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H6883

Sigma-Aldrich

3-(N,N-Dimethylpalmitylammonio)propanesulfonate

≥98% (TLC)

Synonym(s):

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

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500 G
157,00 $

157,00 $


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500 G
157,00 $

About This Item

Linear Formula:
CH3(CH2)15N+(CH3)2CH2CH2CH2SO3-
CAS Number:
Molecular Weight:
391.65
Beilstein/REAXYS Number:
4149854
EC Number:
MDL number:
UNSPSC Code:
12161900
PubChem Substance ID:
NACRES:
NA.25

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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

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1 of 4

This Item
A72621.932171.01116
form

powder, solid

form

solid

form

solid

form

solid

assay

≥97%

assay

≥98%

assay

-

assay

≥98.0% (acidimetric)

Quality Level

200

Quality Level

200

Quality Level

-

Quality Level

300

grade

ACS reagent

grade

reagent grade

grade

ACS reagent

grade

ACS reagent

vapor pressure

<0.001 hPa

vapor pressure

-

vapor pressure

-

vapor pressure

-

mp

110-112 °C (dec.) (lit.)

mp

110-112 °C (dec.) (lit.)

mp

110-112 °C (dec.) (lit.)

mp

114 °C

General description

3-(N,N-Dimethylpalmitylammonio)propanesulfonate is a zwitterionic detergent. [1]

Application

3-(N,N-Dimethylpalmitylammonio)propanesulfonate has been used in a study to assess the characterization of rat dihydroceramide desaturase. [2] It has also been used in a study to investigate the inhibition of mitochondrial carnitine–acylcarnitine translocase by sulfobetaines. [3] It is also used for extraction of proteins for analysis by chromatography, mass spectroscopy, and electrophoretic methods.

Storage Class

11 - Combustible Solids

wgk_germany

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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Separation of the Positional Isomer Quinocide from the Anti-Malarial Drug Primaquine Using a Discovery? HS F5 HPLC Column.
Brondz I and Klein U.
The Reporter, 19 (2006)
A new selective preparation of 4H-chromenes by reaction of alkyl cyanoacetate with 3, 5-dibromosalicylaldehyde in the presence of ammonium acetate.
FUJIMOTO A and SAKURAI A.
Synthesis, 1977(12), 871-872 (1977)
Selective inhibition of benzyl ether hydrogenolysis with Pd/C due to the presence of ammonia, pyridine or ammonium acetate.
Sajiki H.
Tetrahedron Letters, 36(20), 3465-3468 (1995)
Eagleson M.
Concise Encyclopedia Chemistry, 65-65 (1994)
Reactions of phenanthraquinone and retenequinone with aldehydes and ammonium acetate in acetic acid solution1.
Steck EA and Day AR.
Journal of the American Chemical Society, 65(3), 452-456 (1943)

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