n phenyl 1 naphthylamine

    n phenyl 1 naphthylamine,

    N-Phenylnaphthalen-1-amine - Wikipedia

    N -Phenylnaphthalen-1-amine. N-Phenylnaphthalen-1-amine ( NPN) is a nonpolar, hydrophobic molecule with the chemical formula C 16NH 13. This molecule is most notable for its binding affinity in mouse major urinary protein (MUP). This ligand has the greatest binding affinity of all MUP binding ligand discovered,.

    N-Phenyl-1-naphthylamine CAS#: 90-30-2

    N-Phenyl-1-naphthylamine neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, …

    N--1-_ - baike.baidu

    N--1-(N-phenyl-1-naphthylamine),N--α-,,A。,、、、、、,,。,,。、。

    Synthesis of n-phenyl-2-naphthylamine - PrepChem

    Feb 24, 2016· Preparation of n-phenyl-2-naphthylamine. In a round-bottomed flask fitted with a thermometer and a vertical tube, a mixture of 143 grams (1.0 mole) of 1-naphthylamine, 175 grams of aniline, and 3 grams of sulfanilic acid is boiled vigorously for 42 hours.

    N-Phenyl-1-naphthylamine | C16H13N - PubChem

    N-Phenyl-1-naphthylamine's production and use as an antioxidant in various lubrication oils and as both a protective agent and antioxidant in rubber and rubber mixtures for various products, including tires, may result in its release to the environment thorugh various waste streams.

    n phenyl 1 naphthylamine,

    N-Phenyl-1-Naphthylamine/N-Phenyl-2-Naphthylamine - osha

    N-Phenyl-1-naphthylamine is used in the production of dyes and other organic chemicals, and also as a rubber antioxidant. N-Phenyl-2-naphthylamine is primarily used as an antioxidant in rubber processing. It is also used as a stabilizer in electrical-insulating enamels and as an antioxidant in other polymers, in greases, and in lubricating and transformer oils.

    n phenyl 1 naphthylamine,

    2-NAPHTHYLAMINE - NCBI Bookshelf

    1.2. Uses. 2-Naphthylamine formerly was used commercially as an intermediate in the manufacture of dyes, as an antioxidant in the rubber industry, and to produce 2-chloronaphthalene ().Because of its carcinogenicity, the manufacture and use of 2-naphthylamine have been prohibited in the European Union (EU) since 1998, in Italy since 1960, in the United Kingdom since 1952, and in Switzerland .

    N-PHENYL-2-NAPHTHYLAMINE | CAMEO Chemicals | NOAA

    N-PHENYL-2-NAPHTHYLAMINE may react with strong oxidizing agents (NTP, 1992). Neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides.

    N-Phenyl-1-naphthylamine - Santa Cruz Biotechnology

    its limited mineralization in soil, N-phenyl-1-naphthylamine is presumed to have geoaccumulation potential. The probability of infiltration into groundwater is low. Based upon studies with Daphnia and fish and its measured log Kow of 4.2, N-phenyl-1-naphthylamine is expected to have a moderate potential for bioaccumulation.

    Synthesis of n-phenyl-2-naphthylamine - PrepChem

    Feb 24, 2016· Preparation of n-phenyl-2-naphthylamine. In a round-bottomed flask fitted with a thermometer and a vertical tube, a mixture of 143 grams (1.0 mole) of 1-naphthylamine, 175 grams of aniline, and 3 grams of sulfanilic acid is boiled vigorously for 42 hours.

    n phenyl 1 naphthylamine,

    N-Phenyl-1-naphthylamine - Santa Cruz Biotechnology

    log Kow = 4.2 Based upon its physical/chemical properties, the distribution of N-phenyl-1-naphthylamine in the environment, predicted on the basis of a Level II fugacity model, was approximately 36% to soil, 34% to sediment, 29% to water, and less than 1% each to air, suspended sediment, and biota.

    N-Phenyl-1-naphthylamine reagent grade, 98% | Sigma-Aldrich

    N-Phenyl-1-naphthylamine can be used as fluorescent probe for the determination of critical micelle concentration of surfactants. N-Phenyl-1-naphthylamine was used in a method for determination of the concentration of organolithium and organomagnesium reagents.

    1-Naphthalenamine, N-phenyl- - webbook.nist

    IUPAC Standard InChIKey: XQVWYOYUZDUNRW-UHFFFAOYSA-N; CAS Registry Number: 90-30-2; Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file The 3d structure may be viewed using Java or Javascript.

    N-Phenyl-1-naphthylamine | Sigma-Aldrich

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

    N-Phenyl-1-naphthylamine 90-30-2 | TCI America

    [N-Phenyl-1-naphthylamine] [90-30-2] | Buy and find out price and availability, MSDS, properties of TCI's high quality specialty chemicals.

