700018P
Avanti
24(R/S)-hydroxycholesterol-d7
Avanti Research™ - A Croda Brand
Synonym(s):
25,26,26,26,27,27,27-heptadeuterocholest-5-ene-3β,24-diol
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All Photos(2)
About This Item
Empirical Formula (Hill Notation):
C27H39D7O2
CAS Number:
Molecular Weight:
409.70
UNSPSC Code:
12352100
NACRES:
NA.25
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description
cholest-5-ene-3β,24(R/S)-diol-d7
Assay
>99% (TLC)
form
powder
packaging
pkg of 1 × 1 mg (700018P-1mg)
pkg of 1 × 5 mg (700018P-5mg)
manufacturer/tradename
Avanti Research™ - A Croda Brand
shipped in
dry ice
storage temp.
−20°C
General description
24(R/S)-hydroxycholesterol-d7 is the deuterated form of 24(R/S)-hydroxycholesterol.
Application
24(R/S)-hydroxycholesterol-d7 has been used as an internal standard in the quantification of sterols from biological samples by gas chromatography-mass spectrometry (GC–MS). It has also been used as an internal standard for the quantification of monohydroxycholesterols by MS analysis.
Packaging
5 mL Amber Glass Screw Cap Vial (700018P-1mg)
5 mL Amber Glass Screw Cap Vial (700018P-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’.
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William J Griffiths et al.
Free radical biology & medicine, 59, 69-84 (2012-08-01)
Bile acids, bile alcohols, and hormonal steroids represent the ultimate biologically active products of cholesterol metabolism in vertebrates. However, intermediates in their formation, including oxysterols and cholestenoic acids, also possess known, e.g., as ligands to nuclear and G-protein-coupled receptors, and
Andrea Civra et al.
The Journal of steroid biochemistry and molecular biology, 193, 105424-105424 (2019-07-16)
Oxysterols are cholesterol oxidation derivatives. Those containing an additional hydroxyl group on the side chain of the cholesterol molecule result from a physiological enzymatic synthesis and include the majority of oxysterols present in the circulation. Among these, 25-hydroxycholesterol (25OHC) and
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