Detail of > 83-07-8
- CAS Number:
- 83-07-8
- Name:
3H-Pyrazol-3-one,4-amino-1,2-dihydro-1,5-dimethyl-2-phenyl-
- Superlist Name:
- 4-Aminoantipyrine
- Formula:
- C11H13N3O
- Molecular Structure:

- Synonyms:
- Antipyrine,4-amino- (8CI);1,2-Dihydro-1,5-dimethyl-2-phenyl-4-amino-3H-pyrazol-3-one;4-AAP;4-Amino-1,5-dimethyl-2-phenyl-1,2-dihydro-3H-pyrazol-3-one;4-Amino-1,5-dimethyl-2-phenylpyrazolin-3-one;4-Amino-2,3-dimethyl-1-phenyl-5-pyrazolone;Aminoantipyrine;Ampyrone;NSC 60242;1-Phenyl-2,3-dimethyl-4-aminopyrazol-5-one;
- Molecular Weight:
- 203.24
- EINECS:
- 201-452-3
- Density:
- 1.207 g/cm3
- Melting Point:
- 105-110 °C(lit.)
- Boiling Point:
- 309 °C at 760 mmHg
- Flash Point:
- 140.7 °C
- Solubility:
- water: 0.1 g/mL, clear
- Appearance:
- Amber crystalline powder
- Hazard Symbols:
Xn- Risk Codes:
- 22-36/37/38-20/21/22
- Safety:
- 26-36-36/37/39Details
- particular:
- particular
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Reference
- Interactions of aminophenazone, nicotinamide, 4-aminoantipyrine and sodium p-aminosalicylate with pectic acid
- Interactions of aminophenazone, nicotinamide, 4-aminoantipyrine and sodium p-aminosalicylate with pectic acid. Mitterhauszerova, L.; Kralova, K.; Krasnec, L. (Chem. Ustav, Univ. Komenskeho, Bratislava, Czech.). Farm. Obz., 52(11), 501-8 (Slovak) 1983. CODEN: FAOBAS. ISSN: 0014-8172. DOCUMENT TYPE: Journal CA Section: 63 (Pharmaceuticals) The interaction of aminophenazone (I) [58-15-1], nicotinamide (II) [98-92-0], 4-aminoantipyrine (III) [83-07-8], and Na p-aminosalicylate (IV) [133-10-8] with citrus pectin [9000-69-5] and pectin hydrolyzed to varying degrees of esterification was studied to evaluate possible use of pectins as adjuvants in controlled-release formulations. The degree of pectin esterification was neg. correlated with the no. of binding sites for the drugs; assocn. consts. were not affected by the degree of esterification. Assocn. consts. for the drugs followed the order I > IV > III > II; the no. of binding sites followed the order I > III > II = IV. The no. of binding sites was lower than the no. of free CO2H groups. Apparently, factors other than acid-base interactions are involved in detg. binding sites.
- Colorimetric determination and stability of sodium novaminesulfonate in solutions
- Colorimetric determination and stability of sodium novaminesulfonate in solutions. Altinkurt, Turan (Fac. Pharm., Univ. Hacettepe, Ankara, Turk.). Eczacilik Bul., 18(3), 42-8 (English) 1976. CODEN: ECBUAN. DOCUMENT TYPE: Journal CA Section: 64 (Pharmaceutical Analysis) Section cross-reference(s): 63 Na novaminesulfonate (I) [68-89-3] was sepd. by thin-layer chromatog. on microcryst. cellulose plates using a benzene-Et2NH solvent, scraped from the plates, and detd. colorimetrically at 474 nm. At a concn. of 100 .mu.Several substances with their cas registry numbers 58-15-1 and 519-98-2 may be metioned in this study.g I was detd. with a std. deviation of .+-.0.00175. I loss from 4 com. products, as calcd. by the above method, ranged from 8-17%. I degrdn. products in the com. samples were 4-aminophenazone [83-07-8], 4-dimethylaminophenazone [58-15-1], and 4-methylaminophenazone [519-98-2]. .
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