An internal standard for the quantification of 1,2-dipalmitoyl-sn-glycero-3-PG
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1-Palmitoyl-d9-2-Palmitoyl-sn-glycero-3-PG

Item No. 28953

Technical Information
Formal Name
(2R)-3-((((R)-2,3-dihydroxypropoxy)(hydroxy)phosphoryl)oxy)-2-(palmitoyloxy)propyl hexadecanoate-13,13,14,14,15,15,16,16,16-d9
Synonyms
  • 1-Hexanoyl-d9-2-hexanoyl-sn-glycero-3-phosphatidylglycerol
  • 1-Hexanoyl-d9-2-hexanoyl-sn-glycero-3-phosphoglycerol
  • 1-Palmitoyl-d9-2-Palmitoyl-sn-glycero-3-phosphatidylglycerol
  • 1-Palmitoyl-d9-2-Palmitoyl-sn-glycero-3-phosphoglycerol
  • 16:0-d9/16:0-PG
  • PG(16:0-d9/16:0)
Molecular Formula
C38H66D9O10P
Formula Weight
Purity
≥99% deuterated forms (d1-d9)
Formulation
A 1 mg/ml solution in chloroform
Chloroform: 1 mg/ml
SMILES
O=C(CCCCCCCCCCCC([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])[2H])OC[C@@H](OC(CCCCCCCCCCCCCCC)=O)COP(OCC(O)CO)(O)=O
InChi Code
InChI=1S/C38H75O10P/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-37(41)45-33-36(34-47-49(43,44)46-32-35(40)31-39)48-38(42)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h35-36,39-40H,3-34H2,1-2H3,(H,43,44)/t35?,36-/m1/s1/i1D3,3D2,5D2,7D2
InChi Key
BIABMEZBCHDPBV-RUEHLNHXSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Product Description

    1-Palmitoyl-d9-2-palmitoyl-sn-glycero-3-PG is intended for use as an internal standard for the quantification of 1,2-dipalmitoyl-sn-glycero-3-PG (1,2-DPPG; Item No. 15086) by GC- or LC-MS. 1,2-DPPG is a phospholipid containing the long-chain (16:0) palmitic acid inserted at the sn-1 and sn-2 positions. It can be used in the generation of micelles, liposomes, and other types of artificial membranes.1,2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Ege, C., and Lee, K.Y.C. Insertion of Alzheimer’s Aβ40 peptide into lipid monolayers. Biophys. J. 87(3), 1732-1740 (2004).

    2. Mansour, H.M., and Zografi, G. The relationship between water vapor absorption and desorption by phospholipids and bilayer phase transitions. J. Pharm. Sci. 96(2), 377-396 (2007).