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Merck
CN

388807

3-(N,N-Dimethylpalmitylammonio)propanesulfonate

97%

Synonym(s):

3-(N,N-Dimethylhexadecylammonio)propanesulfonate, 3-(Palmityldimethylammonio)propanesulfonate, N-Hexadecyl-N,N-dimethyl-3-ammonio-1-propanesulfonate, Palmityl sulfobetaine, SB3-16, Zwittergent® 3-16

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About This Item

Linear Formula:
CH3(CH2)15N+(CH3)2CH2CH2CH2SO3-
CAS Number:
2281-11-0
Molecular Weight:
391.65
EC Number:
218-918-7
UNSPSC Code:
12352103
PubChem Substance ID:
329755801
Beilstein/REAXYS Number:
4149854
MDL number:
MFCD00036911

Key Documents

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InChI key

TUBRCQBRKJXJEA-UHFFFAOYSA-N

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

SMILES string

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

assay

97%

Legal Information

Zwittergent is a registered trademark of Merck KGaA, Darmstadt, Germany

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

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
10903BR
06125BS
02516AZ
01728JR

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Wan Cao et al.
Journal of chromatography. A, 1358, 277-284 (2014-07-23)
A rapid zwitterionic microemulsion electrokinetic chromatography (ZI-MEEKC) approach coupled with light-emitting-diode-induced fluorescence (LED-IF, 480nm) detection was proposed for the analysis of flavonoids. In the optimization process, we systematically investigated the separation conditions, including the surfactants, cosurfactants, pH, buffers and fluorescence
Francisco J Prado-Prado et al.
Bioorganic & medicinal chemistry, 18(6), 2225-2231 (2010-02-27)
There are many of pathogen parasite species with different susceptibility profile to antiparasitic drugs. Unfortunately, almost QSAR models predict the biological activity of drugs against only one parasite species. Consequently, predicting the probability with which a drug is active against

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