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1. Polybutylene
1. Polybutenes
2. 9003-29-6
3. But-1-ene;(e)-but-2-ene
4. 119275-53-5
5. 1-butene,polymerwith2-buteneand2-methyl-1-propene,ep.
6. 1-butene 2-butene
7. Indopol H-100
8. Hsdb 5127
9. (2e)-but-2-ene; But-1-ene
10. Einecs 246-689-3
11. 1-butene, Polymer With 2-butene And 2-methyl-1-propene, Epoxidized
12. Un1012
13. Akos015915750
14. Butylene [un1012] [flammable Gas]
15. Ec 246-689-3
16. Polybutenes, Average Mn ~320, Isobutylene >90 %
17. Polybutenes, Average Mn ~460 By Vpo, Isobutylene >90 %
18. Polybutenes, Average Mn ~560 By Vpo, Isobutylene >90 %
19. Polybutenes, Average Mn ~920 By Vpo, Isobutylene >90 %
20. Polybutenes, Average Mn ~1,290 By Vpo, >90% In Isobutylene
21. Polybutenes, Average Mn ~2,300 By Vpo, Isobutylene >90 %
| Molecular Weight | 112.21 g/mol |
|---|---|
| Molecular Formula | C8H16 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 1 |
| Exact Mass | 112.125200510 g/mol |
| Monoisotopic Mass | 112.125200510 g/mol |
| Topological Polar Surface Area | 0 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 29.2 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
Market Place
ABOUT THIS PAGE
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PharmaCompass offers a list of Polybutene 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 Polybutene manufacturer or Polybutene supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Polybutene manufacturer or Polybutene supplier.
PharmaCompass also assists you with knowing the Polybutene API Price utilized in the formulation of products. Polybutene API Price is not always fixed or binding as the Polybutene Price is obtained through a variety of data sources. The Polybutene Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Indopol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Indopol, including repackagers and relabelers. The FDA regulates Indopol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Indopol 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 Indopol supplier is an individual or a company that provides Indopol active pharmaceutical ingredient (API) or Indopol finished formulations upon request. The Indopol suppliers may include Indopol API manufacturers, exporters, distributors and traders.
Indopol 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 Indopol 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 Indopol GMP manufacturer or Indopol GMP API supplier for your needs.
A Indopol CoA (Certificate of Analysis) is a formal document that attests to Indopol's compliance with Indopol specifications and serves as a tool for batch-level quality control.
Indopol CoA mostly includes findings from lab analyses of a specific batch. For each Indopol 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.
Indopol may be tested according to a variety of international standards, such as European Pharmacopoeia (Indopol EP), Indopol JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Indopol USP).
