Synopsis
Synopsis
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API Suppliers
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USDMF
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CEP/COS
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JDMF
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EU WC
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KDMF
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NDC API
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VMF
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Listed Suppliers
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EDQM
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USP
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JP
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Others
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FDF Dossiers
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FDA Orange Book
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Europe
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Canada
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Australia
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South Africa
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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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US Patents
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US Exclusivities
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US Medicaid
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FDF
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Data Compilation #PharmaFlow
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1. 61508-36-9
2. Schembl1185698
3. Dtxsid70553331
4. Ujgxiastrimvrt-uhfffaoysa-n
5. Gs1168
6. Akos002671090
7. Da-20093
8. Methyl 5-(aminosulfonyl)-2-chlorobenzoate
9. En300-270496
10. F2126-0046
| Molecular Weight | 249.67 g/mol |
|---|---|
| Molecular Formula | C8H8ClNO4S |
| XLogP3 | 1.2 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 3 |
| Exact Mass | Da |
| Monoisotopic Mass | Da |
| Topological Polar Surface Area | 94.8 |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 337 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of GS1168 API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right GS1168 manufacturer or GS1168 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred GS1168 manufacturer or GS1168 supplier.
A GS1168 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of GS1168, including repackagers and relabelers. The FDA regulates GS1168 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. GS1168 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 GS1168 supplier is an individual or a company that provides GS1168 active pharmaceutical ingredient (API) or GS1168 finished formulations upon request. The GS1168 suppliers may include GS1168 API manufacturers, exporters, distributors and traders.
GS1168 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 GS1168 GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right GS1168 GMP manufacturer or GS1168 GMP API supplier for your needs.
A GS1168 CoA (Certificate of Analysis) is a formal document that attests to GS1168's compliance with GS1168 specifications and serves as a tool for batch-level quality control.
GS1168 CoA mostly includes findings from lab analyses of a specific batch. For each GS1168 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.
GS1168 may be tested according to a variety of international standards, such as European Pharmacopoeia (GS1168 EP), GS1168 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (GS1168 USP).
