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40103

Sigma-Aldrich

N,N-Dimethyldecylamine N-oxide

≥99.0% (NT)

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Synonym(s):
1-Decanamine, N,N-dimethyl-, N-oxide, N,N-dimethyldecan-1-amine oxide, DDAO
Linear Formula:
CH3(CH2)9N(O)(CH3)2
CAS Number:
Molecular Weight:
201.35
Beilstein:
2352550
EC Number:
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.26

description

non-ionic

Quality Level

Assay

≥99.0% (NT)

form

powder

mol wt

201.35 g/mol

impurities

≤0.03% peroxides (as H2O2)

anion traces

sulfate (SO42-): ≤50 mg/kg

cation traces

Ca: ≤500 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: ≤50 mg/kg
Mn: ≤5 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg

storage temp.

2-8°C

SMILES string

CCCCCCCCCC[N+](C)(C)[O-]

InChI

1S/C12H27NO/c1-4-5-6-7-8-9-10-11-12-13(2,3)14/h4-12H2,1-3H3

InChI key

ZRKZFNZPJKEWPC-UHFFFAOYSA-N

General description

N,N-Dimethyldecylamine N-oxide is a nonionic surfactant.

Application

N,N-Dimethyldecylamine N-oxide is suitable for use as a component of dihydroorotate dehydrogenase (DHODH) protein solution to prepare drops for the crystallization of DHODH-piperine complexes. It is also suitable for use as a nonionic surfactant to study the nonreversible adsorption phenomena at the graphite/water interface by pulsed-flow microcalorimetry.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Zehui Liu et al.
Biochemical pharmacology, 177, 114000-114000 (2020-05-01)
Multiple sclerosis (MS) is the most popular chronic and debilitating inflammatory disease of the central nervous system (CNS) that remains incurable. Dihydroorotate dehydrogenase (DHODH) is critical to the activity of T lymphocytes and represents a potential therapeutic target for MS.
Zoltán Király et al.
Langmuir : the ACS journal of surfaces and colloids, 21(11), 5047-5054 (2005-05-18)
The formation of half-cylindrical surfactant aggregates at the graphite/aqueous solution interface is templated by an ordered monolayer of molecules disposed parallel to the graphite basal plane. Beyond a critical alkyl chain length, monolayer formation is effectively irreversible. Since enthalpic interactions
NMR studies of binary surfactant mixture thermodynamics: molecular size model for asymmetric activity coefficients
Eads CD and Robosky LC
Langmuir, 15(8), 2661-2668 (1999)
Cindy S Tran et al.
PLoS pathogens, 10(11), e1004479-e1004479 (2014-11-07)
Clinical infections by Pseudomonas aeruginosa, a deadly Gram-negative, opportunistic pathogen of immunocompromised hosts, often involve the formation of antibiotic-resistant biofilms. Although biofilm formation has been extensively studied in vitro on glass or plastic surfaces, much less is known about biofilm
Nathan H Roy et al.
Journal of virology, 88(13), 7645-7658 (2014-04-25)
During cell-to-cell transmission of HIV-1, viral and cellular proteins transiently accumulate at the contact zone between infected (producer) and uninfected (target) cells, forming the virological synapse. Rearrangements of the cytoskeleton in producer and target cells are required for proper targeting

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