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Detail of "90-94-8"

  • MSDS Download
  • CAS Number:
  • 90-94-8
  • Name:
  • Methanone,bis[4-(dimethylamino)phenyl]-

  • Superlist Name:
  • 4,4'-Bis(dimethylamino)benzophenone
  • Molecular Structure:
  • Formula:
  • C17H20N2O
  • Molecular Weight:
  • 268.39
  • Synonyms:
  • Benzophenone,4,4'-bis(dimethylamino)- (6CI,8CI);4,4'-Bis(N,N-dimethylamino)benzophenone;4,4'-Tetramethyldiaminobenzophenone;Bis(4-dimethylaminophenyl) ketone;Bis[p-(N,N-dimethylamino)phenyl] ketone;Di(p-dimethylamino)benzophenone;Michler's ketone;N,N,N',N'-Tetramethyl-4,4'-diaminobenzophenone;NSC 9602;Nisso Cure MABP;S 112;S 112 (ketone);p,p'-Bis(dimethylamino)benzophenone;p,p'-Tetramethyldiaminobenzophenone;
  • EINECS:
  • 202-027-5
  • Density:
  • 1.101 g/cm3
  • Melting Point:
  • 174 -176 °C(lit.)
  • Boiling Point:
  • 427.7 °C at 760 mmHg
  • Flash Point:
  • 183.9 °C
  • Solubility:
  • ethanol: 5 mg/mL, clear; water: 400 mg/L (20 °C)
  • Appearance:
  • white to light greenish crystals
  • Hazard Symbols:
  • ToxicT,IrritantXi
  • Risk Codes:
  • 45-41-68-36/37/38
  • Safety:
  • 53-45-36-26 Details

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CAS No.90-94-8 4,4'-Bis(dimethylamino)benzophenone

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CAS No.90-94-8 4,4'-Bis(dimethylamino)benzophenone

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CAS No.90-94-8 4,4'-Bis(dimethylamino)benzophenone

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CAS No.90-94-8 4,4'-Bis(dimethylamino)benzophenone

4,6'-BIS(DIMETHYLAMINO)BENZOPHENONE

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CAS No.90-94-8 4,4'-Bis(dimethylamino)benzophenone

4,4'-Bis(dimethylamino)benzophenone

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CAS No.90-94-8 4,4'-Bis(dimethylamino)benzophenone

4,6'-BIS(DIMETHYLAMINO)BENZOPHENONE

Supplier:Beijing Fubide Fine Chemical Co., Ltd [ China (Mainland)]

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CAS No.90-94-8 4,4'-Bis(dimethylamino)benzophenone

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Supplier:WEIFANG HAOXIN FINE CHEMICALS CO.,LTD. [ China (Mainland)]

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CAS No.90-94-8 4,4'-Bis(dimethylamino)benzophenone

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Supplier:Tianjin Youngshining Chemicals Co., Ltd. [ China (Mainland)]

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CAS No.90-94-8 4,4'-Bis(dimethylamino)benzophenone

Supplier:Suzhou Lintong Dyestuff Chemical Co., Ltd [ China (Mainland)]

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Reference

Electrically insulating composition
Electrically insulating composition. Shubin, N. E.; Nikolaev, V. M.; Gladilina, T. P.; Golub, N. F.; Plieva, A. D. (USSR ). U.S.S.R. SU 1078470 A1 7 Mar 1984 From: Otkrytiya, Izobret., Prom. Obraztsy, Tovarnye Znaki 1984, (9), 183. (Russian). (Union of Soviet Socialist Republics). CODEN: URXXAF. CLASS: IC: H01B003-40. APPLICATION: SU 82-3484013 17 Aug 1982. DOCUMENT TYPE: Patent CA Section: 38 (Plastics Fabrication and Uses) Title compn. with increased thermal cond. and improved processability contains 0.5-1.0 parts benzotriazole [95-14-7] or Michler ketone [90-94-8] and a filler consisting of 150-350 parts Si or SiC modified with 20-30 parts diallyl sebacate [3137-00-6] in addn. to 100 parts bisphenol A-based epoxy resin and 50-65 parts isomethyltetrahydrophthalic anhydride [26590-20-5].
Kinetics and efficiency of solar energy storage in the photochemical isomerization of norbornadiene to quadricyclane
Kinetics and efficiency of solar energy storage in the photochemical isomerization of norbornadiene to quadricyclane. Philippopoulos, Constantine; Marangozis, John (Lab. Chem. Process Eng., Natl. Tech. Univ. Athens, Athens, Greece). Ind. Eng. Chem. Prod. Res. Dev., 23(3), 458-66 (English) 1984. CODEN: IEPRA6. ISSN: 0196-4321. DOCUMENT TYPE: Journal CA Section: 52 (Electrochemical, Radiational, and Thermal Energy Technology) Section cross-reference(s): 22, 74 The conversion of norbornadiene [121-46-0] to quadricyclane by polychromatic radiation in a solar simulator was investigated. Parameters examd. were photosensitizers, reactant and sensitizer concns., insolation power, and temp. The rate of conversion and the efficiency of solar energy storage were measured and quant. related. The most efficient sensitizers in the order of decreasing efficiency were Michler's ketone [90-94-8], acetophenone [98-86-2], and benzophenone [119-61-9]. A mixt. of the sensitizers performed worse than the less efficient sensitizer, perhaps due to a mechanism of inter-sensitizer energy transfer. Data were obtained by exposing the system to the actual sunlight, and repeated photochem. conversion-thermal reversion cycling was made. The kinetics of the thermal reverse reaction was investigated. This information is useful for the development of a photochem. solar energy storage system.
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