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860389P

Avanti

26:0-d4 Lyso PC

1-hexacosanoyl-d4-2-hydroxy-sn-glycero-3-phosphocholine, powder

Sinônimo(s):

1-hexacosanoyl(12,12,13,13-D4)-sn-glycero-3-phosphocholine

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About This Item

Fórmula empírica (Notação de Hill):
C34H66D4NO7P
Número CAS:
1246303-15-0
Peso molecular:
639.92
Número MDL:
MFCD22416868
Código UNSPSC:
12352100
NACRES:
NA.25

Ensaio

>99% (LPC; may contain up to 10% of the 2-LPC isomer, TLC)

Formulário

powder

embalagem

pkg of 1 × 1 mg (860389P-1mg)
pkg of 1 × 5 mg (860389P-5mg)

fabricante/nome comercial

Avanti Research™ - A Croda Brand 860389P

Condições de expedição

dry ice

temperatura de armazenamento

−20°C

Descrição geral

26:0-d4 Lyso PC is a deuterated lysophosphatidylcholine (lyso pc) in which 4 protons of hexacosanoyl are replaced by deuterium.

Aplicação

26:0-d4 Lyso PC has been used as an internal standard to extract total very long chain fatty acids (VLCFAs) from brain, testes and adrenal glands.

Embalagem

5 mL Amber Glass Screw Cap Vial (860389P-1mg)
5 mL Amber Glass Screw Cap Vial (860389P-5mg)

Informações legais

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Código de classe de armazenamento

11 - Combustible Solids

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Certificados de análise (COA)

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Walter C Hubbard et al.
Molecular genetics and metabolism, 97(3), 212-220 (2009-05-09)
Newborn screening for X-linked adrenoleukodystrophy (X-ALD) has until now been limited in implementation because of the lack of an accepted standard methodology. We have previously reported a technique using LC-MS/MS analysis that could provide the basis for screening of newborns
Wedad Fallatah et al.
Disease models & mechanisms, 13(1) (2019-12-22)
Rhizomelic chondrodysplasia punctata (RCDP) is a rare genetic disorder caused by mutations in peroxisomal genes essential for plasmalogen biosynthesis. Plasmalogens are a class of membrane glycerophospholipids containing a vinyl-ether-linked fatty alcohol at the sn-1 position that affect functions including vesicular
A thyroid hormone-based strategy for correcting the biochemical abnormality in X-linked adrenoleukodystrophy
Hartley MD, et al.
Endocrinology, 158(5), 1328-1338 (2017)
John Williams et al.
Bioanalysis, 12(3), 143-158 (2020-02-14)
Aim: Very long chain fatty acids (VLCFAs) have been identified as biomarkers for several peroxisomal disorders necessitating the need for reliable biomarker assays in particular C20, C22, C24, C26 in cerebrospinal fluid (CSF). Until now no absolute quantitation assay for

Global Trade Item Number

SKUGTIN
860389P-1MG4061835186532
860389P-5MG4061835186549

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