Timolol EP Impurity E and Timolol BP Impurity E and Timolol USP RC E Manufacturer in Mumbai
- Timolol EP Impurity E \ Timolol BP Impurity E \ Timolol USP RC E
- CAT No : ALL-TIM-5
- Chemical Name : (2Z)-4-[(1S)-1-[[(1,1-Dimethylethyl)amino]methyl]-2-[[4-(morpholin-4-yl)-1,2,5-thiadiazol-3-yl]oxy]ethoxy]-4-oxobut-2-enoic acid maleate
- Molecular Formula : C17H26N4O6S ;C21H30N4O10S (maleate salt)
- Molecular Weight : 414.48 ;530.55
- CAS Number : 1026075-53-5 (base)
- Solubility : Methanol, DMSO
- Storage : 2-8 °C
- Keywords : Timolol EP Impurity E \ Timolol BP Impurity E \ Timolol USP RC E, (2Z)-4-[(1S)-1-[[(1,1-Dimethylethyl)amino]methyl]-2-[[4-(morpholin-4-yl)-1,2,5-thiadiazol-3-yl]oxy]ethoxy]-4-oxobut-2-enoic acid maleate
- Purity by HPLC : 95% +
COADocuments - COA, HNMR, 13CNMR, MASS, HPLC (by pharmacopoeia method with RT RRT results), IR and TGA will be provided with the purchase of Timolol EP Impurity E \ Timolol BP Impurity E \ Timolol USP RC E
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Allmpus laboratories private limited (Based in India) are in Business for science & innovation, it is continuously involved in design, research , development with cost effective synthesis and finding out new techniques of isolation & purification.
For Business Queries
ashish@allmpus.comFor Career Related Queries
girish@allmpus.comOur Locations
Corporate Office
Mumbai Maharashtra, India
R&D Centers
Amravati, Maharashtra, India
Manufacturing Plant
Amravati, Maharashtra, India
Services
- Contract Research
- Synthesis of API related Compound, Process Impurity, Metabolite and are acceptable to all regulatory agencies & also used for ANDA filing /DMF filing and genotoxic study.
- Synthesis of NCE’S
- Synthesis of Medicinal library
- Synthesis of Molecules for SAR studies
- Synthesis of references compound and scale up to kg scale.
- Analytical Support