2-Phenylaminonaphthalene Aceto PBN AgeRite Powder AK 1 AK 1 (stabilizer) Antioxidant 116 Antioxidant D Antioxidant PBN beta-Naphthylphenylamine Fenyl-beta-naftylamin (Czech) N-(2-Naphthyl)aniline Naftam 2 NCI-C02915 Neozon D Neozone Neozone D N-Fenyl-2-aminonaftalen (Czech) Nilox PbNa Noclizer D Nocrac D Nonox D N-Phenyl-2-naphthylamine N ...
Using an initial concn of 100 mg/L N-phenyl-2-naphthylamine, 0 %BOD was observed after a 2 week period in a biodegradation screening test using 30 mg/L sludge(1). N-Phenyl-2-naphthylamine, initial concn of 100 ppm, exhibited a 0-29 % Theoretical BOD in a Japanese MITI test after 14 days of incubation at 25 deg C(2).
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. As soon as the evolution of hydrogen has ceased at 50° C the 1-nitronaphthalene
Structure, properties, spectra, suppliers and links for: N-Phenyl-1-naphthalenamine, 90-30-2.
[N-Phenyl-1-naphthylamine] [90-30-2] | や、などのページです。
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-2-naphthylamine 97% Synonym: N-(2-Naphthyl)aniline CAS Number 135-88-6. Linear Formula C 10 H 7 NHC 6 H 5. Molecular Weight 219.28 . Beilstein/REAXYS Number 2211188 . EC Number 205-223-9. MDL number MFCD00004052. PubChem Substance ID 24850714
N- Phenyl-2-naphthylamine is an eye, skin, and mucous membrane irritant. Exposure through inhalation may cause sore throat, shortness of breath, headache, nausea, dizziness, faintness, unconsciousness, bluish skin and methemoglobinemia. Previously exposed persons may experience sensitization reactions.
N-Phenyl-1-naphthylamine | C16H13N | CID 7013 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological ...
90-30-2 - XQVWYOYUZDUNRW-UHFFFAOYSA-N - N-Phenyl-1-naphthylamine - Similar structures search, synonyms, formulas, resource links, and other chemical information.
These adducts are also formed by prostaglandin H synthase (Yamazoe et al., 1985), or from the 2-imino-1-naphthoquinone intermediate (e.g. N 4-deoxyguanosin-N 2-yl)-2-amino-1,4-naphthoquinone-imine). 2-Naphthylamine was mutagenic in S. typhimurium strains TA98 and TA100 in the presence of bovine bladder cells (Hix et al., 1983). 2-Naphthylamine ...
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.
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.
Similarly, the urine of workers exposed to N-phenyl-2-naphthylamine was found to contain 2-naphthylamine, indicating that N-phenyl-2-naphthylamine is dephenylated in the human body [ref:1]. No data were available on the genetic effects of N-phenyl-2-naphthylamine in humans. It was reported not to be mutagenic to bacteria [ref: 9].
N-Phenyl-1-naphthylamine was used in a method for determination of the concentration of organolithium and organomagnesium reagents. N-Phenyl-1-naphthylamine was used as hydrophobic probe to study the phase transitions of membrane lipids in whole cells . Packaging 500 g in glass bottle Biochem/physiol Actions
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This CICAD on N-phenyl-1-naphthylamine was based principally on a review prepared by the Laboratory studies yielded half-lives for the Fraunhofer Institute for Toxicology and Aerosol photochemical degradation of N-phenyl-1-Research, Hanover, Germany, for the German Advisory naphthylamine in water of 8.4 and 5.7 min. Photolysis
2-naphthylamine did show an increased incidence of bladder tumours. ln the latter study, the men were exposed to several compounds, which probably included N-phenyl-2-naph-thylaminel. B. Evidence for carcinogenicity to animais (limited) N-Phenyl-2-naphthylamine was tested for carcinogenicity by oral administration in mice, rats, hamsters and dogs.
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
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.
An important derivative is naphthionic acid (1-aminonaphthalene-4-sulfonic acid), which produced by heating 1-naphthylamine and sulfuric acid to 170–180 °C in the presence of crystallized oxalic acid. It forms small needles, very sparingly soluble in water.
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N-Phenylnaphthalen-1-amine (NPN) is a nonpolar, hydrophobic molecule with the chemical formula C 16 NH 13.This molecule is most notable for its binding affinity in mouse major urinary protein (MUP).
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.
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Page 1 of 1 . PANA (N-Phenyl-alpha-naphthylamine) CAS No. 90-30-2 . HN. 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.
68259-36-9 - WMLKTLDRCSEWQL-UHFFFAOYSA-N - (2,4,4-Trimethylpent-2-yl)-N-phenyl-1-naphthylamine - Similar structures search, synonyms, formulas, resource links, and other chemical information.
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