroceramide has an ability to induce autophagy.

Packaging

5 mL Amber Glass Screw Cap Vial (860625P-5mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC


存储类别

11 - Combustible Solids



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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