Analytical Services
Analytical Services
ISP Standards ---
Purification Services
Science is the foundation of our Organisation
ISP can provide you a complete purification and analytical support for the production of pharmaceutical and functional products with our purification technology which we have developed over many years.We accept Custom/Contract purification services by using our facilities, such as preparative devices and columns developed for purification of Intermediates, APIs, Final products, racemic mixtures, from mg to kg level.
With our synthesised bulk packing materials (media), we provide total support services from separation method development to preparative isolation.
We can optimize methods, depending on the objective and required purity, and perform preparative purification using preparative LC systems and packing materials, developed and produced in-house.
In addition to ensuring qualification of target substances according to your request, we will also propose an efficient separation method that may result in a cost reduction, based on our past achievements and know-how.
Please feel free to contact our Lab about the feasibility study or selection of packing materials, column systems, etc. for isolation of your product.
Problems in Purification
- No Devices or Facilities
- Time, Cost, and Labour
- Difficulty in Purification Methods
- High Cost of Chromatography Media
Features ---
Analytical Services
. Highly-productive service with high efficiency preparative separation methods
. Vast experience on Separation and Purification
. Strong Knowledge on Column chemistries and selection
. Low cost purification services
. Highly-competitive service with low-cost column packing materials
. Availability of large columns and separation devices.
. Service corresponding to wide range of preparation scale (from small scale to large scale
Flow of purification service
We respond flexibly to your need including confidentiality, GMP requirements, and budget. Please feel free to ask for consultation about purification of any scale from small production to mass production.
1
Purification Request
- Consultation
- Signing a non-disclosure agreement
- Preliminary test, using customer-provided sample
2
Report for Preliminary Test Results
- Suggestions of optimal column and purification methods
3
Submission of Quotation
- After Preliminary Test a quotation will be shared
4
Actual purification
- Purification with optimal methods
5
Delivery of the purified material and reports
- Final Delivery of the material abd reports
Target Substances
Oligonucleotides
Peptides
Chiral Compounds
Active Pharmaceutical Ingredients (API)
Impurities
