32113-41-0 Usage
Description
Acetaminophen sulfate is an inactive metabolite of the antipyretic and analgesic agent acetaminophen . It is formed from acetaminophen via the sulfotransferase (SULT) isoforms SULT2A1, SULT1E1, SULT1A1, SULT1A3, and SULT1A4.
Chemical Properties
Light-Tan Solid
Uses
Different sources of media describe the Uses of 32113-41-0 differently. You can refer to the following data:
1. A metabolite of Acetaminophen
2. A metabolite of 4-Acetaminophen (Paracetamol) as blood platelet aggregation inhibitor.
3. Paracetamol sulfate potassium salt has been used as a standard for HPLC assays of acetaminophen.
General Description
Paracetamol is an aminophenol derivative. It functions as an analgesic and antipyretic drug, which has weak inflammatory effect. Paracetamol is used to treat pyrexia and mild to moderate pain. It might inhibit atherosclerosis through its antioxidant activity.
Biochem/physiol Actions
Phase II metabolite of paracetamol.
Check Digit Verification of cas no
The CAS Registry Mumber 32113-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,1,1 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 32113-41:
(7*3)+(6*2)+(5*1)+(4*1)+(3*3)+(2*4)+(1*1)=60
60 % 10 = 0
So 32113-41-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO5S.K/c1-6(10)9-7-2-4-8(5-3-7)14-15(11,12)13;/h2-5H,1H3,(H,9,10)(H,11,12,13);/q;+1/p-1/rC8H8KNO5S/c1-6(11)10-7-2-4-8(5-3-7)14-16(12,13)15-9/h2-5H,1H3,(H,10,11)
32113-41-0Relevant articles and documents
Ground state structures of sulfate monoesters and sulfamates reveal similar reaction coordinates for sulfuryl and sulfamyl transfer
Denehy, Emma,White, Jonathan M.,Williams, Spencer J.
, p. 314 - 316 (2008/02/08)
Structure/reactivity and structure/structure correlations of 5 sulfate monoesters and 11 sulfamate esters determined by low temperature X-ray crystallography reveal similar ground state deformations that suggest similar reaction coordinates for sulfuryl and sulfamyl group transfer. The Royal Society of Chemistry 2006.