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N-Benzyl-1-phenoxy-d5-propan-2-amine Hydrochloride

Chemical Properties and Information

Product Code: CS-T-100778 Stable Isotopes
N-Benzyl-1-phenoxy-d5-propan-2-amine Hydrochloride
API Family
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Product Code
CS-T-100778

N-Benzyl-1-phenoxy-d5-propan-2-amine Hydrochloride

Stable Isotopes
Stock Status: : Enquire Live

CAT No.
CS-T-100778
CAS No.
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Molecular Formula
C16H15D5ClNO
Molecular Weight
282.82
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There is no hazardous surcharge associated with this product.
There is no packaging charge associated with this product.
For Research Purposes only. Not for Personal use.
All compounds supplied are strictly intended for laboratory, research, analytical, and scientific use only. They are not meant for human consumption, therapeutic use, or any form of clinical application.
CAS No.
-
Product Code
CS-T-100778
M.F.
C16H15D5ClNO
M.W.
282.82
Category
Stable Isotopes
Storage Condition
Refer MSDS for complete information.
IUPAC Name
N-Benzyl-1-phenoxy-d5-propan-2-amine Hydrochloride
References
"Knaqpp, D.R., et. al.: Drug Metab. Dispos., 4, 164 (1976); Glass, B., et al.: J. Pharm. Pharm. Sci., 9, 398 (2006); Huang, R., et al.: Chem. Res. Toxicol., 21, 659 (2008); Gohil, V., et al.: Nat. Biotechnol., 28, 249 (2010)"
Synonyms
N-Benzyl-phenoxyisopropylamine-d5 HCl; N-(1-Methyl-2-phenoxy-d5-ethyl)benzenemethanamine Hydrochloride; N-(1-Methyl-2-phenoxy-d5-ethyl)benzylamine Hydrochloride
Application Notes
"N-Benzyl-1-phenoxy-d5-propan-2-amine Hydrochloride is the labeled analogue of N-Benzyl-phenoxyisopropylamine Hydrochloride (B288780), a metabolite of phenoxybenzamine (P227990), an irreversible a-antagonist used in the treatment of hypertension, with a relatively slow onset and prolonged effect when compared to alternative a-blockers."
Hazard Compound
Refer MSDS for complete information.
Overview
"N-Benzyl-1-phenoxy-d5-propan-2-amine Hydrochloride is the labeled analogue of N-Benzyl-phenoxyisopropylamine Hydrochloride (B288780), a metabolite of phenoxybenzamine (P227990), an irreversible a-antagonist used in the treatment of hypertension, with a relatively slow onset and prolonged effect when compared to alternative a-blockers."
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