Synopsis
Synopsis
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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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FDF Dossiers
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Listed Dossiers
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Regulatory FDF Prices
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FDF
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1. 6974-99-8
2. Nsc22053
3. 1h-indene,2,3-dihydro-2,4,7-trimethyl-
4. Dtxsid40281578
5. Zinc1589737
6. Nsc-22053
7. 1h-indene,3-dihydro-2,4,7-trimethyl-
8. Ds-002906
| Molecular Weight | 160.25 g/mol |
|---|---|
| Molecular Formula | C12H16 |
| XLogP3 | 3.7 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 0 |
| Exact Mass | 160.125200510 g/mol |
| Monoisotopic Mass | 160.125200510 g/mol |
| Topological Polar Surface Area | 0 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 143 |
| 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 |
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ABOUT THIS PAGE
44
PharmaCompass offers a list of Microcrystalline Cellulose API 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 Microcrystalline Cellulose API manufacturer or Microcrystalline Cellulose API supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Microcrystalline Cellulose API manufacturer or Microcrystalline Cellulose API supplier.
PharmaCompass also assists you with knowing the Microcrystalline Cellulose API API Price utilized in the formulation of products. Microcrystalline Cellulose API API Price is not always fixed or binding as the Microcrystalline Cellulose API Price is obtained through a variety of data sources. The Microcrystalline Cellulose API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Microcrystalline Cellulose manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Microcrystalline Cellulose, including repackagers and relabelers. The FDA regulates Microcrystalline Cellulose manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Microcrystalline Cellulose API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Microcrystalline Cellulose manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Microcrystalline Cellulose supplier is an individual or a company that provides Microcrystalline Cellulose active pharmaceutical ingredient (API) or Microcrystalline Cellulose finished formulations upon request. The Microcrystalline Cellulose suppliers may include Microcrystalline Cellulose API manufacturers, exporters, distributors and traders.
click here to find a list of Microcrystalline Cellulose suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Microcrystalline Cellulose DMF (Drug Master File) is a document detailing the whole manufacturing process of Microcrystalline Cellulose active pharmaceutical ingredient (API) in detail. Different forms of Microcrystalline Cellulose DMFs exist exist since differing nations have different regulations, such as Microcrystalline Cellulose USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Microcrystalline Cellulose DMF submitted to regulatory agencies in the US is known as a USDMF. Microcrystalline Cellulose USDMF includes data on Microcrystalline Cellulose's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Microcrystalline Cellulose USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Microcrystalline Cellulose suppliers with USDMF on PharmaCompass.
Microcrystalline Cellulose 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 Microcrystalline Cellulose 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 Microcrystalline Cellulose GMP manufacturer or Microcrystalline Cellulose GMP API supplier for your needs.
A Microcrystalline Cellulose CoA (Certificate of Analysis) is a formal document that attests to Microcrystalline Cellulose's compliance with Microcrystalline Cellulose specifications and serves as a tool for batch-level quality control.
Microcrystalline Cellulose CoA mostly includes findings from lab analyses of a specific batch. For each Microcrystalline Cellulose 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.
Microcrystalline Cellulose may be tested according to a variety of international standards, such as European Pharmacopoeia (Microcrystalline Cellulose EP), Microcrystalline Cellulose JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Microcrystalline Cellulose USP).
