ChemicalBook--->CAS DataBase List--->66455-29-6

66455-29-6

66455-29-6 Structure

66455-29-6 Structure
IdentificationBack Directory
[Name]

N-DODECYL-N,N-DIMETHYLGLYCINE
[CAS]

66455-29-6
[Synonyms]

BC-12
Flavol BMK
empigen BB
EmpigenBB/P
EMPIGEN BB(R)
EMPIGEN(R) BB
Mirataine H 30
Petrostep B 1235
Geronol CF/AS 30
Tego-Betain A 1214
Geronol CF/AS 30HL
EMPIGEN?BBdetergen
EMPIGEN BB DETERGENT
empigenbb(r)detergent
EMPIGEN(R) BB DETERGENT
DODECYL DIMETHYL BETAINE
C12-14-alkyldimethylbetaine
Betaine, C12--Alkyldimethyl-
Betaines,C12-14-alkyldimethyl
N-DODECYL-N,N-DIMETHYLGLYCINE
C12-14-Alkyldimethyl-Betaines
LAURYL DIMETHYLAMINOACETIC ACID
Dimethylalkyl(C=12~14), betaines
3-AZONIA-3,3-DIMETHYLPENTADECANOATE
N,N-DIMETHYL-N-DODECYLGLYCINE BETAINE
N-(ALKYL C10-C16)-N,N-DIMETHYLGLYCINE BETAINE
3-[(3- Product Name:N-DODECYL-N,N-DIMETHYLGLYCINE
N,N-Dimethyl-N-dodecylglycine betaine, N-(Alkyl C10-C16)-N,N-dimethylglycine betaine
[EINECS(EC#)]

931-700-2
[Molecular Formula]

C16H33NO2
[MDL Number]

MFCD00084742
[MOL File]

66455-29-6.mol
[Molecular Weight]

271.44
Chemical PropertiesBack Directory
[density ]

1.04 g/mL at 20 °C
[vapor pressure ]

0Pa at 25℃
[form ]

Paste
[λmax]

λ: 417 nm Amax: ≤0.055
λ: 441 nm Amax: ≤0.037
[BRN ]

3670807
[InChI]

1S/C16H33NO2/c1-4-5-6-7-8-9-10-11-12-13-14-17(2,3)15-16(18)19/h4-15H2,1-3H3
[InChIKey]

DVEKCXOJTLDBFE-UHFFFAOYSA-N
[SMILES]

CCCCCCCCCCCC[N+](C)(C)CC([O-])=O
[LogP]

-0.4 at 20℃ and pH6.86
[Surface tension]

36.1mN/m at 1g/L and 20℃
[Dissociation constant]

3.64 at 20℃
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

1
[REACH Registrations]

Active
[Storage Class]

10 - Combustible liquids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

Empigen BB is a zwitterionic detergent compatible with anionic, non-ionic, cationic and other amphoteric surfactants.

Empigen BB is a useful detergent that has been used in the solubilization of membrane proteins and biochemical analysis of keratins. It not only helps to solubilize bigger amounts of protein but it also maintains antibody reactivity. It has been also used in the purification of leucine-rich repeat kinase 2 (LRRK2) in Escherichia coli during research in Parkinson′s disease. The use of Empigen in the preparation of viral antigens is being increasing due to its effectivity in giving greater antibody responses.
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