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Merck

P32406

3-Phenyl-1-propylamine

98%

Synonym(s):

3-Phenylpropylamine, γ-Aminopropylbenzene

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About This Item

Linear Formula:
C6H5(CH2)3NH2
CAS Number:
2038-57-5
Molecular Weight:
135.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24897875
EC Number:
218-012-1
Beilstein/REAXYS Number:
2205526
MDL number:
MFCD00008224

Product Name

3-Phenyl-1-propylamine, 98%

SMILES string

NCCCc1ccccc1

InChI

1S/C9H13N/c10-8-4-7-9-5-2-1-3-6-9/h1-3,5-6H,4,7-8,10H2

InChI key

LYUQWQRTDLVQGA-UHFFFAOYSA-N

assay

98%

refractive index

n20/D 1.524 (lit.)

bp

221 °C (lit.)

density

0.951 g/mL at 25 °C (lit.)

Quality Level

200

Gene Information

human ... AOC3(8639)
mouse ... Aoc3(11754)

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Related Categories

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

195.8 °F - closed cup

flash_point_c

91 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK1462
BCCF8043
BCBS5399V
BCBQ6190V
BCBN4447V

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Isabella Barros Almeida et al.
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R Herráez-Hernández et al.
Journal of chromatography. B, Biomedical applications, 679(1-2), 69-78 (1996-04-26)
A method for the determination of amphetamine and related compounds in urine based on on-line derivatization with 9-fluorenylmethyl chloroformate (FMOC) and high-performance liquid chromatography is described. Derivatization is performed in a 20 x 2.1 mm I.D. column packed with a
Mohammad Darvishnejad et al.
Talanta, 199, 547-555 (2019-04-07)
In the present study, a low-cost, convenient and reliable thin film coating was developed as the extraction phase. The new sorbent was obtained by chemical bond formation between the hybrid sol-gel precursors and aluminum strip substrate in the first step
Siyu Wang et al.
Journal of agricultural and food chemistry, 65(2), 364-372 (2016-12-23)
Wolfberry or Goji berry, the fruit of Lycium barbarum, exhibits health-promoting properties that leads to an extensive study of their active components. We synthesized a set of hydroxycinnamic acid amide (HCCA) compounds, including trans-caffeic acid, trans-ferulic acid, and 3,4-dihydroxyhydrocinnamic acid
P F Fitzpatrick et al.
Archives of biochemistry and biophysics, 249(1), 70-75 (1986-08-15)
In order to determine the order of substrate binding to dopamine beta-hydroxylase during catalysis, the effect of alternate substrates upon kinetic parameters was examined. The V/K value for ascorbate was unchanged when tyramine, phenylpropylamine, p-Cl-phenethylamine, p-CH3O-phenethylamine, or phenethylamine was the
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