Detail of "136-35-6"

CAS Number:
136-35-6
Name:
1-Triazene,1,3-diphenyl-
Molecular Structure:
Formula:
C12H11 N3
Molecular Weight:
197.26
Synonyms:
Triazene,1,3-diphenyl- (6CI,7CI,8CI); 1,3-Diphenyltriazene; Aniline, N-(phenylazo)-;Diazoaminobenzene; NSC 2077
EINECS:
205-240-1
Density:
1.07 g/cm³
Melting Point:
96 ºC
Boiling Point:
304.9 ºC at 760 mmHg
Flash Point:
138.2 ºC
Hazard Symbols:
Explodes on heating to 150C dangerous.
Safety:
Questionable carcinogen with experimental tumorigenic data. Mutation data reported. Strongly explosive when shocked or heated to 98°C. Mixture with acetic anhydride explodes when warmed. When heated to decomposition it emits toxic fumes of NO_x. Details

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Effects of diazo compounds on chromosomes and spindle: Effects of diazo compounds on chromosomes and spindle. Kundu, Devi (Dep. Bot., Univ. Calcutta, Calcutta, India). Biologia (Bratislava), 32(6), 423-30 (English) 1977. CODEN: BLOAAO. DOCUMENT TYPE: Journal CA Section: 3 (Biochemical Interactions) Exposure of Allium cepa root tips to diazoaminobenzene [136-35-6], Fast Blue Salt B [14263-94-6], Fast Dark Blue Salt [63224-47-5], Fast Violet Salt B [63313-51-9], and Variamine Blue Salt B [101-69-9] (followed by a recovery period in Knop's nutrient medium) decreased the rate of cell division, increased chromosome and mitotic abnormalities, and in some cases induced polyploidy and tumor formation. The influences of these azo compds. on plant cells were dependent on dye concn. length of treatment period, and length of recovery period.

Foaming of polyamide-6 in the anionic polymerization of caprolactam: Foaming of polyamide-6 in the anionic polymerization of caprolactam. Ciesielska, Danuta; Kelar, Krystyna (Zakl. Tworzyw Sztucznych "ERG", Politech. Poznan., Poznan, Pol.). Polimery (Warsaw), 29(8), 322-4 (Polish) 1984. CODEN: POLIA4. ISSN: 0032-2725. DOCUMENT TYPE: Journal CA Section: 37 (Plastics Manufacture and Processing) Section cross-reference(s): 35, 38 Highly homogeneous, low-d. polycaprolactam [25038-54-4] foams with high compression strength are prepd. by anionic polymn. of caprolactam in the presence of diazoaminobenzene (I) [136-35-6] or 1,6-hexamethylene diisocyanate (II) [822-06-0] foaming agent. When I (1% based on the monomer) was used as the foaming agent, the polymn. was conducted at 175 ± 5° in the presence of 0.65% Synhydride catalyst. I was added in an amt. of 8% and was used simultaneously as foaming agent and catalyst; the polymn. under these conditions was conducted at 180-190°. Foams prepd. in the presence of I had smaller pores than those prepd. in the presence of II.