Mutilin
- Product Name
- Mutilin
- CAS No.
- 6040-37-5
- Chemical Name
- Mutilin
- Synonyms
- Mutilin;Tiamulin EP Impurity A;Mutilin (Tiamulin EP Impurity A);(3aS,4R,5S,6S,8R,9R,9aR,10R)-6-Ethe;Tiamulin Hydrogen Fumarate Impurity A;Tiamulin Hydrogen Fumarate EP Impurity A;3a,9-Propano-3aH-cyclopentacycloocten-1(4H)-one, 6-ethenyloctahydro-5,8-dihydroxy-4,6,9,10-tetramethyl-, (3aS,4R,5S,6S,8R,9R,9aR,10R)-;(3aR,4R,5R,7S,8S,9R,9aS,12R)-5,8-Dihydroxy-4,7,9,12-tetramethyl-7-vinyloctahydro-4,9a-propanocyclopenta[8]annulen-3(3aH)-one (Mutilin (Tiamulin) Impurity)
- CBNumber
- CB12703748
- Molecular Formula
- C20H32O3
- Formula Weight
- 320.47
- MOL File
- 6040-37-5.mol
Mutilin Property
- Melting point:
- 68-70 °C
- Boiling point:
- 427.7±45.0 °C(Predicted)
- Density
- 1.09±0.1 g/cm3(Predicted)
- storage temp.
- Hygroscopic, -20°C Freezer, Under inert atmosphere
- solubility
- Chloroform (Sparingly, Sonicated), Ethyl Acetate (Slightly)
- pka
- 14.61±0.70(Predicted)
- form
- Solid
- color
- Off-White
- Stability:
- Hygroscopic
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H319Causes serious eye irritation
- Precautionary statements
-
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P337+P313IF eye irritation persists: Get medical advice/attention.
N-Bromosuccinimide Price
- Product number
- 456707
- Product name
- Mutilin
- Packaging
- 25mg
- Price
- $460
- Updated
- 2021/12/16
- Product number
- M820050
- Product name
- Mutilin
- Packaging
- 250mg
- Price
- $1455
- Updated
- 2021/12/16
- Product number
- 66347
- Product name
- Mutilin
- Packaging
- 25mg
- Price
- $650
- Updated
- 2021/12/16
Mutilin Chemical Properties,Usage,Production
Uses
Mutilin is minor metabolite of the pleuromutilin family, originally isolated from Pleurotus mutilus. Mutilin is formed by hydrolysis of the hydroxyacetyl ester of pleuromutilin, and is a degradation product and in vivo metabolite of pleuromutilin. Interest in mutilin has focused on its potential as a substrate for generating unique metabolites via biosynthesis to provide a broader range of targets for semi-synthetic modification.
Uses
Mutilin, is used to perform biological studies with focus on antimicrobial activity. This complex is also a reagent in the production of pleuromutilin derivatives.