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. Dibutyl Sulphite
2. 626-85-7
3. Sulfurous Acid, Dibutyl Ester
4. Butyl Sulfite (bu2so3)
5. Butyl Sulfite
6. Sulfurous Acid Dibutyl Ester
7. U7nw3u1v9m
8. Nsc-2587
9. Dibutylsulfit
10. Nsc 2587
11. Einecs 210-965-1
12. Di-n-butyl Sulphite
13. Unii-u7nw3u1v9m
14. Sulphurous Acid Dibutyl Ester
15. Schembl775328
16. Dtxsid3060825
17. Butyl Sulfite, (buo)2so
18. Nsc2587
19. Zinc1641014
20. Ft-0656171
21. A833926
| Molecular Weight | 194.29 g/mol |
|---|---|
| Molecular Formula | C8H18O3S |
| XLogP3 | 2.7 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 8 |
| Exact Mass | 194.09766561 g/mol |
| Monoisotopic Mass | 194.09766561 g/mol |
| Topological Polar Surface Area | 54.7 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 105 |
| 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
50
PharmaCompass offers a list of Dibutyl Sulfite 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 Dibutyl Sulfite manufacturer or Dibutyl Sulfite supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dibutyl Sulfite manufacturer or Dibutyl Sulfite supplier.
PharmaCompass also assists you with knowing the Dibutyl Sulfite API Price utilized in the formulation of products. Dibutyl Sulfite API Price is not always fixed or binding as the Dibutyl Sulfite Price is obtained through a variety of data sources. The Dibutyl Sulfite Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dibutyl Sulfite manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dibutyl Sulfite, including repackagers and relabelers. The FDA regulates Dibutyl Sulfite manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dibutyl Sulfite 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 Dibutyl Sulfite supplier is an individual or a company that provides Dibutyl Sulfite active pharmaceutical ingredient (API) or Dibutyl Sulfite finished formulations upon request. The Dibutyl Sulfite suppliers may include Dibutyl Sulfite API manufacturers, exporters, distributors and traders.
Dibutyl Sulfite 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 Dibutyl Sulfite 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 Dibutyl Sulfite GMP manufacturer or Dibutyl Sulfite GMP API supplier for your needs.
A Dibutyl Sulfite CoA (Certificate of Analysis) is a formal document that attests to Dibutyl Sulfite's compliance with Dibutyl Sulfite specifications and serves as a tool for batch-level quality control.
Dibutyl Sulfite CoA mostly includes findings from lab analyses of a specific batch. For each Dibutyl Sulfite 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.
Dibutyl Sulfite may be tested according to a variety of international standards, such as European Pharmacopoeia (Dibutyl Sulfite EP), Dibutyl Sulfite JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Dibutyl Sulfite USP).
