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711047

Sigma-Aldrich

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

98 atom % D, 97% (CP)

Sinônimo(s):

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

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About This Item

Fórmula empírica (Notação de Hill):
C36D54H18NO8P
Peso molecular:
732.27
Número MDL:
Código UNSPSC:
12352108
ID de substância PubChem:

pureza isotópica

98 atom % D

Ensaio

97% (CP)

forma

solid

peso molecular

731.18 by atom % calculation

alteração de massa

M+54

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

[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

chave InChI

CITHEXJVPOWHKC-RPLUSTTMSA-N

Categorias relacionadas

Embalagem

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.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable


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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
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
Irène Nicolas et al.
PLoS biology, 17(7), e3000337-e3000337 (2019-07-10)
Antibiotics are a medical wonder, but an increasing frequency of resistance among most human pathogens is rendering them ineffective. If this trend continues, the consequences for public health and for the general community could be catastrophic. The current clinical pipeline

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