Synopsis
Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
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. Triacetylcellulose
1. Triacetylcellulose
2. 9012-09-3
3. Beta-cellotriose Undecaacetate
4. Chebi:53498
5. Zinc169639103
| Molecular Weight | 966.8 g/mol |
|---|---|
| Molecular Formula | C40H54O27 |
| XLogP3 | -1.1 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 27 |
| Rotatable Bond Count | 29 |
| Exact Mass | 966.28524644 g/mol |
| Monoisotopic Mass | 966.28524644 g/mol |
| Topological Polar Surface Area | 335 Ų |
| Heavy Atom Count | 67 |
| Formal Charge | 0 |
| Complexity | 1850 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 15 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
Indicators and Reagents
Substances used for the detection, identification, analysis, etc. of chemical, biological, or pathologic processes or conditions. Indicators are substances that change in physical appearance, e.g., color, at or approaching the endpoint of a chemical titration, e.g., on the passage between acidity and alkalinity. Reagents are substances used for the detection or determination of another substance by chemical or microscopical means, especially analysis. Types of reagents are precipitants, solvents, oxidizers, reducers, fluxes, and colorimetric reagents. (From Grant and Hackh's Chemical Dictionary, 5th ed, p301, p499) (See all compounds classified as Indicators and Reagents.)
API SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
Market Place
ABOUT THIS PAGE
A Cellulose Triacetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cellulose Triacetate, including repackagers and relabelers. The FDA regulates Cellulose Triacetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cellulose Triacetate 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 Cellulose Triacetate supplier is an individual or a company that provides Cellulose Triacetate active pharmaceutical ingredient (API) or Cellulose Triacetate finished formulations upon request. The Cellulose Triacetate suppliers may include Cellulose Triacetate API manufacturers, exporters, distributors and traders.
click here to find a list of Cellulose Triacetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cellulose Triacetate DMF (Drug Master File) is a document detailing the whole manufacturing process of Cellulose Triacetate active pharmaceutical ingredient (API) in detail. Different forms of Cellulose Triacetate DMFs exist exist since differing nations have different regulations, such as Cellulose Triacetate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cellulose Triacetate DMF submitted to regulatory agencies in the US is known as a USDMF. Cellulose Triacetate USDMF includes data on Cellulose Triacetate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cellulose Triacetate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cellulose Triacetate suppliers with USDMF on PharmaCompass.
Cellulose Triacetate 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 Cellulose Triacetate 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 Cellulose Triacetate GMP manufacturer or Cellulose Triacetate GMP API supplier for your needs.
A Cellulose Triacetate CoA (Certificate of Analysis) is a formal document that attests to Cellulose Triacetate's compliance with Cellulose Triacetate specifications and serves as a tool for batch-level quality control.
Cellulose Triacetate CoA mostly includes findings from lab analyses of a specific batch. For each Cellulose Triacetate 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.
Cellulose Triacetate may be tested according to a variety of international standards, such as European Pharmacopoeia (Cellulose Triacetate EP), Cellulose Triacetate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cellulose Triacetate USP).
LOOKING FOR A SUPPLIER?
