| Identification | More | [Name]
Iminodibenzyl | [CAS]
494-19-9 | [Synonyms]
10,11-DIHYDRO-5H-DIBENZ[B,F]AZEPINE
10,11-DIHYDRO-5H-DIBENZO[B,F]AZEPINE
2,2'-IMINODIBENZYL
IMIDODIBENZYL
IMINODIBENZYL
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(
f]azepine,10,11-dihydro-5h-dibenz[
Iminobibenzyl
Iminodibenzyyl
RP 23669
Iminodibenzyl,97%
5H-Dibenzb,fazepine, 10,11-dihydro-
10,11-DIHYDRO-5H-DIBENZ(B,F)AZEPINE(IMINODIBENZYL) | [EINECS(EC#)]
207-787-1 | [Molecular Formula]
C14H13N | [MDL Number]
MFCD00005070 | [Molecular Weight]
195.26 | [MOL File]
494-19-9.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36:Irritating to the eyes.
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
S39:Wear eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S27:Take off immediately all contaminated clothing . | [WGK Germany ]
3
| [RTECS ]
HN8950000
| [TSCA ]
Yes | [HazardClass ]
IRRITANT | [HS Code ]
29339930 |
| Hazard Information | Back Directory | [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. | [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 |
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