CasNo.217500-96-4,Tulathromycin 217500-96-4 Large in promotion,(217500-96-4) Suppliers

1 Kilogram	Negotiable

Min.Order :1 Kilogram
Purity: 95%~103.0%
Payment Terms : T/T,Other

Keywords

217500-96-4 Tulathromycin Tulathromycin A

Quick Details

Appearance:white powder
Application:intermediate
PackAge:drums
ProductionCapacity:100|Kilogram|Month
Storage:dry and cool
Transportation:air, courier and sea

Superiority:

Synonyms: TULATHROMYCIN A;(2R,3S,4R,5R,8R,10R,11R,12S,13S,14R)-13-[[2,6-Dideoxy-3-C-methyl-3-O-methyl-4-C-[(propylamino)methyl]-a-L-ribo-hexopyranosyl]oxy]-2-ethyl-3,4,10-trihydroxy-3,5,8,10,12,14-hexamethyl-11-[[3,4,6-trideoxy-3-(dimethylamino)-b-D-xylo-hexopyranosyl]oxy]-1-oxa-6-azacyclopentadecan-15-one;Unii-897A3kn7ap;(2R,3S,4R,5R,8R,10R,11R,12S,13S,14R)-13-[[2,6-Dideoxy-3-C-Methyl-3-O-Methyl-4-C-[(propylaMino)Methyl]-α-L-ribo-hexopyranosyl]oxy]-2-ethyl-3,4,10-trihydroxy-3,5,8,10,12,14-hexaMethyl-11-[[3,4,6-trideoxy-3-(diMethylaMino)-β-D-xylo-hexopyranosyl]oxy]-1-oxa-6-azacyclopentadecan-15-one;CP 472295;Draxxin;Tulathromycin A, >=95%;Tulathrmycin A
CAS: 217500-96-4
MF: C41H79N3O12
MW: 806.084
EINECS:
Product Categories: Carbohydrates & Derivatives;Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals;API
Mol File: 217500-96-4.mol
Tulathromycin A Structure
Tulathromycin A Chemical Properties
density 1.17
Safety Information
MSDS Information
Tulathromycin A Usage And Synthesis
Chemical Properties White Solid

Details:

Tulathromycin A Usage And Synthesis
Chemical Properties White Solid
Uses Tulathromycin is a semi-synthetic erythromycin belonging to the ring expanded aza–erythromycins. Ring expansion improvedsthe acid lability of the parent erythromycins. Tulathromycin is regarded as the first of the triamilides, having a third amino (propylaminomethylene) group on a sugar to improve absorption. This modification provides a mixture of the two tulathromycin isomers (90:10) present in the commercial animal health product.
Uses Tulathromycin is a semi-synthetic erythromycin belonging to the ring expanded aza–erythromycins. Ring expansion improves the acid lability compared with the parent erythromycins. Tulathromycin is regarded as the first of the triamilides, having a third amino (propylaminomethylene) group on a sugar to improve absorption. This modification provides a mixture of the two tulathromycin isomers (90:10) present in the commercial animal health product.
Uses Triamilide antibiotic for treatment of bovine and porcine respiratory disease. Exists as an equilibrium mixture of two isomeric forms, Tulathromycin A (90%) and B (10%). Antibacterial.