Synopsis
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1. Dicyclopentadienyliron
2. Ferrocene
1. U96pkg90jq
2. Ccris 3195
3. Hsdb 2878
4. Einecs 203-039-3
5. Unii-u96pkg90jq
6. Ai3-23119
7. Ferrocene [mi]
8. Ferrocene [hsdb]
9. Dsstox_cid_5326
10. Ec 203-039-3
11. Dsstox_rid_77749
12. Dsstox_gsid_25326
13. Bis( Cyclopentadienyl)eisen(ii)
14. Tox21_202514
15. Ncgc00091936-01
16. Ncgc00260063-01
17. Cas-102-54-5
18. Q211972
19. Bis(cyclopentadienyl)iron, Di(cyclopentadienyl)iron
| Molecular Weight | 186.03 g/mol |
|---|---|
| Molecular Formula | C10H10Fe |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 186.013186 g/mol |
| Monoisotopic Mass | 186.013186 g/mol |
| Topological Polar Surface Area | 0 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 11.6 |
| 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 |
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USDMF
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ABOUT THIS PAGE
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PharmaCompass offers a list of Ferrocene 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 Ferrocene manufacturer or Ferrocene supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ferrocene manufacturer or Ferrocene supplier.
PharmaCompass also assists you with knowing the Ferrocene API Price utilized in the formulation of products. Ferrocene API Price is not always fixed or binding as the Ferrocene Price is obtained through a variety of data sources. The Ferrocene Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tox21_202514 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_202514, including repackagers and relabelers. The FDA regulates Tox21_202514 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_202514 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 Tox21_202514 supplier is an individual or a company that provides Tox21_202514 active pharmaceutical ingredient (API) or Tox21_202514 finished formulations upon request. The Tox21_202514 suppliers may include Tox21_202514 API manufacturers, exporters, distributors and traders.
click here to find a list of Tox21_202514 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tox21_202514 DMF (Drug Master File) is a document detailing the whole manufacturing process of Tox21_202514 active pharmaceutical ingredient (API) in detail. Different forms of Tox21_202514 DMFs exist exist since differing nations have different regulations, such as Tox21_202514 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tox21_202514 DMF submitted to regulatory agencies in the US is known as a USDMF. Tox21_202514 USDMF includes data on Tox21_202514's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tox21_202514 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Tox21_202514 suppliers with USDMF on PharmaCompass.
Tox21_202514 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 Tox21_202514 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 Tox21_202514 GMP manufacturer or Tox21_202514 GMP API supplier for your needs.
A Tox21_202514 CoA (Certificate of Analysis) is a formal document that attests to Tox21_202514's compliance with Tox21_202514 specifications and serves as a tool for batch-level quality control.
Tox21_202514 CoA mostly includes findings from lab analyses of a specific batch. For each Tox21_202514 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.
Tox21_202514 may be tested according to a variety of international standards, such as European Pharmacopoeia (Tox21_202514 EP), Tox21_202514 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tox21_202514 USP).
