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Merck

H6883

3-(N,N-Dimethylpalmitylammonio)propanesulfonate

≥98% (TLC)

Synonyme(s) :

3-(N,N-Dimethylhexadecylammonio)propanesulfonate, 3-(Hexadecyldimethylammonio)propanesulfonate, 3-(Palmityldimethylammonio)propanesulfonate, Palmityl sulfobetaine, SB3-16

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A propos de cet article

Formule linéaire :
CH3(CH2)15N+(CH3)2CH2CH2CH2SO3-
Numéro CAS:
2281-11-0
Poids moléculaire :
391.65
UNSPSC Code:
12161900
NACRES:
NA.25
PubChem Substance ID:
24895773
EC Number:
218-918-7
Beilstein/REAXYS Number:
4149854
MDL number:
MFCD00036911

Principaux documents

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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

SMILES string

CCCCCCCCCCCCCCCC[N+](C)(C)CCCS([O-])(=O)=O

description

zwitterionic

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

Quality Level

200

Catégories apparentées

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.

Classe de stockage

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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Certificats d'analyse (COA)

Lot/Batch Number
0000505425
0000535062
0000505425
0000535062
0000516123

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Consulter la Bibliothèque de documents

R J Barry et al.
The Journal of biological chemistry, 264(16), 9231-9238 (1989-06-05)
Studies reported previously from this laboratory have demonstrated that membranes from the pigment epithelium of the vertebrate eye can transform free all-trans-retinol to 11-cis-retinol as well as 11-cis- and all trans-retinyl esters (Bernstein, P. S., Law, W. C., and Rando
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
M Lui et al.
Analytical biochemistry, 241(2), 156-166 (1996-10-15)
We have analyzed the efficacies of seven different organic solvents, 13 organic bases, and 17 detergents to dissociate electroblotted proteins from nitrocellulose. Most efficient were a 1% piperidine-40% acetonitrile mixture and 1% concentrations of either cetyltrimethylammonium bromide or several polyoxyethylene
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