    1-Naphthalenamine, N-phenyl- - webbook.nist

    IUPAC Standard InChIKey: XQVWYOYUZDUNRW-UHFFFAOYSA-N; CAS Registry Number: 90-30-2; Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file The 3d structure may be viewed using Java or Javascript.

    1-Naphthylamine - Wikipedia

    1-Naphthylamine. 1-Naphthylamine is an aromatic amine derived from naphthalene. It can cause bladder cancer (transitional cell carcinoma). It crystallizes in colorless needles which melt at 50 °C. It possesses a disagreeable odor, sublimes readily, and turns brown on exposure to air. It is the precursor to a …

    N-Phenyl-1-Naphthylamine/N-Phenyl-2-Naphthylamine - osha

    N-Phenyl-1-naphthylamine is used in the production of dyes and other organic chemicals, and also as a rubber antioxidant. N-Phenyl-2-naphthylamine is primarily used as an antioxidant in rubber processing. It is also used as a stabilizer in electrical-insulating enamels and as an antioxidant in other polymers, in greases, and in lubricating and transformer oils.

    N-PHENYL-1-NAPHTHYLAMINE | CAMEO Chemicals | NOAA

    N-PHENYL-1-NAPHTHYLAMINE neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides.

    Substance Name: N-Phenyl-1-naphthylamine

    90-30-2 - XQVWYOYUZDUNRW-UHFFFAOYSA-N - N-Phenyl-1-naphthylamine - Similar structures search, synonyms, formulas, resource links, and other chemical information.

    N-Phenyl-1-naphthylamine CAS 90-30-2 | 821003

    N-Phenyl-1-naphthylamine MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

    n phenyl 1 naphthylamine,

    N-Phenyl-1-naphthylamine | CAS 90-30-2 | SCBT - Santa Cruz .

    Buy N-Phenyl-1-naphthylamine (CAS 90-30-2), a fluorescent probe, from Santa Cruz Biotechnology. Molecular Formula: C16H13N, Molecular Weight: 219.29

    N-Phenyl-1-naphthylamin – Wikipedia

    N-Phenyl-1-naphthylamin ist als technisches Produkt ein brennbarer, schwer entzündbarer, schuppiger, rotvioletter Feststoff mit schwach aromatischem Geruch, der praktisch unlöslich in Wasser ist. Die Verbindung in Reinform liegt in Form von zitronengelben Nadeln oder Prismen vor.

    1-naphthylamine | Spectrum

    1-Naphthylamine, also known as a-Naphthylamine, is an aromatic amine. Ungraded products supplied by Spectrum are indicative of a grade suitable for general industrial use or research purposes and typically are not suitable for human cons

    n phenyl 1 naphthylamine,

    N-Phenyl-1-Naphthylamine - N Phenyl-1-Naphthylamine .

    N-Phenyl-1-Naphthylamine. Our product range includes a wide range of n phenyl-1-naphthylamine, dye intermediates, c16h13n dye intermediates and phenyl-1-naphthylamine pure.

    Synthesis of 1-naphthylamine - PrepChem

    Jan 04, 2016· Synthesis of 1-naphthylamine. Preparation of 1-naphthylamine. 200 g of iron turnings, 100 g water, and 10 ml of 30% hydrochloric acid are placed to a beaker which is fitted with a stirrer.

    n phenyl 1 naphthylamine,

    N-phenyl-1-naphthylamine - Wikidata

    N-PHENYL-1-NAPHTHYLAMINE (English) retrieved. 19 October 2016. chemical formula. C₁₆H₁₃N. 1 reference. stated in. PubChem. PubChem CID. 7013. language of work or name. English. . N-phenyl-1-napthylamine (English) retrieved. 19 November 2016. PDB structure ID. 3S0B. 1 reference. stated in. Protein Data Bank. PDB structure ID. 3S0B .

    N-PHENYL-2-NAPHTHYLAMINE | CAMEO Chemicals | NOAA

    N-PHENYL-2-NAPHTHYLAMINE may react with strong oxidizing agents (NTP, 1992). Neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides.

    N-Phenyl-1-naphthylamine 90-30-2 | TCI America

    [N-Phenyl-1-naphthylamine] [90-30-2] | Buy and find out price and availability, MSDS, properties of TCI's high quality specialty chemicals.

    Phenyl-1-naphthylamine, n- (CICADS) - IPCS INCHEM

    Although data concerning the formation of this metabolite are not available for N-phenyl-1-naphthylamine, it should be noted that, based on its chemical structure, it is unlikely that N-phenyl-1-naphthylamine is metabolized to 2-naphthylamine.

    N-PHENYL-1-NAPHTHYLAMINE [N-(1-NAPHTHYL)ANILINE]

    N-Phenyl-1-naphthylamine is a lipophilic white to slight brownish crystalline powder that is used as an antioxidant in various in rubbers and lubrication oils. It is also used as an itermediate for vulcanization accelerators, dyes and other organic chemicals.

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