103-03-7NC(=O)NNc1ccccc1AVKHCKXGKPAGEI-UHFFFAOYSA-N103-03-7DTXSID9020245CHEMBL1593719CHEBI:82521Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.
Warning
H302 (88.9%): Harmful if swallowed [Warning Acute toxicity, oral];H315 (15.6%): Causes skin irritation [Warning Skin corrosion/irritation];H319 (15.6%): Causes serious eye irritation [Warning Serious eye damage/eye irritation];H335 (13.3%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation];H351 (13.3%): Suspected of causing cancer [Warning Carcinogenicity]
P203, P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P318, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 45 reports by companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.;Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.
Phenicarbazide
Group 3: Not classifiable as to its carcinogenicity to humans
Volume 12: (1976) Some Carbamates, Thiocarbamates and Carbazides;Volume Sup 7: Overall Evaluations of Carcinogenicity: An Updating of IARC Monographs Volumes 1 to 42, 1987; 440 pages; ISBN 92-832-1411-0 (out of print)
Beschreibung1-Phenylsemicarbazid bildet farblose, in kaltem Wasser schwer lösliche Blättchen. Leicht löslich ist es in heißem Wasser sowie Ethanol und Aceton. Die Susbtanz besitzt stark antipyretische Wirkung und wurde früher Tuberkulose-Patienten gegen Fieber in Dos
Verwenden1-Phenylsemicarbazide was used in the synthesis of a series of alkyl(aryl/heteroaryl) substituted 3-trifluoromethyl-1H-1-phenylpyrazoles and alkyl 3-carboxylate analogs by the cyclocondensation reactions with 4-alkoxy-1,1,1-trihaloalk-3-en-2-ones.
Wird geladen…
1987
1987