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Detail of "134-91-8"

  • CAS Number:
  • 134-91-8
  • Name:
  • Benzenemethanol,4-(diethylamino)-a-[4-(diethylamino)phenyl]-

  • Molecular Structure:
  • Formula:
  • C21H30 N2 O
  • Molecular Weight:
  • 326.48
  • Synonyms:
  • Benzhydrol,4,4'-bis(diethylamino)- (6CI,8CI); 4,4'-Bis(diethylamino)benzhydrol;Bis(4-diethylaminophenyl)methanol
  • EINECS:
  • 205-162-8
  • Density:
  • 1.056 g/cm3
  • Melting Point:
  • 82°C
  • Boiling Point:
  • 492 °C at 760 mmHg
  • Flash Point:
  • 239.5 °C
  • Appearance:
  • Off-white crystalline powder
  • Risk Codes:
  • 36/37/38
  • Safety:
  • 26-36/37/39 Details

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CAS No.134-91-8 BIS(4-DIETHYLAMINOPHENYL)METHANOL

BIS(6-DIETHYLAMINOPHENYL)METHANOL

Supplier:Fine & Performance Chemicals Ltd [ United Kingdom]

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Reference

Oxime ethers of 4,4'-bis(N,N-diethylamino)benzhydrol and pressure-sensitive recording systems containing them
Oxime ethers of 4,4'-bis(N,N-diethylamino)benzhydrol and pressure-sensitive recording systems containing them. Cesark, Frank F.; Thomas, Daniel W. (American Cyanamid Co., USA). U. 83757-35-1 which is the cas registry number of one of substances is just one of reagents here.S. US 4435002 A 6 Mar 1984, 4 pp. Division of U.S. 4,351,956. (English). (United States of America). CODEN: USXXAM. CLASS: IC: B41M005-22. NCL: 282027500. APPLICATION: US 82-386561 9 Jun 1982. PRIORITY: US 81-297802 31 Aug 1981. DOCUMENT TYPE: Patent CA Section: 41 (Dyes, Organic Pigments, Fluorescent Brighteners, and Photographic Sensitizers) Section cross-reference(s): 43 Title compds. (I; R, R1 = C1-4 alkyl) are color formers exhibiting good color intensity, good sublimation resistance, and good soly. in petroleum distillate solvents. Thus, I (R = R1 = Me) [83757-32-8], prepd. by reaction of (4-Et2NC6H4)2CHOH [134-91-8] with Me2C:NOH [127-06-0] in refluxing MEK-hexane contg. MeSO3H, was sol. at 4% in kerosine and showed image color intensity 1.35 (Crystal Violet = 1.0) and only a trace of sublimation (ghosting) (16 h at 145-150 °F) when treated on color former paper. Analogs of I with Me2N instead of Et2N groups and/or with R and R1 other than C1-4 alkyl exhibited lower intensity, moderate sublimation, and/or insoly. in kerosine. .
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