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810206P

Avanti

NBD Sphinganine

omega(7-nitro-2-1,3-benzoxadiazol-4-yl)(2S,3R)-2-aminooctadecane-1,3-diol, powder

Synonym(s):

D-erythro-sphinganine-N-NBD; NBD-dihydrosphingosine

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About This Item

Empirical Formula (Hill Notation):
C24H41N5O5
CAS Number:
Molecular Weight:
479.61
UNSPSC Code:
12352211
NACRES:
NA.25

Assay

>99% (TLC)

form

powder

packaging

pkg of 1 × 100 μg ((810206P-100UG))
pkg of 1 × 250 μg (810206P-250ug)
pkg of 1 × 50 μg (810206P-50UG)

manufacturer/tradename

Avanti Research - A Croda Brand 810206P

shipped in

dry ice

storage temp.

−20°C

General description

Sphinganine, also called as dihydrosphingosine is a common sphingoid base in phospholipids.

Application

NBD Sphinganine or omega (7-nitro-2-1,3-benzoxadiazol-4-yl)(2S,3R)-2-aminooctadecane-1,3-diol is suitable for the analysis of the dihydrosphingosine (DHS) localization to endoplasmic reticulum for the activation of activating transcription factor 6 (ATF6) protein.
NBD Sphinganine or omega(7-nitro-2-1,3-benzoxadiazol-4-yl)(2S,3R)-2-aminooctadecane-1,3-diol is suitable for the analysis of the dihydrosphingosine (DHS) localization to endoplasmic reticulum for the activation of activating transcription factor 6 (ATF6) protein.

Packaging

5 mL Amber Glass Screw Cap Vial (810206P-100UG)
5 mL Amber Glass Screw Cap Vial (810206P-250UG)
5ML Glass Amber Screw Cap Vial (810206P-50UG)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

No data available

Flash Point(C)

No data available


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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Junliang Wan et al.
Journal of agricultural and food chemistry, 67(46), 12953-12961 (2019-10-23)
Most common sphingolipids are comprised of "typical" sphingoid bases (sphinganine, sphingosine, and structurally related compounds) and are produced via the condensation of l-serine with a fatty acyl-CoA by serine palmitoyltransferase. Some organisms, including mammals, also produce "atypical" sphingoid bases that

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