ChemicalBook >> CAS DataBase List >>N-benzyl-N-(2-chloroethyl)-1-(2,3,4,5,6-pentadeuteriophenoxy)propan-2-amine:hydrochloride

N-benzyl-N-(2-chloroethyl)-1-(2,3,4,5,6-pentadeuteriophenoxy)propan-2-amine:hydrochloride

CAS No.
1329838-45-0
Chemical Name:
N-benzyl-N-(2-chloroethyl)-1-(2,3,4,5,6-pentadeuteriophenoxy)propan-2-amine:hydrochloride
Synonyms
Phenoxybenzamine-d5 HCl;N-benzyl-N-(2-chloroethyl)-1-(2,3,4,5,6-pentadeuteriophenoxy)propan-2-amine:hydrochloride
CBNumber:
CB53394486
Molecular Formula:
C18H18Cl2D5NO
Molecular Weight:
345.31812889
MDL Number:
MFCD34568001
MOL File:
1329838-45-0.mol
MSDS File:
SDS
Last updated:2026-05-28 05:24:10

N-benzyl-N-(2-chloroethyl)-1-(2,3,4,5,6-pentadeuteriophenoxy)propan-2-amine:hydrochloride Properties

storage temp. Store at -20°C
solubility DMF: 30 mg/ml; DMF:PBS (pH 7.2) (1:1): 0.3 mg/ml; DMSO: 25 mg/ml; Ethanol: 25 mg/ml
form A solid

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)Health Hazard (GHS08)
GHS07,GHS08
Signal word  Warning
NFPA 704
0
2 0

N-benzyl-N-(2-chloroethyl)-1-(2,3,4,5,6-pentadeuteriophenoxy)propan-2-amine:hydrochloride price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 29996 Phenoxybenzamine-d5 (hydrochloride) ≥98%deuteratedforms(d1-d5) 1329838-45-0 1mg $391 2026-04-30 Buy
Cayman Chemical 29996 Phenoxybenzamine-d5 (hydrochloride) ≥98%deuteratedforms(d1-d5) 1329838-45-0 5mg $1074 2026-04-30 Buy
TRC P227992 Phenoxybenzamine-d5Hydrochloride 1329838-45-0 10mg $1230 2021-12-16 Buy
Product number Packaging Price Buy
29996 1mg $391 Buy
29996 5mg $1074 Buy
P227992 10mg $1230 Buy

N-benzyl-N-(2-chloroethyl)-1-(2,3,4,5,6-pentadeuteriophenoxy)propan-2-amine:hydrochloride Chemical Properties, Uses, Production

Description

Phenoxybenzamine-d5 is intended for use as an internal standard for the quantification of phenoxybenzamine by GC- or LC-MS. Phenoxybenzamine is an antagonist of α-adrenergic receptors (α-ARs). It inhibits norepinephrine-induced inositol phosphate formation in HEK293 cells expressing α1-ARs (EC50s = 125.9-316.2 nM), as well as radioligand binding to α2A-, α2B-, and α2C-ARs in CHO cell membranes (Kis = 60, 10, and 60 nM, respectively). Phenoxybenzamine (0.5-5 μM) decreases norepinephrine-, histamine-, and calcium-induced contractions in isolated rabbit aortic strips. It also inhibits proliferation of nine cancer cell lines, including lymphoma, breast, and lung cancer cells, with IC50 values ranging from 29.5 to 99.8 μM. Phenoxybenzamine (3-1,000 μg/kg) reduces increases in diastolic blood pressure induced by the α-AR agonists cirazoline , St-587, Sgd 101/75, and B-HT 920 in pithed rats. It also decreases the time to find the platform in the Morris water maze, indicating restored spatial memory, in a rat model of fluid percussion-induced traumatic brain injury (TBI). Formulations containing phenoxybenzamine have been used in the treatment of hypertension and hyperhidrosis associated with pheochromocytomas, an adrenal medullary neuroendocrine tumor.

Uses

An irreversible α-antagonist. Used in the treatment of hypertension, it has a relatively slow onset and prolonged effect when compared to alternative α-blockers.

References

[1] K P MINNEMAN. Selectivity of agonists for cloned alpha 1-adrenergic receptor subtypes.[J]. Molecular Pharmacology, 1994, 46 5: 929-936.
[2] H. FRANG. Phenoxybenzamine Binding Reveals the Helical Orientation of the Third Transmembrane Domain of Adrenergic Receptors*[J]. The Journal of Biological Chemistry, 2001, 29 1: 31279-31284. DOI: 10.1074/jbc.m104167200
[3] GRANT A. MCPHERSON  Errol M  Elena Krstew. EFFECTS OF PHENOXYBENZAMINE ON RESPONSES TO SOME RECEPTOR AGONISTS AND CALCIUM IN VITRO[J]. Clinical and Experimental Pharmacology and Physiology, 1985, 12 5: 455-464. DOI: 10.1111/j.1440-1681.1985.tb00895.x
[4] INCHIOSA M A. Anti-tumor activity of phenoxybenzamine and its inhibition of histone deacetylases.[J]. ACS Applied Bio Materials, 2018: e0198514. DOI: 10.1371/journal.pone.0198514
[5] P B TIMMERMANS. Effects of the irreversible alpha-adrenoceptor antagonists phenoxybenzamine and benextramine on the effectiveness of nifedipine in inhibiting alpha 1- and alpha 2-adrenoceptor mediated vasoconstriction in pithed rats.[J]. Naunyn-Schmiedeberg’s archives of pharmacology, 1985, 329 4: 404-413. DOI: 10.1007/bf00496376
[6] THOMAS F RAU. Phenoxybenzamine is neuroprotective in a rat model of severe traumatic brain injury.[J]. International Journal of Molecular Sciences, 2014, 15 1: 1402-1417. DOI: 10.3390/ijms15011402

N-benzyl-N-(2-chloroethyl)-1-(2,3,4,5,6-pentadeuteriophenoxy)propan-2-amine:hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

N-benzyl-N-(2-chloroethyl)-1-(2,3,4,5,6-pentadeuteriophenoxy)propan-2-amine:hydrochloride Suppliers

Global Suppliers ( 11)
Supplier Tel Email Country ProdList Advantage
Shanghai Hongye Biotechnology Co. Ltd 400-9205774 400-920-5774 sales@glpbio.cn China 6705 58
ChemeGen(Shanghai) Biotechnology Co.,Ltd. 18818260767 sales@chemegen.com China 11123 58
Energy Chemical 400-0056266 marketing1@energy-chemical.com China 44927 58
CHINA ISOTOPE CO., LIMITED 02151600108 13062666369 info@isotopechem.com China 4721 58
Shanghai Yifei Biotechnology Co. , Ltd. 021-65675885 18964387627 customer_service@efebio.com China 11963 58
Nanjing Shizhou Biology Technology Co.,Ltd 17301488900 judy.xia@synzest.com China 12577 58
TLC Pharmaceutical Standards Ltd. 18012923235 chinasales04@tlcstandards.com.cn China 8143 58

1329838-45-0 (N-benzyl-N-(2-chloroethyl)-1-(2,3,4,5,6-pentadeuteriophenoxy)propan-2-amine:hydrochloride) Related Search:

N-benzyl-N-(2-chloroethyl)-1-(2,3,4,5,6-pentadeuteriophenoxy)propan-2-amine:hydrochloride Phenoxybenzamine-d5 HCl 1329838-45-0