An internal standard for the quantification of 1,2-dipalmitoyl-rac-glycero-3-PC
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1,2-Dipalmitoyl-d6-rac-glycero-3-PC

Item No. 28932

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
4-hydroxy-N,N,N-trimethyl-10-oxo-7-[(1-oxohexadecyl-16,16,16-d3)oxy]-3,5,9-trioxa-4-phosphapentacosan-25,25,25-d3-1-aminium, inner salt, 4-oxide
CAS Number
82765-17-1
Synonyms
  • 16:0/16:0-d6-PC
  • PC(16:0/16:0)-d6
  • 1,2-Dihexadecanoyl-d6-rac-glycero-3-Phosphocholine
  • 1,2-Dihexadecanoyl-d6-rac-glycero-3-Phosphatidylcholine
Molecular Formula
C40H74D6NO8P
Formula Weight
740.1
Purity
≥99% deuterated forms (d1-d6)
Formulation
A solid
Solubility(Learn about Variance in Solubility)
Methanol: Soluble
SMILES
O=C(CCCCCCCCCCCCCCC([2H])([2H])[2H])OCC(OC(CCCCCCCCCCCCCCC([2H])([2H])[2H])=O)COP(OCC[N+](C)(C)C)([O-])=O
InChi Code
InChI=1S/C40H80NO8P/c1-6-8-10-12-14-16-18-20-22-24-26-28-30-32-39(42)46-36-38(37-48-50(44,45)47-35-34-41(3,4)5)49-40(43)33-31-29-27-25-23-21-19-17-15-13-11-9-7-2/h38H,6-37H2,1-5H3/i1D3,2D3
InChi Key
KILNVBDSWZSGLL-WFGJKAKNSA-N
Side Chain Carbon Sum
32:0
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    1,2-Dipalmitoyl-d6-rac-glycero-3-PC is intended for use as an internal standard for the quantification of 1,2-dipalmitoyl-rac-glycero-3-PC by GC- or LC-MS. 1,2-Dipalmitoyl-rac-glycero-3-PC is a phospholipid that contains palmitic acid (Item No. 10006627) at the sn-1 and sn-2 positions. It has been used as a component of liposomes, monolayers, and bilayers to study the influence of chirality on membrane dynamics.1,2,3,4 1,2-dipalmitoyl-rac-glycero-3-PC has been used to study electric field-induced orientation of phospholipid head groups and dynamics of liposomal phase transitions.2,3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Vollhardt, D., Nandi, N., and Banki, S.D. Nanoaggregate shapes at the air/water interface. Phys. Chem. Chem. Phys. 13(11), 4812-4829 (2011).

    2. Mishima, K., Tanaka, S., and Ogihara, T. Electric field-induced orientation of L- and DL-phosphatidylcholine bilayers. Biochim. Biophys. Acta 1565(1), 107-111 (2002).

    3. Boyanov, A.I., Tenchov, B.G., Koynova, R.D., et al. Absence of subtransition in racemic dipalmitoylphosphatidylcholine vesicles. Biochim. Biophys. Acta 732, 711-713 (1983).

    4. Moy, V.T., Keller, D.J., Gaub, H.E., et al. Long-range molecular orientational order in monolayer solid domains of phospholipid. J. Phys. Chem. 90(14), 3198-3202 (1986).