Skip to Content
Merck
All Photos(1)

Key Documents

40232

Sigma-Aldrich

N-Dodecyl-N,N-dimethyl-3-ammonio-1-propanesulfonate

≥97.0% (dried material, CHN)

Synonym(s):

3-(N,N-Dimethyldodecylammonio)propanesulfonate, 3-(N,N-Dimethyllaurylammonio)propanesulfonate, 3-(Dodecyldimethylammonio)propanesulfonate, 3-(Lauryldimethylammonio)propanesulfonate, Dodecyldimethyl(3-sulfopropyl)ammonium hydroxide inner salt, Lauryl sulfobetaine, SB3-12

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3(CH2)11N+(CH3)2CH2CH2CH2SO3-
CAS Number:
Molecular Weight:
335.55
Beilstein:
4145308
EC Number:
MDL number:
UNSPSC Code:
12161900
eCl@ss:
32190102
PubChem Substance ID:
NACRES:
NA.25

description

zwitterionic

Assay

≥97.0% (dried material, CHN)

form

powder

mol wt

micellar avg mol wt 18,500

aggregation number

55

ign. residue

≤0.1%

loss

≤1% loss on drying, 110 °C

CMC

2-4 mM (20-25°C)

cation traces

Ca: ≤20 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤50 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Na: ≤150 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg

application(s)

detection

SMILES string

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

InChI

1S/C17H37NO3S/c1-4-5-6-7-8-9-10-11-12-13-15-18(2,3)16-14-17-22(19,20)21/h4-17H2,1-3H3

InChI key

IZWSFJTYBVKZNK-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

N-Dodecyl-N,N-dimethyl-3-ammonio-1-propanesulfonate has been used as a component of trypsin buffer for the dialysis of protein solution.

Other Notes

Zwitterionic surfactant which effectively solubilizes cardiac 5′-nucleotidase

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Paul L Sorgen et al.
Biochemistry, 41(1), 31-41 (2002-01-05)
The light harvesting 1 antenna (LH1) complex from Rhodobacter sphaeroides funnels excitation energy to the photosynthetic reaction center. Our ultimate goal is to build up the structure of LH1 from structures of its individual subunits, much as the antenna can
Abhay H Pande et al.
Biochemistry, 43(46), 14653-14666 (2004-11-17)
Mammalian 5-lipoxygenase (5-LO) catalyzes the conversion of arachidonic acid (AA) to leukotrienes, potent inflammatory mediators. 5-LO is activated by a Ca(2+)-mediated translocation to membranes, and demonstrates the characteristic features of interfacially activated enzymes, yet the mechanism of membrane binding of
R R Julian et al.
Journal of the American Chemical Society, 123(15), 3577-3583 (2001-07-27)
The discovery of several new unusually stable aggregates of arginine that are intermolecularly bound by salt bridges is reported. Quadrupole ion-trap mass spectrometry provides evidence for the stability of arginine in the zwitterionic state, where the protonated guanidinium group of
J W Anderson et al.
Biochemistry, 39(40), 12200-12209 (2000-10-04)
Bacterial cell walls are cross-linked in the final step of biosynthesis by specific D-alanyl-D-alanine(DD)-peptidases/transpeptidases. The natural substrates of these enzymes should therefore be segments of peptidoglycan, but high specificity for such structures has yet to be demonstrated. The binding of
Masahiro Yoshizawa-Fujita et al.
The journal of physical chemistry. B, 114(49), 16373-16380 (2010-11-23)
We describe zwitterion, 3-(1-butyl-1H-imidazol-3-ium-3-yl)propane-1-sulfonate (Bimps), mixtures with 1,1,1-trifluoro-N-(trifluoromethylsulfonyl)methanesulfoneamide (HN(Tf)(2)) as new proton transport electrolytes. We report proton transport mechanisms in the mixtures based on results from several methods including thermal analyses, the complex-impedance method, and the pulsed field gradient spin

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service