nn dimethylaniline n oxide c8h11no chemspider

nn-dimethylaniline-n-oxide | C8H11NO | ChemSpider

Simple Structure Advanced History Comment on this record 3D nn-dimethylaniline-n-oxide Molecular Formula CHNO Average mass 137.179 Da Monoisotopic mass 137.084061 Da ChemSpider ID 925 More details: Names Properties Searches Spectra Vendors Articles More Names and Synonyms Database ID (s)

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N,N-Dimethylaniline N-oxide | C8H11NO | CID 950 - PubChem

Molecular Formula C8H11NO Synonyms N,N-Dimethylaniline N-oxide Dimethylaniline N-oxide 874-52-2 N,N-dimethylaniline-N-oxide Benzenamine, N,N-dimethyl-, N-oxide View More... Molecular Weight 137.18 g/mol Computed by PubChem 2.1 (PubChem release 2021.05.07) Dates Create: 2004-09-16 Modify: 2023-07-01 Description

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PQR | Nn-dimethylaniline-n-oxide - University of Pittsburgh

You are viewing an interactive 3D depiction of the molecule nn-dimethylaniline-n-oxide (C8H11NO) from the PQR. PubChem ChemSpider: DOI: 10.17614/Q4HX15X8V; 10/f29t8r;

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N,N-Dimethylaniline | C8H11N | ChemSpider

Simple Structure Advanced History Comment on this record 3D N,N-Dimethylaniline Molecular Formula CHN Average mass 121.180 Da Monoisotopic mass 121.089149 Da ChemSpider ID 924 More details: Featured data source Names Properties Searches Spectra Vendors Articles More Names and Synonyms Database ID (s)

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N,N-Dimethylaniline | C8H11N | CID 949 - PubChem

N,N-Dimethylaniline | C8H11N | CID 949 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities

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N,N-DIMETHYLANILINE N-OXIDE - National Center for Advancing

National Center for Advancing Translational Sciences (NCATS), 6701 Democracy Boulevard, Bethesda MD 20892-4874 ? 301-594-8966

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N,N-dimethylaniline-N-oxide hydrochloride | C8H12ClNO | CID

N,N-dimethylaniline-N-oxide hydrochloride | C8H12ClNO | CID 85859010 - structure, chemical names, physical and chemical properties, classification, patents

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SAFETY DATA SHEET - Fisher Sci

N,N-Dimethylaniline ( DMA) is an organic chemical compound, a substituted derivative of aniline. It consists of a tertiary amine, featuring dimethylamino group attached to a phenyl group. This oily liquid is colourless when pure, but commercial samples are often yellow. It is an important precursor to dyes such as crystal violet .

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N,N-Dimethylaniline | C8H11N | MD Topology | NMR | X-Ray

N,N-Dimethylaniline | C8H11N | MD Topology | NMR | X-Ray The Automated Topology Builder (ATB) and Repository is intended to facilitate the development of molecular force fields for Molecular Dynamics or Monte Carlo simulations of biomolecular systems.

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The metabolism of N,N-dimethylaniline by isolated rat

The N-glucuronidation of the secondary N-alkylarylamine, N-methylaniline, by rat hepatocytes represents a quantitatively important and previously uncharacterized route of metabolism in these cells. Further studies are, however, required to identify this metabolite unequivocally as the N-glucuronide of N-methylaniline. Publication types

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N,N-DIMETHYLANILINE | CAMEO Chemicals | NOAA

Chemical Identifiers What is this information? NFPA 704 (NFPA, 2010) General Description A yellow to brown colored oily liquid with a fishlike odor. Less dense than water and insoluble in water. Flash point 150°F. Toxic by ingestion, inhalation, and skin absorption. Used to make dyes and as a solvent. Hazards What is this information?

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N,N-dimethylaniline hydrochloride | C8H12ClN - PubChem

N,N-dimethylaniline hydrochloride | C8H12ClN | CID 79987 - structure, chemical names, physical and chemical properties, classification, patents, literature

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SAFETY DATA SHEET - Fisher Sci

N,N-dimethylaniline-N-oxide hydrochloride | C8H12ClNO | CID 85859010 - structure, chemical names, physical and chemical properties, classification, patents

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Synthesis of Halogenated Anilines by Treatment of N,N

The N-glucuronidation of the secondary N-alkylarylamine, N-methylaniline, by rat hepatocytes represents a quantitatively important and previously uncharacterized route of metabolism in these cells. Further studies are, however, required to identify this metabolite unequivocally as the N-glucuronide of N-methylaniline. Publication types

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N,N-Dimethylaniline | C8H11N | MD Topology | NMR | X-Ray

The Automated Topology Builder (ATB) and Repository is intended to facilitate the development of molecular force fields for Molecular Dynamics or Monte Carlo simulations of biomolecular systems.

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Anilinic N-Oxides Support Cytochrome P450-Mediated N

3-Methoxy-N-methylaniline | C8H11NO | CID 84349 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological

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N-(2,6-dimethylphenyl)hydroxylamine | C8H11NO | CID 145679

Molecular Formula C8H11NO Synonyms N- (2,6-dimethylphenyl)hydroxylamine 3096-63-7 Benzenamine, N-hydroxy-2,6-dimethyl- CCRIS 5431 2,6-Dimethylphenylhydroxylamine View More... Molecular Weight 137.18 g/mol Computed by PubChem 2.1 (PubChem release 2021.05.07) Dates Create: 2005-08-08 Modify: 2023-06-03 1 Structures 1.1 2D Structure Structure Search

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Studies on the mechanism of hepatic microsomal N-oxide

N,N-Dimethylaniline ( DMA) is an organic chemical compound, a substituted derivative of aniline. It consists of a tertiary amine, featuring dimethylamino group attached to a phenyl group. This oily liquid is colourless when pure, but commercial samples are often yellow. It is an important precursor to dyes such as crystal violet .

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N,N-Dimethylaniline | The Merck Index Online

Molecular Formula: C 8 H 11 N Molecular Weight: 121.18 Percent Composition: C 79.29%, H 9.15%, N 11.56%

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