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Home > Products >  Phenothiazine

Phenothiazine CAS NO.92-84-2

  • Min.Order: 1 Kilogram
  • Payment Terms: L/C,T/T,Other
  • Product Details

Keywords

  • Phenothiazine
  • 92-84-2
  • THIODIPHENYLAMINE PHENOXUR

Quick Details

  • ProName: Phenothiazine
  • CasNo: 92-84-2
  • Molecular Formula: C12H9NS
  • Appearance: clean gray-green powder
  • Application: Phenothiazine is a relatively widely u...
  • DeliveryTime: 10days
  • PackAge: in foil bag or customized
  • Port: Tianjin xingang
  • ProductionCapacity: 10 Metric Ton/Day
  • Purity: 99%
  • Transportation: by sea
  • LimitNum: 1 Kilogram
  • Heavy metal: less than 0.4%
  • Grade: Industrial Grade

Superiority

Our company is a professional chemical raw materials manufacturer and exporter for many years in chemical market. There are more than 200 excellent staffs and four factories working for us .
Company advantage:
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4. Sample order are welcome.
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Details

Phenothiazine Chemical Properties
mp  184 °C
bp  371 °C(lit.)
density  1.362
refractive index  1.6353
Fp  202°C
Water Solubility  2 mg/L (25 ºC)
Sensitive  Light Sensitive
Merck  14,7252
BRN  143237
Stability: Stable. Combustible. Incompatible with strong oxidizing agents, strong acids. May discolour upon exposure to light.
CAS DataBase Reference 92-84-2(CAS DataBase Reference)
NIST Chemistry Reference Phenothiazine(92-84-2)
EPA Substance Registry System 10H-Phenothiazine(92-84-2)
Storage characteristics Treasury: ventilation low-temperature and dry; store and transport it separately from oxidant.
Extinguishing agent Dry powder, foam, sand.
Professional Standards TLV-TWA 5 mg / m³; STEL 10 mg / m.
Chemical Properties yellow or pale green powder
Usage A key component of antipsychotic and antihistaminic drugs.
Usage Employed in the preparation of carbazoles and piperazines,1 and charge-transfer semiconducting complexes.2
General Description Light green to steel-blue powder. Acquires a greenish-brown tint under exposure to sunlight.
Air & Water Reactions Insoluble in water.
Reactivity Profile Phenothiazine is slowly decomposed by sunlight. . Organosulfides are incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials generate heat and in many cases hydrogen gas. Many of these compounds may liberate hydrogen sulfide upon decomposition or reaction with an acid.
Fire Hazard Flash point data for Phenothiazine are not available, but Phenothiazine is probably combustible.

 

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