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40772

3-(N,N-Dimethylmyristylammonio)propanesulfonate

≥98.0% (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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$133.00

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$469.00

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About This Item

Linear Formula:
CH3(CH2)13N+(CH3)2CH2CH2CH2SO3-
CAS Number:
14933-09-6
Molecular Weight:
363.60
Beilstein/REAXYS Number:
6419727
EC Number:
239-003-9
MDL number:
MFCD00036910
UNSPSC Code:
12161900
PubChem Substance ID:
329755943
NACRES:
NA.25

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description

zwitterionic

Quality Level

200

assay

≥98.0% (TLC)

form

powder

mol wt

micellar avg mol wt 30,200

aggregation number

83

technique(s)

nucleic acid detection: suitable
protein purification: suitable
protein quantification: suitable

CMC

0.1-0.4 mM (20-25°C)

mp

246 - 248  °C

solubility

water: 100 g/L at 20 °C

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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1 of 4

This Item
T0807H6883T7763
3-(N,N-Dimethylmyristylammonio)propanesulfonate ≥98.0% (TLC)

Sigma-Aldrich

40772

3-(N,N-Dimethylmyristylammonio)propanesulfonate

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

Sigma-Aldrich

T0807

3-(N,N-Dimethylmyristylammonio)propanesulfonate

3-(N,N-Dimethylpalmitylammonio)propanesulfonate ≥98% (TLC)

Sigma-Aldrich

H6883

3-(N,N-Dimethylpalmitylammonio)propanesulfonate

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

Sigma-Aldrich

T7763

3-(N,N-Dimethylmyristylammonio)propanesulfonate

technique(s)

nucleic acid detection: suitable, protein quantification: suitable, protein purification: suitable

technique(s)

electrophoresis: suitable, ion chromatography: suitable

technique(s)

electrophoresis: suitable, mass spectrometry (MS): suitable, thin layer chromatography (TLC): suitable

technique(s)

electrophoresis: suitable

assay

≥98.0% (TLC)

assay

≥99% (TLC)

assay

≥98% (TLC)

assay

≥99% (TLC)

aggregation number

83

aggregation number

83

aggregation number

155

aggregation number

83

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

CMC

0.1-0.4 mM (20-25°C)

CMC

0.1-0.4 mM (20-25°C)

CMC

0.01-0.06 mM (20-25°C)

CMC

0.1-0.4 mM (20-25°C)

mol wt

micellar avg mol wt 30,200

mol wt

micellar avg mol wt 30,200

mol wt

micellar avg mol wt 60,700

mol wt

micellar avg mol wt 30,200

General description

Zwitterionic detergent.

Other Notes

Zwitterionic surfactant which effectively solubilises cardiac 5′-nucleotidase[1]; Micorsomal proteins[2]; H+-ATPase from corn roots[3]

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_germany

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
WXBF6883V
WXBF5338V
WXBF3417V
WXBF4407V
WXBF0899V

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A.B. Bennett et al.
Membrane Biol., 75, 21-21 (1983)
E.N.C. Mills et al.
Biochimica et Biophysica Acta, 734, 160-160 (1984)
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
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
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
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