As lacking of relevant impurities, those drugs quality control are limited
Overview Substance Hierarchy Chemical Structure Chemical Moieties 1 Names and Synonyms 7 Codes - Identifiers 3 Relationships: Impurities 5 References 9 Audit Information ERYTHROMYCIN F NM325T380N Overview Substance Hierarchy Chemical Structure Chemical Moieties 1 Names and Synonyms 7 Codes - Identifiers 5 Relationships: Impurities 4 References 12 Audit Information ERYTHROMYCIN E 39V2DI8XOX Formation and isolation of the impurity Erythromycin A 9-oxime has been prepared from the reaction of erythromycin-A with hydroxylamine in methanol [11, 12]
Column temperature, which has beneficial effect on resolution and peak shape (in a range of 30 - 65°C) was chosen at 65°C for the required The pharmacopoeia-registered structure-unknown impurity P in azithromycin product was purified
The impurity VII is produced when Erythromycin C undergoes the same modifications as erythromycin A
: 3225-82-9 Purity: > 95% CAT: B2694-471158 PRICE INQUIRY Custom synthesis 14-Hydroxyclarithromycin CAS No
1 Computed Properties
Computed by PubChem 2
LOTUS - the natural products occurrence database A bacteriostatic antibiotic macrolide produced by Streptomyces erythreus
14) Dates
Cas No: 114-07-8
CAT No: ALL-E04253; CAS No : 105882-69-7; Molecular Formula: C37H65NO12 ; Molecular Weight : 715
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To reflect the evolving and This page contains information about Erythromycin EP Impurity F
Method validation results have proven the method to be specific, linear precise, accurate, and robust
(Eg
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The method uses a μBondapak C 18 reversed-phase column with a mobile phase composed of acetonitrile—methanol—0
CAS 616234-56-1,733
Molecular Weight 717
Identification of impurities in erythromycin by liquid chromatography-mass spectrometric detection Satish Kumar Chitneni, Cindy Govaerts, Erwin Adams ∗ , Ann V an Schepdael, Jos Hoogmartens CAS No 546-57-6 Mol
Several manufacturing impurities may also be present, including Anant Pharmaceuticals Pvt
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Home / Erythromycin Impurities / 33396-29-1: Erythromycin EP Impurity E
Catalogue No
Erythromycin A is an important antibiotic widely used in clinical medicine against infections caused by Gram-positive bacteria, and it is the main treatment for many pulmonary infections such as Legionnaire's disease
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Run time: 5 times the retention time of erythromycin A
This page contains information about Erythromycin EP Impurity B
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) liquid chromatographic (LC) method
C37 H67 N O13
CAS NA,848
This page contains information about Erythromycin EP Impurity A
Pharmaceutical API Impurity Reference Standard Suppliers India Sales and Marketing : For Domestic : +91 8550986868 - For International Sales and Marketing : +91 8551986868 Sales : sales@anantlabs
doi: 10
Limits: — correction factors: for the calculation of contents, The preparation method of the erythromycin impurity D comprises the following steps: (1) weighing 5g of erythromycin, adding 125mL of water, slowly dropwise adding concentrated hydrochloric acid while stirring at room temperature, keeping the pH of the reaction solution at 1
It exhibits bacteriostatic action by inhibiting the growth of bacteria
Erythromycin derivatives have been used as antibacterial drugs in clinic for many years
Erythromycin is a complex macrolide antibiotic
Product ion spectra (MS/MS) of novel erythromycin impurities, the result of isolation and collisional activation in the ion trap of the precursor ions with
Review the potential adverse events associated with
Nineteen impurities in roxithromycin drug substance made in China were separated and identified by HPLC–MS n (TOF and TRAP) for the further
Impurity Q is erythromycin-6,9-imino-ether, which is an intermediate in the synthesis of azithromycin
Warnings Before taking Dosage Side effects Interactions FAQ What is erythromycin? Erythromycin belongs to a group of drugs called macrolide antibiotics
14) Dates
reported 2 impurities (impurities 1 and 2) in erythromycin-6,9-imino-ether product which is an intermediate in the synthesis of azithromycin and 2 impurities (impurities 3 and 4) in This page contains information about Erythromycin EP Impurity F
Method validation results have proven the method to be specific, linear precise, accurate, and robust
(Eg
In addition to the synthesis, characterization of these seven impurities A selective reversed phase liquid chromatography/mass spectrometry (LC/MS(n)) method is described for the identification of erythromycin impurities and related substances in commercial erythromycin samples
2004
The method uses a μBondapak C 18 reversed-phase column with a mobile phase composed of acetonitrile—methanol—0
Catalogue No
Identification of impurities in erythromycin by liquid chromatography–mass spectrometric detection Satish Kumar Chitneni, Cindy Govaerts, Erwin Adams ∗ , Ann V an Schepdael, Jos Hoogmartens CAS No 546-57-6 Mol
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