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1. Erythrityl Tetranitrate
2. Tetranitrate, Erythrityl
1. Erythrityl Tetranitrate
2. Cardiloid
3. Cardivell
4. Cardiwell
5. Erythritetranitrat
6. 1,3,4-trinitrooxybutan-2-yl Nitrate
7. Erythritol, Tetranitrate
8. 7297-25-8
9. Schembl613474
10. Chembl453636
11. 1,2,3,4-butanetetrayl Nitrate
12. Dtxsid20860007
13. 1,3,4-butanetetralyl Tetranitrate
14. Nsc106566
15. Butane-1,2,3,4-tetrayl Tetranitrate
16. 643-97-0
17. 1,3,4-butanetetrol, Tetranitrate, (r*,s*)-
| Molecular Weight | 302.11 g/mol |
|---|---|
| Molecular Formula | C4H6N4O12 |
| XLogP3 | 1.4 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 12 |
| Rotatable Bond Count | 7 |
| Exact Mass | 301.99822164 g/mol |
| Monoisotopic Mass | 301.99822164 g/mol |
| Topological Polar Surface Area | 220 Ų |
| Heavy Atom Count | 20 |
| Formal Charge | 0 |
| Complexity | 326 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 2 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
Vasodilator Agents
Drugs used to cause dilation of the blood vessels. (See all compounds classified as Vasodilator Agents.)
ABOUT THIS PAGE
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Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Erythrityl Tetranitrate manufacturer or Erythrityl Tetranitrate supplier.
A Cardiloid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cardiloid, including repackagers and relabelers. The FDA regulates Cardiloid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cardiloid 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 Cardiloid supplier is an individual or a company that provides Cardiloid active pharmaceutical ingredient (API) or Cardiloid finished formulations upon request. The Cardiloid suppliers may include Cardiloid API manufacturers, exporters, distributors and traders.
click here to find a list of Cardiloid suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Cardiloid DMF (Drug Master File) is a document detailing the whole manufacturing process of Cardiloid active pharmaceutical ingredient (API) in detail. Different forms of Cardiloid DMFs exist exist since differing nations have different regulations, such as Cardiloid USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cardiloid DMF submitted to regulatory agencies in the US is known as a USDMF. Cardiloid USDMF includes data on Cardiloid's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cardiloid USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cardiloid suppliers with USDMF on PharmaCompass.
Cardiloid 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 Cardiloid GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Cardiloid GMP manufacturer or Cardiloid GMP API supplier for your needs.
A Cardiloid CoA (Certificate of Analysis) is a formal document that attests to Cardiloid's compliance with Cardiloid specifications and serves as a tool for batch-level quality control.
Cardiloid CoA mostly includes findings from lab analyses of a specific batch. For each Cardiloid 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.
Cardiloid may be tested according to a variety of international standards, such as European Pharmacopoeia (Cardiloid EP), Cardiloid JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cardiloid USP).