Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

485616

Sigma-Aldrich

Dodecylphosphorylcholine-d38

98 atom % D

Synonym(s):

Dodecylphosphocholine-d38

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
[CD3(CD2)11O](O-)P(=O)OCD2CD2N+(CD3)3
CAS Number:
130890-78-7
Molecular Weight:
389.70
MDL number:
MFCD01321393
UNSPSC Code:
12352211
PubChem Substance ID:
24872104
NACRES:
NA.12

isotopic purity

98 atom % D

Quality Level

200

form

solid

technique(s)

NMR: suitable
bio NMR: suitable

mp

247-249 °C (lit.)

mass shift

M+38

SMILES string

[O-]P(OC([2H])(C([N+](C([2H])([2H])[2H])(C([2H])([2H])[2H])C([2H])([2H])[2H])([2H])[2H])[2H])(OC([2H])(C([2H])(C([2H])(C([2H])(C([2H])(C([2H])(C([2H])(C([2H])(C([2H])(C([2H])(C([2H])(C([2H])([2H])[2H])[2H])[2H])[2H])[2H])[2H])[2H])[2H])[2H])[2H])[2H])[2H]

InChI

1S/C17H38NO4P/c1-5-6-7-8-9-10-11-12-13-14-16-21-23(19,20)22-17-15-18(2,3)4/h5-17H2,1-4H3/i1D3,2D3,3D3,4D3,5D2,6D2,7D2,8D2,9D2,10D2,11D2,12D2,13D2,14D2,15D2,16D2,17D2

InChI key

QBHFVMDLPTZDOI-DHIOKLJKSA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Niels Geudens et al.
Molecules (Basel, Switzerland), 24(12) (2019-06-20)
Cyclic lipodepsipeptides or CLiPs from Pseudomonas are secondary metabolites that mediate a wide range of biological functions for their producers, and display antimicrobial and anticancer activities. Direct interaction of CLiPs with the cellular membranes is presumed to be essential in
Ruslan Garifullin et al.
European biophysics journal : EBJ, 48(1), 25-34 (2018-08-15)
Chemical modification of therapeutic peptides is an important approach to improving their physicochemical and pharmacokinetic properties. The triphenylphosphonium (TPP) cation has proved to be a powerful modifier; however, its effects on peptide structure and activity remain uncharacterized. In this study
Nelson A Araujo et al.
Archives of biochemistry and biophysics, 698, 108731-108731 (2020-12-29)
Microbial pathogens, such as Trypanosoma brucei, have an enormous impact on global health and economic systems. Protein kinase A of T. brucei is an attractive drug target as it is an essential enzyme which differs significantly from its human homolog.
Ting-Wei Chang et al.
PloS one, 12(10), e0186442-e0186442 (2017-10-19)
Antimicrobial peptides are important components of the host innate defense mechanism against invading pathogens, especially for drug-resistant bacteria. In addition to bactericidal activity, the 25 residue peptide TP4 isolated from Nile tilapia also stimulates cell proliferation and regulates the innate
Soraya Serrano et al.
Biochemistry, 56(41), 5503-5511 (2017-09-21)
Despite extensive characterization of the human immunodeficiency virus type 1 (HIV-1) hydrophobic fusion peptide (FP), the structure-function relationships underlying its extraordinary degree of conservation remain poorly understood. Specifically, the fact that the tandem repeat of the FLGFLG tripeptide is absolutely

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service