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| | Iminodibenzyl Basic information |
| Product Name: | Iminodibenzyl | | Synonyms: | TIMTEC-BB SBB003595;10,11-Dihydro-5-dibenz(b,f)azepine;10,11-Dihydrodibenz[b,f]azepine;2,2’-iminobibenzyl;2,2'-Iminobibenzyl;3,4-Dihydro-2.36.7-dibenzazepine;5H-Dibenzo[b,f]azepine, 10,11-dihydro-;f)azepine,10,11-dihydro-5h-dibenz( | | CAS: | 494-19-9 | | MF: | C14H13N | | MW: | 195.26 | | EINECS: | 207-787-1 | | Product Categories: | Aromatics, Enzyme substrates, Heterocycles, Metabolites & Impurities;Miscellaneous | | Mol File: | 494-19-9.mol |  |
| | Iminodibenzyl Chemical Properties |
| Melting point | 105-108 °C (lit.) | | Boiling point | 321.94°C (rough estimate) | | density | 1.0778 (rough estimate) | | refractive index | 1.6353 (estimate) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | Chloroform (Slightly), Ethyl Acetate (Slightly, Heated), Methanol (Slightly) | | pka | 0.83±0.20(Predicted) | | form | Crystalline Powder | | color | Yellow to beige | | BRN | 152732 | | LogP | 4.27 | | CAS DataBase Reference | 494-19-9(CAS DataBase Reference) | | NIST Chemistry Reference | 5H-Dibenz[b,f]azepine, 10,11-dihydro-(494-19-9) | | EPA Substance Registry System | 5H-Dibenz[b,f]azepine, 10,11-dihydro- (494-19-9) |
| | Iminodibenzyl Usage And Synthesis |
| Description | Iminodibenzyl was not a new drug. It had been discovered in 1898 and used briefly as an intermediate, in the preparation of Sky Blue, a dye stuff. Iminodibenzyl, however, had a tricyclic ring structure, similar in appearance to the phenothiazines. Iminodibenzyl is an important drug intermediate, which can be used for the medicine synthesis as a tristimania and epilepsia. | | Chemical Properties | YELLOWISH TO BEIGE CRYSTALLINE POWDER | | Uses | 10,11-Dihydro-5H-dibenzo[b,f]azepine is a metabolite of the tricyclic antidepressant, Imipramine (I465980). 10,11-Dihydro-5H-dibenzo[b,f]azepine can be used as a chromogenic probe for the quantification of hydrogen peroxide and glucose. | | Uses | These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements. | | Preparation | Iminodibenzyl is obtained from o-nitrotoluene by condensation, reduction and cyclization. | | General Description | Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards |
| | Iminodibenzyl Preparation Products And Raw materials |
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