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About This Item
Linear Formula:
CH3(CH2)15N+(CH3)2CH2CH2CH2SO3-
CAS Number:
Molecular Weight:
391.65
UNSPSC Code:
12161900
NACRES:
NA.25
PubChem Substance ID:
EC Number:
218-918-7
Beilstein/REAXYS Number:
4149854
MDL number:
description
zwitterionic
Quality Level
assay
≥98% (TLC)
mol wt
micellar avg mol wt 60,700
aggregation number
155
technique(s)
electrophoresis: suitable, mass spectrometry (MS): suitable, thin layer chromatography (TLC): suitable
conductivity
≤10 μmho per cm at 24 °C (0.05 M aqueous solution)
CMC
0.01-0.06 mM (20-25°C)
application(s)
cell analysis
SMILES string
CCCCCCCCCCCCCCCC[N+](C)(C)CCCS([O-])(=O)=O
InChI
1S/C21H45NO3S/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-19-22(2,3)20-18-21-26(23,24)25/h4-21H2,1-3H3
InChI key
TUBRCQBRKJXJEA-UHFFFAOYSA-N
General description
3-(N,N-Dimethylpalmitylammonio)propanesulfonate is a zwitterionic detergent.
Application
3-(N,N-Dimethylpalmitylammonio)propanesulfonate has been used in a study to assess the characterization of rat dihydroceramide desaturase. It has also been used in a study to investigate the inhibition of mitochondrial carnitine–acylcarnitine translocase by sulfobetaines. It is also used for extraction of proteins for analysis by chromatography, mass spectroscopy, and electrophoretic methods.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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R Parvin et al.
Canadian journal of biochemistry, 58(10), 822-830 (1980-10-01)
Sulfobetaines (N-alkyl-N,N-dimethyl-3-ammonio-1-propanesulfonates) have been identified as relatively specific and selective inhibitors of mitochondrial carnitine-acylcarnitine translocase. Thus, sublytic concentrations of sulfobetaines (alkyl = octyl to tetradecyl) inhibit the respiration of rat heart mitochondria supported by added acylcarnitines or pyruvate plus malonate
C Causeret et al.
Lipids, 35(10), 1117-1125 (2000-12-05)
The introduction of the double bond in the sphingoid backbone of sphingolipids occurs at the level of dihydroceramide via an NADPH-dependent desaturase, as discovered in permeabilized rat hepatocytes. In the rat, the enzyme activity, which has now been further characterized
H Erdjument-Bromage et al.
Journal of chromatography. A, 826(2), 167-181 (1999-01-01)
Mass spectrometry occupies a central position in most current protein identification schemes. So-called 'mass fingerprinting' techniques rely on composite mass patterns of proteolytic fragments, or dissociation products thereof, to query databases. Keys to successful analysis of ever smaller amounts are
Global Trade Item Number
| SKU | GTIN |
|---|---|
| H6883-25G | 04061833802397 |
| H6883-5G | 04061833611463 |