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V900534

Sigma-Aldrich

Dibenzylamine

Vetec, reagent grade, 97%

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About This Item

Linear Formula:
(C6H5CH2)2NH
CAS Number:
Molecular Weight:
197.28
Beilstein/REAXYS Number:
909664
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Pricing and availability is not currently available.

grade

reagent grade

product line

Vetec

assay

97%

refractive index

n20/D 1.574 (lit.)

bp

300 °C (lit.)

mp

−26 °C (lit.)

density

1.026 g/mL at 25 °C (lit.)

SMILES string

C(NCc1ccccc1)c2ccccc2

InChI

1S/C14H15N/c1-3-7-13(8-4-1)11-15-12-14-9-5-2-6-10-14/h1-10,15H,11-12H2

InChI key

BWLUMTFWVZZZND-UHFFFAOYSA-N

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Legal Information

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1C

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

289.4 °F - closed cup

flash_point_c

143 °C - closed cup


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B Doepner et al.
Naunyn-Schmiedeberg's archives of pharmacology, 364(1), 9-13 (2001-08-04)
Ventricular myocytes of the mouse ventricle were voltage clamped with a patch-clamp technique in the whole-cell configuration. At depolarizing voltage pulses, these myocytes develop a large voltage-dependent K+ outward current. Application of the drug dibenzylamine (DBA) to the bath solution
P Nagaraja et al.
Journal of pharmaceutical and biomedical analysis, 29(1-2), 277-282 (2002-06-14)
Novel coupling reagents are used for the sensitive spectrophotometric determination of nimesulide (NIME) in either pure form or in its pharmaceutical preparations. The methods are based on the diazotisation of reduced NIME, followed by either coupling with alcoholic iminodibenzyl (IDB)
Jong M Rho et al.
Epilepsia, 43(4), 358-361 (2002-04-16)
To investigate whether ketone bodies are directly anticonvulsant. We tested the effects of acetoacetate (ACA), acetone, and both stereoisomers, D-(-)- and L-(+), of beta-hydroxybutyrate (BHB) on sensory-evoked seizures in Frings audiogenic seizure-susceptible mice. We found that these ketone bodies, with
Federica Barbieri et al.
Investigational new drugs, 21(4), 413-420 (2003-10-31)
The development of multidrug-resistance (MDR) in neoplastic cells is often responsible for the therapy failure and poor outcome of a number of human cancers. MDR may be associated with the expression of the multidrug transporter glycoprotein p170, encoded by the
Pharmacological and biochemical properties of iminodibenzyl antipsychotic drugs including Y-516 and clocapramine.
M Mikuni et al.
Clinical neuropharmacology, 9 Suppl 4, 319-321 (1986-01-01)

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