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Detail of "98-04-4"

  • CAS Number:
  • 98-04-4
  • Name:
  • Benzenaminium,N,N,N-trimethyl-, iodide (1:1)

  • Superlist Name:
  • Phenyltrimethylammonium iodide
  • Molecular Structure:
  • Formula:
  • C9H14 N . I
  • Molecular Weight:
  • 263.14
  • Synonyms:
  • Ammonium,trimethylphenyl-, iodide (8CI); Benzenaminium, N,N,N-trimethyl-, iodide (9CI);Trimethylphenylammonium iodide (6CI); N,N,N-Trimethylanilinium iodide;N,N-Dimethylaniline methiodide; PHT; Phenyltrimethylammonium iodide;Trimethylanilinium iodide
  • EINECS:
  • 202-630-3
  • Density:
  • g/cm3
  • Melting Point:
  • 227 ºC
  • Boiling Point:
  • °Cat760mmHg
  • Flash Point:
  • °C
  • Hazard Symbols:
  • Risk Codes:
  • R36/37/38;R41   
  • Safety:
  • Poison by intraperitoneal, subcutaneous, and intravenous routes. When heated to decomposition it emits very toxic fumes of NOx, NH3, and I. See also IODIDES. Details

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CAS No.98-04-4 Phenyltrimethylammonium iodide

Assay:98%

Supplier:Hangzhou Dayangchem Co., Ltd. [ China (Mainland)]

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Address:B/2601 Fuli Building, 328# WenEr Rd. Hangzhou City 310012 China

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CAS No.98-04-4 Phenyltrimethylammonium iodide

Phenyl Trimethyl Ammonium Iodide

Supplier:Dishman Pharmaceuticals & Chemicals Co., Ltd. [ China (Mainland)]

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Tel:+86-510-85840486 13771085865

Address:rm1101, times bldg, 655#Hubing rd, wuxi, china

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CAS No.98-04-4 Phenyltrimethylammonium iodide

Supplier:RSA Corporation [ United States]

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Tel:(203) 790-8100

Address:36 Old Sherman Turnpike Danbury, Connecticut 06810

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Reference

The effect of salts and pH on the conformation of quaternary ammonium electrolytes in aqueous solution
The effect of salts and pH on the conformation of quaternary ammonium electrolytes in aqueous solution. Petrariu, Ioan; Steinbaum, Lucian; Petrariu, Pamfilia (Rom.). Rev. Chim. (Bucharest), 28(10), 932-6 (Romanian) 1977. CODEN: RCBUAU. DOCUMENT TYPE: Journal CA Section: 35 (Synthetic High Polymers) The reduced viscosity of aq. solns. of quaternary ammonium polyelectrolytes, prepd. by chloromethylation and amination of polystyrene (I), decreased with increasing concn. due to changes in the nature of bonding and increased mol. mobility. The polyelectrolytes were prepd. by chloromethylation of I, amination with (2-hydroxyethyl)dimethylamine, and, in 1 case, subsequent chlorination of the hydroxyethyl group by treatment with SOCl2. Viscosity measurements were made at 0.10-1.0% concn. in water and in NaCl, NaOH, and HCl solns. (0.005-0.1, 0.1-1.0, and 0.01-0.1N resp.) at 25, 50, and 75°. The reduced viscosity was always lower in the presence of electrolyte solns. and showed the same tendency to increase with decreasing concn., but to a lesser extent than in water. Bu4NI [311-28-4] and Me3PhNI [98-04-4] solns. were used as model compds.
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