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M70533

Sigma-Aldrich

1-Methyl-3-phenylpropylamine

98%

Synonym(s):

3-Amino-1-phenylbutane, 4-Phenyl-2-butylamine

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About This Item

Linear Formula:
C6H5CH2CH2CH(NH2)CH3
CAS Number:
22374-89-6
Molecular Weight:
149.23
Beilstein/REAXYS Number:
2413110
EC Number:
244-942-2
MDL number:
MFCD00008090
UNSPSC Code:
12352100
PubChem Substance ID:
24897138
NACRES:
NA.22

Quality Level

100

assay

98%

form

liquid

refractive index

n20/D 1.514 (lit.)

bp

228-232 °C (lit.)

density

0.922 g/mL at 25 °C (lit.)

SMILES string

CC(N)CCc1ccccc1

InChI

1S/C10H15N/c1-9(11)7-8-10-5-3-2-4-6-10/h2-6,9H,7-8,11H2,1H3

InChI key

WECUIGDEWBNQJJ-UHFFFAOYSA-N

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pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 2

flash_point_f

208.0 °F

flash_point_c

97.78 °C

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK8616
BCCH6346
BCCF7914
BCCC2580
BCBZ9660

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Fluoxetine Related Compound B United States Pharmacopeia (USP) Reference Standard

USP

1279826

Fluoxetine Related Compound B

3,3-Diphenylpropylamine 97%

Sigma-Aldrich

136298

3,3-Diphenylpropylamine

R B Gilbert et al.
Journal of analytical toxicology, 19(2), 84-86 (1995-03-01)
A metabolite of labetalol that is responsible for previous reports of false-positive assays for amphetamines by thin-layer chromatography and immunoassay has been identified. The compound, 3-amino-1-phenylbutane (APB), an oxidative metabolite of labetalol, was initially identified in a patient's urine by
K Yeleswaram et al.
Drug metabolism and disposition: the biological fate of chemicals, 21(2), 284-292 (1993-03-01)
Labetalol causes significant maternal and fetal metabolic effects in pregnant sheep (Yeleswaram et al., J. Pharmacol. Exp. Ther. 262, 683-691 (1992)). This study was undertaken to investigate the contribution of skeletal muscles in the development of metabolic acidosis induced by
Hui Chen et al.
Journal of the American Chemical Society, 141(12), 4963-4971 (2019-03-06)
Enantiomerically pure chiral amines are of increasing value in the preparation of bioactive compounds, pharmaceuticals, and agrochemicals. ω-Transaminase (ω-TA) is an ideal catalyst for asymmetric amination because of its excellent enantioselectivity and wide substrate scope. To shift the equilibrium of
J Gal et al.
Research communications in chemical pathology and pharmacology, 62(1), 3-17 (1988-10-01)
Previous studies on the metabolic fate of antihypertensive agent labetalol in humans identified only conjugated metabolites of the drug and accounted for only a portion of the dose. In this study, urine samples obtained from three patients on chronic labetalol
Maiko Kusano et al.
Forensic science international, 300, 125-135 (2019-05-20)
Trends in forensic toxicology show the advancement of rapid and sensitive analytical methods for qualitative and quantitative analysis of drugs of abuse. However, forensic toxicologists are continuously faced with the challenges of identifying and quantifying drug blood concentration while simultaneously
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