ChemSpider 2D Image | KR7000000 | C17H22ClNO

KR7000000

  • Molecular FormulaC17H22ClNO
  • Average mass291.816 Da
  • Monoisotopic mass291.138977 Da
  • ChemSpider ID8632

More details:

Validated by Experts, Validated by Users, Non-Validated, Removed by Users

[2-(diphenylmethoxy)ethyl]dimethylamine hydrochloride
147-24-0 [RN]
2-(Benzhydryloxy)-N,N-dimethylethylamine, hydrochloride
2-(diphénylméthoxy)-N,N-diméthyléthanamine chlorhydrate
2-(Diphenylmethoxy)-N,N-dimethylethanamine hydrochloride
2-(Diphenylmethoxy)-N,N-dimethylethanamine hydrochloride (1:1) [ACD/IUPAC Name]
2-(Diphénylméthoxy)-N,N-diméthyléthanamine, chlorhydrate (1:1) [French] [ACD/IUPAC Name]
2-(Diphenylmethoxy)-N,N-dimethylethanaminhydrochlorid
2-(Diphenylmethoxy)-N,N-dimethylethanaminhydrochlorid (1:1) [German] [ACD/IUPAC Name]
200-659-6 [EINECS]
More...

Validated by Experts, Validated by Users, Non-Validated, Removed by Users

DRG 0273 [DBID]
TC2D6JAD40 [DBID]
3918132 [DBID]
CCRIS 2383 [DBID]
D00669 [DBID]
D3630_SIGMA [DBID]
D7774_SIGMA [DBID]
DRG-0273 [DBID]
EU-0100377 [DBID]
MLS000028428 [DBID]
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  • Experimental Physico-chemical Properties
  • Predicted Physico-chemical Properties
  • Miscellaneous

    • Appearance:

      white crystalline powder OU Chemical Safety Data (No longer updated) More details

    • Stability:

      Stable, but slowly darkens upon exposure to light. Incompatible withstrong oxidizing agents. OU Chemical Safety Data (No longer updated) More details

    • Toxicity:

      ORL-RAT LD50 500 mg kg-1, IVN-RAT LD50 35 mg kg-1, ORL-MUS LD50 114 mg kg-1, IPR-MAM LD50 80 mg kg-1 OU Chemical Safety Data (No longer updated) More details

    • Safety:

      20-26-36/37-45-60 Alfa Aesar A10136
      25-36/37/38-40-63 Alfa Aesar A10136
      6.1 Alfa Aesar A10136
      H351-H361-H302-H315-H319-H335 Alfa Aesar A10136
      P261-P280-P281-P305+P351+P338-P405-P501a Alfa Aesar A10136
      Safety glasses, good ventilation, gloves. OU Chemical Safety Data (No longer updated) More details
      Warning Alfa Aesar A10136

    • Target Organs:

      Histamine Receptor TargetMol T0330

    • Chemical Class:

      The hydrochloride salt of diphenhydramine. ChEBI https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:4637, CHEBI:4637

    • Bio Activity:

      <p>Histamine H<sub>1</sub> antagonist. Potently activates the modified hM4Di "GRANPA" (G protein Receptor Activated by Non-Presciption Agents) DREADD receptor in vitro and in vivo.</p> Hello Bio HB2617
      7-TM Receptors Tocris Bioscience 3072
      Diphenhydramine HCl (Benadryl), a histamine H1 antagonist used as an antiemetic, antitussive, for dermatoses and pruritus, for hypersensitivity reactions, as a hypnotic, an antiparkinson, and as an in gredient in common cold preparations. MedChem Express
      Diphenhydramine HCl (Benadryl), a histamine H1 antagonist used as an antiemetic, antitussive, for dermatoses and pruritus, for hypersensitivity reactions, as a hypnotic, an antiparkinson, and as an ingredient in common cold preparations.; Target: Histamine H1 receptor; Diphenhydramine HCl (Benadryl), a histamine H1 antagonist used as an antiemetic, antitussive, for dermatoses and pruritus, for hypersensitivity reactions, as a hypnotic, an antiparkinson, and as an ingredient in common cold preparations. MedChem Express HY-B0303A
      Diphenhydramine HCl (Benadryl), a histamine H1 antagonist used as an antiemetic, antitussive, for dermatoses and pruritus, for hypersensitivity reactions, as a hypnotic, an antiparkinson, and as an ingredient in common cold preparations.;Target: Histamine H1 receptorDiphenhydramine HCl (Benadryl), a histamine H1 antagonist used as an antiemetic, antitussive, for dermatoses and pruritus, for hypersensitivity reactions, as a hypnotic, an antiparkinson, and as an ingredient in common cold preparations. It has some undesired antimuscarinic and sedative effects. Diphenhydramine competes with free histamine for binding at HA-receptor sites. This antagonizes the effects of histamine on HA-receptors, leading to a reduction of the negative symptoms brought on by histamine HA-receptor binding. MedChem Express HY-B0303A
      GPCR/G protein MedChem Express HY-B0303A
      GPCR/G protein; MedChem Express HY-B0303A
      H1 receptor antagonist Tocris Bioscience 3072
      H1 receptor antagonist. Antihistamine. Tocris Bioscience 3072
      Histamine H1 receptor TargetMol T0330
      Histamine H1 Receptors Tocris Bioscience 3072
      Histamine Receptor MedChem Express HY-B0303A
      Histamine Receptors Tocris Bioscience 3072
      Neuroscience TargetMol T0330

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module, version: 14.00

No predicted properties have been calculated for this compound.

Click to predict properties on the Chemicalize site


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