Reference Standard Product Detail

Erythromycin

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Product Code: CS-O-11641 Reference Standard Research Use Only
Erythromycin
Category
Reference Standard
API Family
Erythromycin
Product Code
CS-O-11641
Research Status
For Laboratory Use

Erythromycin

Erythromycin Reference Standard
Stock Status: In Stock
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CAT No.
CS-O-11641
CAS No.
114-07-8
Molecular Formula
C₃₇H₆₇NO₁₃
Molecular Weight
733.93
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There is no hazardous surcharge associated with this product.
There is no packaging charge associated with this product.
For Research Purposes only. Not for Personal or Veterinary use.
All compounds supplied are strictly intended for laboratory, research, analytical, and scientific use only. They are not meant for human consumption, therapeutic use, or any form of clinical application.
CAS No.
114-07-8
Product Code
CS-O-11641
M.F.
C₃₇H₆₇NO₁₃
M.W.
733.93
Smiles
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Category
Reference Standard
API Family
Erythromycin
Storage Condition
Store at refrigerator (2-8°C) for long term storage
IUPAC Name
(3R,4S,5S,6R,7R,9R,11R,12R,13S,14R)-6-(((2S,3R,4S,6R)-4-(dimethylamino)-3- hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-14-ethyl-7,12,13-trihydroxy-4- (((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)- 3,5,7,9,11,13-hexamethyloxacyclotetradecane-2,10-dione
References
Synonyms
Not available,
Application Notes
"Erythromycin is bacteriostatic antibiotic macrolide produced by Streptomyces erythreus. Erythromycin A is considered its major active component. In sensitive organisms, it inhibits protein synthesis by binding to 50S ribosomal subunits. This binding process inhibits peptidyl transferase activity and interferes with translocation of amino acids during translation and assembly of proteins." "Koch; W,L,; et al,: Anal, Profiles Drug Subs,; 8; 157 (1979);"
Purity by HPLC
Not less than 90 %
Hazard Compound
Refer MSDS for accurate information.
Overview
"Erythromycin is bacteriostatic antibiotic macrolide produced by Streptomyces erythreus. Erythromycin A is considered its major active component. In sensitive organisms, it inhibits protein synthesis by binding to 50S ribosomal subunits. This binding process inhibits peptidyl transferase activity and interferes with translocation of amino acids during translation and assembly of proteins." "Koch; W,L,; et al,: Anal, Profiles Drug Subs,; 8; 157 (1979);"

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