Product Detail
(+)-6-Aminopenicillanic Acid-d3
Stable Isotopes
Stock Status: Enquire
Live
For Research & Analytical Purposes. Not for Personal use.
Category
Stable Isotopes
API Family
--
Storage
Refer MSDS for complete information.
Hazard Information
Refer MSDS for complete information.
(+)-6-Aminopenicillanic Acid-d3 Product Information
(+)-6-Aminopenicillanic Acid-d3 is listed under Stable Isotopes. It is associated with and is intended for analytical research, quality control and pharmaceutical reference standard applications. The product is supplied by Clearsynth under CAT No. CS-T-101902.
Clearsynth provides this compound for research and analytical use, with product information including CAS number, molecular formula, molecular weight, stock enquiry details and supporting documentation.
Technical Data
Product Name
(+)-6-Aminopenicillanic Acid-d3
CAS No.
-
CAT No.
CS-T-101902
Molecular Formula
C8H9D3N2O3S
Molecular Weight
219.28
Category
Storage Condition
Refer MSDS for complete information.
IUPAC Name
(+)-6-Aminopenicillanic Acid-d3
Hazard Compound
Refer MSDS for complete information.
Description
Overview
"(+)-6-Aminopenicillanic Acid-d3 is the isotope labelled analog of (+)-6-Aminopenicillanic Acid. (+)-6-Aminopenicillanic Acid is the core structure in penicillins, obtained from the fermentation brew of the Penicillium mold. (+)-6-Aminopenicillanic Acid is used as the main starting block for the preparation of numerous semisynthetic penicillins."
Synonyms
"(2S,5R,6R)-6-Amino-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid-d3; 6-APA-d3; 6-APS-d3; 6ß-Aminopenicillanic acid-d3; NSC 50071-d3; [2S-(2a,5a,6ß)]-6-Amino-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid-d3"
Application Notes
"(+)-6-Aminopenicillanic Acid-d3 is the isotope labelled analog of (+)-6-Aminopenicillanic Acid. (+)-6-Aminopenicillanic Acid is the core structure in penicillins, obtained from the fermentation brew of the Penicillium mold. (+)-6-Aminopenicillanic Acid is used as the main starting block for the preparation of numerous semisynthetic penicillins."
References
"Zel'tser, I.Z. et al.: Gig. Truda Prof. Zabol., 5, 59 (1983); Hamilton-Miller, J.M.T.: Int. J. Antimicrob. Agents, 31, 189 (2008); Novikova, N.D. et al.: Mikol. Fitopatol., 7, 101 (1973);"
![D-[4-13C;4-D]ribose chemical structure](https://structures.clearsynth.com/CS-OC-00614.PNG)
