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P32406

Sigma-Aldrich

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:
Molecular Weight:
135.21
Beilstein:
2205526
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

refractive index

n20/D 1.524 (lit.)

bp

221 °C (lit.)

density

0.951 g/mL at 25 °C (lit.)

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

Gene Information

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

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Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

195.8 °F - closed cup

Flash Point(C)

91 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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
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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
Cyntia M Palacio et al.
The FEBS journal, 286(20), 4086-4102 (2019-06-05)
The biodegradation of the nylon-6 precursor caprolactam by a strain of Pseudomonas jessenii proceeds via ATP-dependent hydrolytic ring opening to 6-aminohexanoate. This non-natural ω-amino acid is converted to 6-oxohexanoic acid by an aminotransferase (PjAT) belonging to the fold type I pyridoxal
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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