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Vanillic acid
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Looking for Vanillic acid API 121-34-6?
- Description:
- Here you will find a list of producers, manufacturers and distributors of Vanillic acid. You can filter on certificates such as GMP, FDA, CEP, Written Confirmation and more. Send inquiries for free and get in direct contact with the supplier of your choice.
- API | Excipient name:
- Vanillic acid
- Synonyms:
- 4-Hydroxy-3-methoxybenzoic acid , VA
- Cas Number:
- 121-34-6
- DrugBank number:
- DB02130
- Unique Ingredient Identifier:
- GM8Q3JM2Y8
General Description:
Vanillic acid, identified by CAS number 121-34-6, is a notable compound with significant therapeutic applications. A flavoring agent. It is the intermediate product in the two-step bioconversion of ferulic acid to vanillin. (J Biotechnol 1996;50(2-3):107-13).
Classification:
Vanillic acid belongs to the class of organic compounds known as m-methoxybenzoic acids and derivatives. These are benzoic acids in which the hydrogen atom at position 3 of the benzene ring is replaced by a methoxy group, classified under the direct parent group M-methoxybenzoic acids and derivatives. This compound is a part of the Organic compounds, falling under the Benzenoids superclass, and categorized within the Benzene and substituted derivatives class, specifically within the Benzoic acids and derivatives subclass.
Categories:
Vanillic acid is categorized under the following therapeutic classes: Acids, Carbocyclic, Benzene Derivatives, Benzoates, Hydroxy Acids, Hydroxybenzoate Ethers, Hydroxybenzoates, Phenols, Phenyl Ethers. These classifications highlight the drug's diverse therapeutic applications and its importance in treating various conditions.
Experimental Properties:
Further physical and chemical characteristics of Vanillic acid include:
- Water Solubility: 1500 mg/L (at 14 °C)
- Melting Point: 211.5 °C
- logP: 1.43
- logS: -2.05
- pKa: 4.51 (at 25 °C)
Vanillic acid is a type of Intermediates
Pharmaceutical intermediates are a crucial category within the API (Active Pharmaceutical Ingredient) industry. These chemical compounds play a vital role in the synthesis of APIs, serving as building blocks or precursor molecules in the manufacturing process. Pharmaceutical intermediates are designed to undergo specific chemical transformations, enabling the production of targeted APIs with desired properties.
These intermediates are typically produced through complex organic synthesis, involving various chemical reactions and purification steps. They are carefully developed and optimized to ensure high purity, stability, and safety, meeting stringent regulatory requirements for pharmaceutical use.
Pharmaceutical intermediates offer several advantages in API production. Firstly, they enable the efficient and cost-effective synthesis of APIs by providing a well-defined starting material. This reduces the need for expensive or hard-to-obtain raw materials, streamlining the overall manufacturing process. Secondly, intermediates allow for fine-tuning of the chemical reactions, optimizing the yield and quality of the final API. This control over the synthesis process enhances the consistency and reproducibility of pharmaceutical manufacturing.
Moreover, pharmaceutical intermediates facilitate the development of new APIs and drug formulations. By modifying the structure or functional groups of the intermediate molecules, researchers can explore different chemical pathways and create novel compounds with improved therapeutic efficacy, reduced side effects, or enhanced bioavailability.
In summary, pharmaceutical intermediates are essential components in API synthesis, enabling efficient and controlled production of pharmaceutical compounds. Their versatility and role in driving innovation make them indispensable in the pharmaceutical industry.
