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105093-21-8

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105093-21-8 Usage

Chemical Properties

Off-White to Pale Beige Solid

Check Digit Verification of cas no

The CAS Registry Mumber 105093-21-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,0,9 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105093-21:
(8*1)+(7*0)+(6*5)+(5*0)+(4*9)+(3*3)+(2*2)+(1*1)=88
88 % 10 = 8
So 105093-21-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H18FN3O6S/c18-13-7-11-14(21(10-1-2-10)9-12(16(11)22)17(23)24)8-15(13)19-3-5-20(6-4-19)28(25,26)27/h7-10H,1-6H2,(H,23,24)(H,25,26,27)

105093-21-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Ciprofloxacin Piperazinyl-N4-sulfate

1.2 Other means of identification

Product number -
Other names 1-cyclopropyl-6-fluoro-4-oxo-7-(4-sulfopiperazin-1-yl)quinoline-3-carboxylic acid

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:105093-21-8 SDS

105093-21-8Upstream product

105093-21-8Downstream Products

105093-21-8Relevant articles and documents

Isolation and structural elucidation of urinary metabolites of ciprofloxacin

Gau,Kurz,Petersen,Ploschke,Wuensche

, p. 1545 - 1549 (2007/10/02)

After oral administration of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-piperazine-1-ylqu inoline-3-carboxylic acid (ciprofloxacin, Bay o 9867; designated trademark: Ciprobay) four metabolites M1-M4 were isolated from human urine by Craig counter current distribution and semipreparative high-performance liquid chromatography. Their molecular structures were elucidated by nuclear magnetic resonance and mass spectrometry and confirmed by comparing their spectra with those of authentic synthetic reference compounds.

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