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Detail of "6630-99-5"

  • CAS Number:
  • 6630-99-5
  • Name:
  • 1,2,3,4-Thiatriazol-5-amine

  • Molecular Structure:
  • Formula:
  • CH2 N4 S
  • Molecular Weight:
  • 102.11
  • Synonyms:
  • 1,2,3,4-Thiatriazole,5-amino- (6CI,7CI,8CI); 5-Amino-1,2,3,4-thiatriazole; 5-Aminothiatriazole; AB44; NSC 55835
  • Density:
  • 1.677g/cm3
  • Boiling Point:
  • 239°Cat760mmHg
  • Flash Point:
  • 98.3°C
  • Safety:
  • Very unstable. Explodes weakly at 130°C. Upon decomposition it emits toxic fumes of SOx and NOx. Details

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Reference

Study of the effectiveness of 5-amino-1,2,3,4-thiatriazole as a blowing agent for SKI-3NTP rubber
Study of the effectiveness of 5-amino-1,2,3,4-thiatriazole as a blowing agent for SKI-3NTP rubber. Lyapina, T. Yu.; Blokh, G. A.; Tarkhov, G. V.; Mishina, I. M. (Khim.-Tekhnol. Inst., Dnepropetrovsk, USSR). Izv. Vyssh. Uchebn. Zaved., Khim. Khim. Tekhnol., 27(9), 1087-90 (Russian) 1984. CODEN: IVUKAR. ISSN: 0579-2991. DOCUMENT TYPE: Journal CA Section: 39 (Synthetic Elastomers and Natural Rubber) The properties of 5-amino-1,2,3,4-thiatriazole (I) [6630-99-5] blowing agent and its effect on the vulcanization of SKI-3NTP rubber were discussed. I increased the vulcanization rate and enhanced the physicomech. properties of the vulcanizates. The use of I instead of ChKhZ-5 blowing agent enhanced the tensile strength of the rubber vulcanizates without affecting their d.
Thermal properties of 5-(substituted)-amino-1,2,3,4-thiatriazoles
Thermal properties of 5-(substituted)-amino-1,2,3,4-thiatriazoles. Floch, L.; Martvon, A.; Kosik, M. (Fac. Chem. Technol., Slovak Tech. Univ., Bratislava, Czech.). J. Therm. Anal., 12(3), 407-11 (English) 1977. CODEN: JTHEA9. ISSN: 0368-4466. DOCUMENT TYPE: Journal CA Section: 22 (Physical Organic Chemistry) The thermal properties of 5-(substituted)-amino-1,2,3,4-thiatriazoles were studied using TG and DTA; the parent thiatriazole actively decompd. at its m.p. The decompn.In this experiment, several chemicals are used like 6630-99-5 was rapid and was accompanied by exothermic recombinations. The (substituted)-amino-1,2,3,4-thiatriazoles decompd. at slower rates in several steps; substituent effects are discussed. .
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