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
API
0
FDF
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
EDQM
0
USP
0
JP
0
Others
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
1. 6001-64-5
2. 1,1,1-trichloro-2-methyl-2-propanol Hemihydrate
3. 1,1,1-trichloro-2-methylpropan-2-ol;hydrate
4. Chlorbutanol Hemihydrate
5. 2-propanol, 1,1,1-trichloro-2-methyl-, Hydrate (2:1)
6. 3x4p6271ox
7. Nsc-760101
8. Unii-3x4p6271ox
9. 1,1,1-trichloro-2-methyl-2-propanol(hydrate) (2:1)
10. Acetonchloroform Hemihydrate
11. Bis(1,1,1-trichloro-2-methylpropan-2-ol) Hydrate
12. Schembl466638
13. 2-propanol, 1,1,1-trichloro-2-methyl-, Hemihydrate
14. 1,1,1-trichloro-2-methyl-2-propanol (hydrate) (2:1)
15. 1,1,1-trichloro-2-methyl-2-propanolhemihydrate
16. Dtxsid9022235
17. Beta,beta,beta-trichloro-t-butanol
18. Mfcd02179352
19. Chlorobutanol Hemihydrate [ii]
20. Akos016015222
21. Nsc 760101
22. Chlorobutanol Hemihydrate [who-dd]
23. Chlorobutanol Hemihydrate [who-ip]
24. Chlorobutanol Hemihydrate [ep Monograph]
25. A917946
26. Q27258164
27. 1,1,1-trichloro-2-methyl-2-propanol Hemihydrate, 98%
28. Chlorobutanol, United States Pharmacopeia (usp) Reference Standard
29. 1,1,1-trichloro-2-methyl-2-propanol Hemihydrate, Pestanal(r), Analytical Standard
30. Chlorobutanol, Pharmaceutical Secondary Standard; Certified Reference Material
31. 1,1,1-trichloro-2-methyl-2-propanol Hemihydrate, Meets Analytical Specification Of Ph.??eur., Bp, Nf, 98-100.5% (calc With Ref. To Anhyd. Subst.)
| Molecular Weight | 372.9 g/mol |
|---|---|
| Molecular Formula | C8H16Cl6O3 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 371.920110 g/mol |
| Monoisotopic Mass | 369.923061 g/mol |
| Topological Polar Surface Area | 41.5 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 83.8 |
| 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 | 3 |
ABOUT THIS PAGE
A Acetonchloroform Hemihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acetonchloroform Hemihydrate, including repackagers and relabelers. The FDA regulates Acetonchloroform Hemihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acetonchloroform Hemihydrate 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 Acetonchloroform Hemihydrate supplier is an individual or a company that provides Acetonchloroform Hemihydrate active pharmaceutical ingredient (API) or Acetonchloroform Hemihydrate finished formulations upon request. The Acetonchloroform Hemihydrate suppliers may include Acetonchloroform Hemihydrate API manufacturers, exporters, distributors and traders.
Acetonchloroform Hemihydrate 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 Acetonchloroform Hemihydrate 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 Acetonchloroform Hemihydrate GMP manufacturer or Acetonchloroform Hemihydrate GMP API supplier for your needs.
A Acetonchloroform Hemihydrate CoA (Certificate of Analysis) is a formal document that attests to Acetonchloroform Hemihydrate's compliance with Acetonchloroform Hemihydrate specifications and serves as a tool for batch-level quality control.
Acetonchloroform Hemihydrate CoA mostly includes findings from lab analyses of a specific batch. For each Acetonchloroform Hemihydrate 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.
Acetonchloroform Hemihydrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Acetonchloroform Hemihydrate EP), Acetonchloroform Hemihydrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Acetonchloroform Hemihydrate USP).
LOOKING FOR A SUPPLIER?
