Synopsis
Synopsis
0
API Suppliers
0
USDMF
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Listed Suppliers
0
EDQM
0
USP
0
JP
0
Others
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
US Medicaid
NA
Annual Reports
NA
Regulatory FDF Prices
NA
0
API
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
1. Schembl2421535
2. (+)-3-(2,3-difluorophenyl)-3-methoxypyrrolidine
3. (-)-3-(2,3-difluorophenyl)-3-methoxypyrrolidine
| Molecular Weight | 213.22 g/mol |
|---|---|
| Molecular Formula | C11H13F2NO |
| XLogP3 | 1.3 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 2 |
| Exact Mass | 213.09652036 g/mol |
| Monoisotopic Mass | 213.09652036 g/mol |
| Topological Polar Surface Area | 21.3 Ų |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 227 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
21
PharmaCompass offers a list of IRL752 API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right IRL752 manufacturer or IRL752 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred IRL752 manufacturer or IRL752 supplier.
PharmaCompass also assists you with knowing the IRL752 API Price utilized in the formulation of products. IRL752 API Price is not always fixed or binding as the IRL752 Price is obtained through a variety of data sources. The IRL752 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A IRL752 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of IRL752, including repackagers and relabelers. The FDA regulates IRL752 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. IRL752 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A IRL752 supplier is an individual or a company that provides IRL752 active pharmaceutical ingredient (API) or IRL752 finished formulations upon request. The IRL752 suppliers may include IRL752 API manufacturers, exporters, distributors and traders.
IRL752 Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of IRL752 GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right IRL752 GMP manufacturer or IRL752 GMP API supplier for your needs.
A IRL752 CoA (Certificate of Analysis) is a formal document that attests to IRL752's compliance with IRL752 specifications and serves as a tool for batch-level quality control.
IRL752 CoA mostly includes findings from lab analyses of a specific batch. For each IRL752 CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
IRL752 may be tested according to a variety of international standards, such as European Pharmacopoeia (IRL752 EP), IRL752 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (IRL752 USP).
