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T7763

Sigma-Aldrich

3-(N,N-Dimethylmyristylammonio)propanesulfonate

≥99% (TLC)

Synonym(s):

3-(N,N-Dimethyltetradecylammonio)propanesulfonate, 3-(Myristyldimethylammonio)propanesulfonate, N-Tetradecyl-N,N-dimethyl-3-ammonio-1-propanesulfonate, Myristyl sulfobetaine, SB3-14

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About This Item

Linear Formula:
CH3(CH2)13N+(CH3)2CH2CH2CH2SO3-
CAS Number:
14933-09-6
Molecular Weight:
363.60
Beilstein:
6419727
EC Number:
239-003-9
MDL number:
MFCD00036910
UNSPSC Code:
12161900
PubChem Substance ID:
24900472
NACRES:
NA.25

description

zwitterionic

Assay

≥99% (TLC)

mol wt

micellar avg mol wt 30,200

aggregation number

83

technique(s)

electrophoresis: suitable

conductivity

≤20 μmho per cm at 24 °C (0.1 M aqueous solution)

CMC

0.1-0.4 mM (20-25°C)

solubility

H2O: 50 mg/mL

application(s)

detection

SMILES string

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

InChI

1S/C19H41NO3S/c1-4-5-6-7-8-9-10-11-12-13-14-15-17-20(2,3)18-16-19-24(21,22)23/h4-19H2,1-3H3

InChI key

BHATUINFZWUDIX-UHFFFAOYSA-N

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General description

3-(N,N-Dimethylmyristylammonio)propanesulfonate is a zwitterionic surfactant used in various electrostatic ion chromatography techniques.3
Zwitterionic detergent.

Application

3-(N,N-Dimethylmyristylammonio)propanesulfonate has been used in a study to assess a method for quantifying perchlorate in biological samples using CE and capacitively coupled contactless conductivity detection.1 It has also been used in a study to investigate an approach for establishing adsorbents for elimination of water-soluble organic dyes.2

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

>230.0 °F

Flash Point(C)

> 110 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

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C A Minetti et al.
The Journal of biological chemistry, 273(39), 25329-25338 (1998-09-17)
PorB proteins constitute the vast majority of channels in neisserial outer membranes and can be subdivided within meningococcal strains into two distinct and mutually exclusive families that are designated as class 2 and class 3 proteins. We recently characterized the
D Grenier
Microbiology (Reading, England), 142 ( Pt 6), 1537-1541 (1996-06-01)
The ability of Prevotella intermedia to bind type I collagen was investigated. A simple method in which bacterial cells were allowed to attach to collagen-coated microtitre plate wells was used to characterize the activity. All strains of P. intermedia tested
Milo S Johnson et al.
eLife, 10 (2021-01-20)
Laboratory experimental evolution provides a window into the details of the evolutionary process. To investigate the consequences of long-term adaptation, we evolved 205 Saccharomyces cerevisiae populations (124 haploid and 81 diploid) for ~10,000,000 generations in three environments. We measured the
D Russell-Harde et al.
Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research, 15(1), 31-37 (1995-01-01)
A new method for purifying human interferon-beta SER17 from E. coli-derived inclusion bodies has been developed. This procedure eliminates the need for strong denaturants, such as sodium dodecyl sulfate or chaotropes. The procedure makes use of a nondenaturing detergent and
Qian Guan et al.
Electrophoresis, 33(2), 379-387 (2012-01-10)
The use of mixtures of ionic and zwitterionic surfactants in poly(dimethylsiloxane) (PDMS) microchips is reported. The effect of surfactant concentration on electroosmotic flow (EOF) was studied for a single anionic surfactant (sodium dodecyl sulfate, SDS), a single zwitterionic surfactant (N-tetradecylammonium-N,N-dimethyl-3-ammonio-1-propanesulfonate
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