N-phenyl-1-naphthylamine and N-phenyl-2-naphthylamine in mice. Cancer research, 44:3098-3100. Xuanxian X, Wolff T (1992) Metabolism of N-phenyl-2-naphthylamine and N-phenyl-1-naphthylamine by rat hepatic microsomes and hepatocytes. Journal of environmental science, 4:74-83. Zeiger E, Anderson B, Haworth S, Lawlor T, Mortelmans K (1988)
What is the abbreviation for N-phenyl-1-naphthylamine? What does NPN stand for? NPN abbreviation stands for N-phenyl-1-naphthylamine.
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SAFETY DATA SHEET NESTE TURBINE GT 46 SECTION 1: Identification of the substance/mixture and of the company/undertaking 1.1. Product identifier Product name NESTE TURBINE GT 46 Product number ID 16794 Internal identification 3097 1.2. Relevant identified uses of the substance or mixture and uses advised against Identified uses Lubricant. 1.3.
TRiiSO distributes a wide range of antioxidants that allow formulators to produce high quality lubricants. Antioxidants protect lubricants from thermal degradation by scavenging free radicals, thereby preventing the oxidation of the lubricant. TRiiSO's portfolio of antioxidants include both phenolic and aminic varieties.
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Metabolic dephenylation of the rubber antioxidant N-phenyl-2-naphthylamine to carcinogenic 2-naphthylamine in rats Article in Archives of Toxicology 87(7) · February 2013 with 26 Reads
N-Phenyl-alpha-naphthylamine - chemical information, properties, structures, articles, patents and more chemical data.
Heating N-phenyl-1-naphthylamine with epichlorohydrin gives N-phenyl-N-(3-chloro-2-hydroxy-propyl)-1-naphthylamine, which cyclizes with the participation of the phenyl ring.
N-Phenyl-2-naphthylamine is probably released to the environment in waste streams from its production and use. In the atmosphere, it should exist in the vapor and particulate phases. Vapor phase N-phenyl-2-naphthylamine is expected to degrade rapidly (estimated half-life of 55 minutes) by reaction with photochemically produced hydroxyl radicals ...
PANA (N-Phenyl-alpha-naphthylamine) is a high-purity product widely used as an antioxidant in petroleum products, synthetic lubricants, rubber products, and as an organic intermediate. Petroleum Products: greases, turbine oils, heat transfer fluids, crankcase lubricants, transformer oils, hydraulic and transmission fluids, and metal working fluids.
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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 variety of dyes.
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.
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NIOSH. At concentrations above the NIOSH REL, or where there is no REL, at any detectable concentration: (APF = 10,000) Any self-contained breathing apparatus that has a full facepiece and is operated in a pressure-demand or other positive-pressure mode
The anti-MRSA cephalosporin ceftobiprole is another β-lactam that is poorly recognized by MexB, MexD, and MexF in P. aeruginosa (Baum et al., 2009).Overexpression of these eﬄux pumps had only the marginal effect on the activity of ceftobiprole of a twofold increase of the minimum inhibitory concentration (MIC).
Predicted data is generated using the US Environmental Protection Agency's EPISuite™. Log Octanol-Water Partition Coef (SRC): Log Kow (KOWWIN v1.67 estimate) = 4.47 Log Kow (Exper. database match) = 4.20 Exper.
N-phenyl-1-naphthylamine is mutagenic in rodents. It impaired the rate of development of frog embryos and increased the incidence of abnormal forms. No studies have been identified on possible reproductive effects or lactation of it in humans. Section 12: Ecological Information Ecological Data for ADDITIN RC 7132 440D/1760S
Structure, properties, spectra, suppliers and links for: Octyl-phenyl-α-naphthylamine.
N-phenyl-1-naphthylamine - CAS # 90-30-2 Information provided on N-phenyl-1-naphthylamine (90-30-2) is for reference only and is subject to change. There is no warranty of accuracy or completeness of any information contained herein.
Search results for N-Phenyl-1-naphthylamine at Sigma-Aldrich. Compare Products: Select up to 4 products. *Please select more than one item to compare
POLYSORBATE STRUCTURE. The polysorbates are amphipathic, nonionic surfactants composed of fatty acid esters of polyoxyethylene sorbitan. 21 Polysorbate 20 (polyoxyethylene sorbitan monolaurate) and Polysorbate 80 (polyoxyethylene sorbitan monooleate) are the most common polysorbates currently used in formulation of protein biopharmaceuticals. 22 Their structures are shown in Figure 1.
N-Phenyl-1-naphthylamine for synthesis. CAS 90-30-2, pH (H₂O) neutral. - Find MSDS or SDS, a COA, data sheets and more information.
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.
On the Mode of Action of N -Phenyl-2-naphthylamine in Plants. ... Ecotoxicological standard tests assess toxic effects by exposing an organism to high concentrations over short, defined periods of ...
food-chain seems unlikely in view of the chemical's metabolism and extensive excretion. The acute toxicity of N-phenyl-1-naphthylamine in fish and Daphnia is high, with lowest reported no-observed-effect concentrations (NOECs) of 0.11 mg/litre (192 h) and 0.02 mg/litre (21 days), respectively.
Aminic Antioxidant - IRGANOX® L 06. ... -Ashless, high purity product with low volatility -Provides much lower sludging ...
N-Phenyl-1-naphthylamine is used in the production of dyes and other organic chemicals, and also as a rubber antioxidant. ( Ref. 5.12. N- Phenyl-2-naphthylamine is primarily used as an antioxidant in rubber processing.
N-Phenyl-1-naphthylamine | C16H13N | CID 7013 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological ...
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