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711047

Sigma-Aldrich

1,2-Dimyristoyl-d54-sn-glycero-3-phosphocholine

98 atom % D, 97% (CP)

Synonym(s):

1,2-Ditetradecanoyl-d54-sn-glycero-3-phosphocholine, 3-sn-Phosphatidylcholine,1,2-dimyristoyl-d54

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About This Item

Empirical Formula (Hill Notation):
C36D54H18NO8P
Molecular Weight:
732.27
MDL number:
UNSPSC Code:
12352108
PubChem Substance ID:

isotopic purity

98 atom % D

assay

97% (CP)

form

solid

mol wt

731.18 by atom % calculation

mass shift

M+54

storage temp.

−20°C

SMILES string

[O-]P(OCC[N+](C)(C)C)(OC[C@]([H])(OC(C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])[2H])=O)COC(C([2H])([2H])C([2H])([2H])C([2H])([2H

InChI

1S/C36H72NO8P/c1-6-8-10-12-14-16-18-20-22-24-26-28-35(38)42-32-34(33-44-46(40,41)43-31-30-37(3,4)5)45-36(39)29-27-25-23-21-19-17-15-13-11-9-7-2/h34H,6-33H2,1-5H3/t34-/m1/s1/i1D3,2D3,6D2,7D2,8D2,9D2,10D2,11D2,12D2,13D2,14D2,15D2,16D2,17D2,18D2,19D2,20D2,21D2,22D2,23D2,24D2,25D2,26D2,27D2,28D2,29D2

InChI key

CITHEXJVPOWHKC-RPLUSTTMSA-N

Packaging

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

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Miranda L Schmidt et al.
Biochimica et biophysica acta, 1858(4), 619-626 (2015-12-27)
Magnetically orienting bicelles are often made by combining the long chain phospholipid 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) with the short chain phospholipid 1,2-dicaproyl-sn-glycero-3-phosphocholine (DCPC) in buffer. These bicelles orient with their bilayer normals perpendicular to the external magnetic field. We have examined the
Katarzyna Trzeciak et al.
Biochimica et biophysica acta. Biomembranes, 1862(2), 183066-183066 (2019-10-22)
In this work the conformation of dermorphin, Tyr-D-Ala-Phe-Gly-Tyr-Pro-Ser-NH2, an opioid peptide and its analogues with different stereochemistry of alanine and different C-terminus is studied in aqueous and membrane environments. Using two-dimensional NMR techniques we demonstrate that in D2O/H2O peptides with
Justine Wolf et al.
Biophysical journal, 113(6), 1290-1300 (2017-07-25)
The histidine-rich designer peptide LAH4-L1 exhibits antimicrobial and potent cell-penetrating activities for a wide variety of cargo including nucleic acids, polypeptides, adeno-associated viruses, and nanodots. The non-covalent complexes formed between the peptide and cargo enter the cell via an endosomal
Gary Bryant et al.
Colloids and surfaces. B, Biointerfaces, 177, 196-203 (2019-02-12)
Deuteration of phospholipids is a common practice to elucidate membrane structure, dynamics and function, by providing selective visualisation in neutron scattering, nuclear magnetic resonance and vibrational spectroscopy. It is generally assumed that the properties of the deuterated lipids are identical
Johannes Franz et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(40), 9690-9697 (2017-05-16)
Nitrated fatty acids (NO

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