Melting point	182-192 ºC
Specific optical rotation	-16.5 º (c=2, H2O)
Water Solubility	soluble

SDS/MSDS	S24/25

Source	SDS/MSDS Samples
没有数据	没有数据

Synthetic Route

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Name	CAS

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Articles

Peer-Reviewed Papers

Development of "Quick-DB forensic": A total workflow from QuEChERS-dSPE method to GC-MS/MS quantification of forensically relevant drugs and pesticides in whole blood.Maiko Kusano et al.Forensic science international, 300, 125-135 (2019-05-20) Labetalol is metabolized oxidatively in humans.J Gal et al.Research communications in chemical pathology and pharmacology, 62(1), 3-17 (1988-10-01) Identification and quantitation of an oxidative metabolite of labetalol in sheep: pharmacokinetic and metabolic implications.K Yeleswaram et al.Biological mass spectrometry, 21(11), 534-540 (1992-11-01) A labetalol metabolite with analytical characteristics resembling amphetamines.R B Gilbert et al.Journal of analytical toxicology, 19(2), 84-86 (1995-03-01) Disposition, metabolism, and pharmacodynamics of labetalol in adult sheep.K Yeleswaram et al.Drug metabolism and disposition: the biological fate of chemicals, 21(2), 284-292 (1993-03-01) Quantification of Methylphenidate, Dexamphetamine, and Atomoxetine in Human Serum and Oral Fluid by HPLC With Fluorescence Detection.Benedikt Stegmann et al.Therapeutic drug monitoring, 38(1), 98-107 (2015-09-09) Upgraded Bioelectrocatalytic N2 Fixation: From N2 to Chiral Amine Intermediates.Hui Chen et al.Journal of the American Chemical Society, 141(12), 4963-4971 (2019-03-06) Stereospecific gas chromatographic/mass spectrometric assay of the chiral labetalol metabolite 3-amino-1-phenylbutane.A Changchit et al.Biological mass spectrometry, 20(12), 751-758 (1991-12-01)

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