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Merck
CN

40103

N,N-Dimethyldecylamine N-oxide

≥99.0% (NT)

Synonym(s):

1-Decanamine, N,N-dimethyl-, N-oxide, N,N-dimethyldecan-1-amine oxide, DDAO

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About This Item

Linear Formula:
CH3(CH2)9N(O)(CH3)2
CAS Number:
2605-79-0
Molecular Weight:
201.35
UNSPSC Code:
12352116
NACRES:
NA.26
PubChem Substance ID:
57649925
EC Number:
220-020-5
Beilstein/REAXYS Number:
2352550
MDL number:
MFCD00082523

Key Documents

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Product Name

N,N-Dimethyldecylamine N-oxide, ≥99.0% (NT)

InChI key

ZRKZFNZPJKEWPC-UHFFFAOYSA-N

InChI

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

SMILES string

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

description

non-ionic

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

Quality Level

100

Related Categories

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.

General description

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

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

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG1980
BCCG8186
BCBH6039V
49253/1
049253/1

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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)
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
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.
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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