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2804-05-9

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2804-05-9 Usage

Uses

Metabolite of Azaperone (A802200), Sedative; tranquilizer.

Check Digit Verification of cas no

The CAS Registry Mumber 2804-05-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,0 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2804-05:
(6*2)+(5*8)+(4*0)+(3*4)+(2*0)+(1*5)=69
69 % 10 = 9
So 2804-05-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H24FN3O/c20-17-8-6-16(7-9-17)18(24)4-3-11-22-12-14-23(15-13-22)19-5-1-2-10-21-19/h1-2,5-10,18,24H,3-4,11-15H2

2804-05-9 Well-known Company Product Price

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  • Sigma-Aldrich

  • (32738)  Azaperol  VETRANAL, analytical standard

  • 2804-05-9

  • 32738-10MG

  • 870.48CNY

  • Detail

2804-05-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-fluorophenyl)-4-(4-pyridin-2-ylpiperazin-1-yl)butan-1-ol

1.2 Other means of identification

Product number -
Other names 1-(4-Fluorphenyl)-4-<4-(2-pyridyl)piperazino>butan-1-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2804-05-9 SDS

2804-05-9Upstream product

2804-05-9Downstream Products

2804-05-9Relevant articles and documents

Identification of metabolites of azaperone in horse urine

Sams, Richard A.,Gerken, Diane F.,Detra, Randall L.,Stanley, Scott D.,Wood, William E.,Tobin, Thomas,Yang, Jyan-Ming,Tai, Hsin-Hsinng,Jegananthan, Alwarsamy,Watt, David S.

, p. 79 - 84 (2007/10/03)

Two metabolites of the tranquilizer azaperone were extracted from alkalinized horse urine after treatment with β-glucuronidase/sulfatase from limpets (Patella vulgata). The metabolites were identified by a combination of independent chemical synthesis and GC/MS and 1H NMR analysis. The metabolites were identified as 1-(fluorophenyl)-4-[4-(5-hydroxy-2-pyridinyl)- 1-piperazinyl]-1-butanol, designated as 5'-hydroxyazaperol, and 1- (fluorophenyl)-4-[4-(5-hydroxy-2-pyridinyl)-1-piperazinyl]-1-butanone, designated as 5'-hydroxyazaperone. A TLC screening test was developed for detecting both metabolites in basic extracts of horse urine treated with β- glucuronidase/sulfatase. The screening test was used to detect azaperone metabolites in extracts of horse urine collected for 24 h alter intravenous administration of azaperone. The administration of azaperone to horses was confirmed by GC/MS identification of 5'-hydroxyazaperone and 5'- hydroxyazaperol from basic extracts of horse urine treated with β- glucuronidase/sulfatase. The extracted metabolites were treated with bis(trimethylsilyl)acetamide to produce trimethylsilyl (TMS) ether derivatives, and mass spectra and retention times were compared to those of the synthesized metabolites treated in the same manner.

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