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Merck

T0807

3-(N,N-Dimethylmyristylammonio)propanesulfonate

≥99% (TLC), BioXtra

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
UNSPSC Code:
12161900
NACRES:
NA.25
PubChem Substance ID:
24899915
EC Number:
239-003-9
Beilstein/REAXYS Number:
6419727
MDL number:
MFCD00036910

Key Documents

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Product Name

3-(N,N-Dimethylmyristylammonio)propanesulfonate, ≥99% (TLC), BioXtra

Quality Level

200

InChI key

BHATUINFZWUDIX-UHFFFAOYSA-N

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

SMILES string

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

description

zwitterionic

product line

BioXtra

assay

≥99% (TLC)

mol wt

micellar avg mol wt 30,200

aggregation number

83

technique(s)

electrophoresis: suitable
ion chromatography: suitable

impurities

≤0.0005% Phosphorus (P)
≤0.1% Insoluble matter

ign. residue

≤0.1%

CMC

0.1-0.4 mM (20-25°C)

solubility

H2O: 50 mg/mL, clear, colorless

anion traces

chloride (Cl-): ≤0.05%
sulfate (SO42-): ≤0.05%

cation traces

Al: ≤0.0005%
Ca: ≤0.001%
Cu: ≤0.0005%
Fe: ≤0.0005%
K: ≤0.005%
Mg: ≤0.0005%
NH4+: ≤0.05%
Na: ≤0.005%
Pb: ≤0.001%
Zn: ≤0.0005%

application(s)

detection

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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. It has also been used in a study to investigate an approach for establishing adsorbents for elimination of water-soluble organic dyes.

General description

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

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

>230.0 °F

flash_point_c

> 110 °C

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SLBZ4747
SLBM1591V
120M5328V
120M5328
058K5305

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A novel adsorbent obtained by inserting carbon nanotubes into cavities of diatomite and applications for organic dye elimination from contaminated water
Yu, H. and B. Fugetsu
Journal of Hazardous Materials, 177, 8-8 (2010)
H A Cook et al.
Analytical chemistry, 73(13), 3022-3027 (2001-07-27)
The retention mechanism of electrostatic ion chromatography (EIC) is currently under debate and is the focus of this paper. A comprehensive set of retention data has been obtained on a C18 column coated with the zwitterionic surfactant 3-(N,N-dimethylmyristylammonio)propanesulfonate used with
Yoshihiro Kuroda et al.
Journal of peptide science : an official publication of the European Peptide Society, 9(4), 212-220 (2003-05-03)
Pathogenic prion proteins (PrP(Sc)) are thought to be produced by alpha-helical to beta-sheet conformational changes in the normal cellular prion proteins (PrP(C)) located solely in the caveolar compartments. In order to inquire into the possible conformational changes due to the
Emmanuel Camors et al.
Journal of molecular and cellular cardiology, 40(1), 47-55 (2005-12-07)
Annexin A5 is a Ca2+ dependent phosphatidylserine binding protein mainly located in the T-tubules and sarcolemma of cardiomyocytes. Our objectives were to determine whether annexin A5 was associated with various protein(s) and whether such an association was modified in failing
A Blanchard et al.
Biochimie, 67(12), 1251-1256 (1985-12-01)
The extraction of proteins from the membrane of the mollicute (mycoplasma) Spiroplasma citri by sodium N-dodecyl-N,N-dimethyl-3-amino-1-propane sulfonate (SB12) and sodium N-tetradecyl-N,N-dimethyl-3-amino-1-propane sulfonate (SB14) was studied with electrophoretic methods. The membranes were prepared by osmotic lysis of the cells and depleted
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