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136298

Sigma-Aldrich

3,3-Diphenylpropylamine

97%

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About This Item

Fórmula lineal:
(C6H5)2CHCH2CH2NH2
Número de CAS:
5586-73-2
Peso molecular:
211.30
EC Number:
226-984-3
MDL number:
MFCD00008202
UNSPSC Code:
12352100
PubChem Substance ID:
24848275
NACRES:
NA.22

assay

97%

refractive index

n20/D 1.583 (lit.)

mp

29-31 °C (lit.)

functional group

amine

SMILES string

NCCC(c1ccccc1)c2ccccc2

InChI

1S/C15H17N/c16-12-11-15(13-7-3-1-4-8-13)14-9-5-2-6-10-14/h1-10,15H,11-12,16H2

Inchi Key

KISZTEOELCMZPY-UHFFFAOYSA-N

Application

3,3-Diphenylpropylamine was used as internal standard for simultaneous determination of D- and L-modafinil in human plasma using stereospecific high-performance liquid chromatographic method. It was used as starting reagent in the synthesis of 3,3-diphenylpropylisocyanate.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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B Elsenhans et al.
Biochimica et biophysica acta, 813(1), 25-32 (1985-02-28)
Cationic, lipid-soluble organic compounds may interfere with cation-mediated membrane transport processes. Thus, small intestinal absorption may be influenced by lipophilic organic cations. Therefore a series of arylalkylamines was studied in the concentration range from 0.5 to 20 mmol/l for their
A L Mueller et al.
Annals of the New York Academy of Sciences, 890, 450-457 (2000-02-11)
NPS 1506 is a moderate affinity, uncompetitive N-methyl-D-aspartate (NMDA) receptor antagonist. NPS 1506 is neuroprotective in rodent models of ischemic stroke, hemorrhagic stroke, and head trauma, with a 2-hr window of opportunity. Neuroprotectant doses of NPS 1506 ranged from approximately
Shiv K Sharma et al.
Journal of medicinal chemistry, 53(14), 5197-5212 (2010-06-24)
The recently discovered enzyme lysine-specific demethylase 1 (LSD1) plays an important role in the epigenetic control of gene expression, and aberrant gene silencing secondary to LSD1 overexpression is thought to contribute to the development of cancer. We recently reported a
S H Gorman
Journal of chromatography. B, Biomedical sciences and applications, 730(1), 1-7 (1999-08-07)
Modafinil, DL-2-[(diphenylmethyl)sulfinyl]acetamide (Provigil), which is chiral at its sulfur atom, is a novel wake-promoting agent currently being developed as the racemate in the United States by Cephalon, Inc. In order to characterize the pharmacokinetic properties of each enantiomer, a stereospecific
T F Holzman et al.
Biochemistry, 20(19), 5524-5528 (1981-09-15)
We have found a new class of inhibitors of the bacterial bioluminescence reaction, the N,N-diphenylalkylamines and acids. We have studied the action of one of these compounds 2,2-diphenylpropylamine. The amine was competitive with the long-chain aliphatic aldehyde substrate (Ki congruent
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