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The present invention relates to the preparation method of high purity Erythromycin A. Wherein, the anti-microbial activity of Erythromycin A is relatively strong, and toxicity is lower, is the main anti-microbial activity composition of medical erythromycin. Traditional technique preparing Erythromycin A is at about 30 DEG C, by erythromycin intermediate salt and acetone or acetone-methanol mixed solvent, adopts ammoniacal liquor or NaOH solution to adjust pH about Again erythromycin crystal is shuffled in the purified water of 55 DEG C, take out filter crystallization obtain Erythromycin A finished product. Therefore, need badly a kind of simple and easy to do at present, and the high purity Erythromycin A preparation method that production efficiency is higher. This Erythromycin A alkali is carried out aqueous crystallization and obtains Erythromycin A by recycling again. Through two-step reaction effectively reduce or the thiocyanic acid that eliminates in Matachrom with https://www.pcmag.com some impurity such as ion, pigment, thus prepared the Erythromycin A of high purity. Further, in step 1, described alkali is selected from sodium hydroxide or potassium hydroxide.
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Macrolide antibiotics Uses. CAS No. Request For Quotation. Properties Uses Suppliers Erythromycin thiocyanate Chemical Properties,Uses,Production Macrolide antibiotics Thiocyanate thiocyanate is the thiocyanate of commonly used macrolide antibiotic erythromycin.
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Each contraindication describes a scenario in which the drug is not to be used.
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