M70533
1-甲基-3-苯基丙胺
98%
别名:
3-氨基-1-苯基丁烷, 4-苯基-2-丁胺
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关于此项目
线性分子式:
C6H5CH2CH2CH(NH2)CH3
CAS Number:
分子量:
149.23
Beilstein:
2413110
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
描述
Drug Control: Pszichotróp anyag / Psychotropic Substance (Hungary), 78/2022. (XII. 28.) BM rendelet
质量水平
方案
98%
表单
liquid
drug control
Pszichotróp anyag / Psychotropic Substance (Hungary), 78/2022. (XII. 28.) BM rendelet
折射率
n20/D 1.514 (lit.)
沸点
228-232 °C (lit.)
密度
0.922 g/mL at 25 °C (lit.)
SMILES字符串
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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警示用语：
Danger
危险分类
Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B
储存分类代码
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 2
闪点(°F)
208.0 °F
闪点(°C)
97.78 °C
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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
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
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
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