AgrochemicalsBromoxynil Impurity 3
Original price was: ₹60,000.00.₹50,000.00Current price is: ₹50,000.00.
Bromoxynil Impurity 3
Name:3,5-Dibromo-4-hydroxybenzoic Acid
CAT. NO.:SAB-09-C
CAS NO.:3337-62-0
- Description
- Datasheet
- Additional information
Description
Bromoxynil Impurity 3
Chemical Name | 3,5-Dibromo-4-hydroxybenzoic Acid |
Catalog Number | SAB-09-C |
Parent AI | Bromoxynil |
Synonyms | Bromoxynil Acid; Bromoxynilbenzoic Acid; NSC 21184 |
CAS Number | 3337-62-0 |
Molecular Formula | C₇H₄Br₂O₃ |
Molecular Weight | 295.91 |
Appearance | White to Off-White Solid |
Melting Point | >246ºC (subl.) |
Shipping & Storage Information
|
Storage 4°C, Inert atmosphere
Shipping: Free Shipping at Room Temperature in INDIA, may vary elsewhere Stability: Datasheet |
Solubility | DMSO (Sparingly), Methanol (Slightly) |
Stability | Stable under recommended storage conditions |
Category | Building Blocks; Miscellaneous |
Description &Applications | 3,5-Dibromo-4-hydroxybenzoic acid (DBHBA) is an organic compound with the chemical formula C7H4Br2O3. It is a white, crystalline solid that is soluble in water and other polar organic solvents. DBHBA is a versatile chemical compound with a wide range of applications in the fields of chemistry and biochemistry. It is used as a reagent in organic synthesis, as a biological stain, and as an inhibitor of certain enzymes. In addition, DBHBA has been studied for its potential use in drug delivery systems and as a therapeutic agent. |
References | He, G., et al.: Faming Zhuanli Shenqing, CN 103242272 A 20130814 (2013); Heel, R.C. et al.: Drugs, 14, 349 (1977); Perez-Ruiz, F. et al.: Ann. Rheum. Dis., 57, 545 (1998) |
3,5-Dibromo-4-hydroxybenzoic Acid, a compound that holds remarkable properties and potential applications across various scientific realms. In this exploration, we delve into the structure, synthesis, properties, and potential applications of this intriguing compound.
Structure and Synthesis: 3,5-Dibromo-4-hydroxybenzoic Acid, often abbreviated as DBHBA, belongs to the family of benzoic acids, which are aromatic compounds bearing a carboxylic acid functional group. Its chemical formula is C7H4Br2O3, and its structure consists of a benzene ring substituted with two bromine atoms and a hydroxyl (OH) group, along with a carboxylic acid (COOH) group. The arrangement of these atoms gives DBHBA its distinct properties and reactivity.
The synthesis of 3,5-Dibromo-4-hydroxybenzoic Acid typically involves chemical reactions that introduce the bromine atoms and the hydroxyl group onto the benzene ring. Various methods, such as bromination and hydroxylation, can be employed to achieve this synthesis, often requiring precise control of reaction conditions and reagents.
Properties and Applications: The unique combination of bromine atoms and hydroxyl group on the benzene ring grants 3,5-Dibromo-4-hydroxybenzoic Acid its distinctive physical and chemical properties. It is a crystalline solid with a pale yellow color, and its solubility varies depending on the solvent and conditions. The compound can exhibit intriguing behaviors, such as forming hydrogen bonds and undergoing various types of reactions.
The diverse properties of DBHBA open up a range of potential applications in different fields:
1. Medicinal Chemistry: DBHBA’s structural features make it an interesting candidate for drug development and pharmaceutical research. Its ability to interact with biological molecules through hydrogen bonding and other interactions could lead to the design of new therapeutic agents. Researchers might explore its potential as an anti-inflammatory or anti-cancer agent, leveraging its unique structure for targeted interactions with specific cellular components.
2. Materials Science: With its distinctive properties, 3,5-Dibromo-4-hydroxybenzoic Acid could find use in materials science. It might be incorporated into polymer matrices to enhance their mechanical properties or act as a functional group for surface modification. Its ability to form hydrogen bonds might facilitate the creation of novel materials with improved adhesion or other tailored characteristics.
3. Organic Synthesis: The reactivity of DBHBA could be harnessed in organic synthesis as a building block or a catalyst. Its unique substitution pattern could influence the outcome of reactions, leading to the creation of complex molecules with specific stereochemistry or functionality.
4. Analytical Chemistry: The compound’s distinct spectral properties, such as UV-visible absorption and infrared spectroscopy, could make it valuable in analytical techniques. It might serve as a standard or reference compound for calibration purposes or as a probe to study specific chemical environments.
Additional information
Pack Size | 50mg |
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