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
化学文摘社编号:
分子量:
149.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
244-942-2
Beilstein/REAXYS Number:
2413110
MDL number:
产品名称
1-甲基-3-苯基丙胺, 98%
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
SMILES string
CC(N)CCc1ccccc1
description
Drug Control: Pszichotróp anyag / Psychotropic Substance (Hungary), 78/2022. (XII. 28.) BM rendelet
assay
98%
form
liquid
drug control
Pszichotróp anyag / Psychotropic Substance (Hungary), 78/2022. (XII. 28.) BM rendelet
refractive index
n20/D 1.514 (lit.)
bp
228-232 °C (lit.)
density
0.922 g/mL at 25 °C (lit.)
Quality Level
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 2
flash_point_f
208.0 °F
flash_point_c
97.78 °C
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
A Changchit et al.
Biological mass spectrometry, 20(12), 751-758 (1991-12-01)
We previously identified 3-amino-1-phenylbutane (APB) as an oxidative N-dealkylated, metabolite of the antihypertensive agent labetalol. Labetalol has two asymmetric centers and is used clinically as a mixture of the four possible stereoisomers; APB has one asymmetric center. We now report
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
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
Benedikt Stegmann et al.
Therapeutic drug monitoring, 38(1), 98-107 (2015-09-09)
For psychostimulants, a marked individual variability in the dose-response relationship and large differences in plasma concentrations after similar doses are known. Therefore, optimizing the efficacy of these drugs is at present the most promising way to exploit their full pharmacological
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
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