Prop. 1975/76:5 - lagen.nu
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O- OR P- 4-amino-2',3-dimethylazobenzene. 4-o-tolylazo-o-toluidine. 6a. 99-55-8. 612-210-00-5. 202-765-8. 5-nitro-o-toluidine.
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nitration of toluene with a mixture of dil nitric acid and dil sulphuric acid gives a mixture of ortho and para nitro toluene which are separated by … TWA 5 ppm (30 mg/m 3 ) [skin] NIOSH XT3325000. Chemical Class: A mononitrotoluene that consists of toluene bearing a nitro substituent at the 4-position. ChEBI CHEBI:35227, https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:35227. Gas Chromatography. General description 2-Nitrotoluene is a nitroaromatic compound. Multi-functional magnetic resins having high surface area and ion exchange efficiency (GMA30-1 and GMA30-2) were developed and were tested for the desorption of 2-nitrotolene. It is well known that symmetric molecules have higher melting points than nonsymmetric ones, e.g.
av J Han · 2019 · Citerat av 6 — T(p-OCH3)PPCoCl was introduced as carriers that selectively and Pyrrole (10 mmol) dissolved in o-nitrotoluene (10 mL) was added 820212. Produktnamn.
polychlorinated phenoxyphenol — Svenska översättning
In a 5-l. round-bottomed flask, fitted with a mechanical stirrer, are placed 680 g. (2.3 moles) of sodium dichromate, 1500 cc.
Klorobensen - Svenska - Engelska Översättning och exempel
612-210-00-5. 202-765-8. 5-nitro-o-toluidine.
H 2 SO 4 /HNO 3, it results in a mix of o- and p-nitrotoluene. How can they be separated? Which product is more prevalent?
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Relative testis weights were unchanged in dosed animals. Potential treatment-related gross lesions were limited to 2 males from the 10000 ppm exposure group which had small testes.
o- and p-Nitrotoluene--The ortho- and para- isomers of nitrotoluene are widely used in production of agricultural and rubber chemicals and a variety of dyes for cotton, wool, silk, leather, and paper, o-Nitrotoluene yielded clear evidence of carcinogenic activity in all four sex/species groups, producing skin and mammary gland neoplasms in male
1. a process for the production of p-nitrotoluene-2-sulfonic acid, which comprises (a) intimately contacting molten p-nitrotoluene with a mixture of at most 50% by volume of gaseous sulfur trioxide and an inert gas at a temperature in the range of from about 90 to 150* c., the sulfur trioxide being used in about 1 to 15% molar excess over the p-nitrotoluene employed, (b) adding water to the
Process of preparing a not discolored p-nitrobenzoic acid by oxidation of p-nitrotoluene with oxygen, which comprises contacting the oxygen with the p-nitrotoluene in an acetic acid reaction medium and in the presence of a cobalt-containing and bromine-containing catalyst at a temperature of 80° to 150° C.
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Gross and histopathological examinations of the reproductive systems indicated that p-nitrotoluene might be a reproduction toxicant. Relative testis weights were unchanged in dosed animals.
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Dunnick JK(1), Elwell MR, Bucher JR. Author information: (1)National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709.