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M70533

Sigma-Aldrich

1-Methyl-3-phenylpropylamine

98%

Sinônimo(s):

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

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About This Item

Fórmula linear:
C6H5CH2CH2CH(NH2)CH3
Número CAS:
Peso molecular:
149.23
Beilstein:
2413110
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22

Ensaio

98%

forma

liquid

índice de refração

n20/D 1.514 (lit.)

pb

228-232 °C (lit.)

densidade

0.922 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

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

chave InChI

WECUIGDEWBNQJJ-UHFFFAOYSA-N

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Categorias relacionadas

Pictogramas

Skull and crossbonesCorrosion

Palavra indicadora

Danger

Frases de perigo

Classificações de perigo

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

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

208.0 °F

Ponto de fulgor (°C)

97.78 °C

Equipamento de proteção individual

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


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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
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
K Yeleswaram et al.
Biological mass spectrometry, 21(11), 534-540 (1992-11-01)
A sensitive and selective assay has been developed for the identification and quantitation of 3-amino-1-phenyl butane (3-APB), a metabolite of labetalol, in biological fluids using electron impact gas chromatography/mass-selective detection. Samples were extracted with n-hexane, derivatized with heptafluorobutyric anhydride and
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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