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Specifications
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Appearance |
White to yellow solid |
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Purity (GC) |
98% min |
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Water |
1% max |
Transport Information
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Parameter |
Specification |
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UN Number |
3261 |
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Class |
8 |
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Packing Group |
II |
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H.S. Code |
2915900090307 |
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Stability & Reactivity |
The product is chemically stable under standard ambient conditions. |
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Storage |
Tightly closed. Store in a closed, dry, ventilated place. Keep away from open flames, hot surfaces and sources of ignition. |
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Condition to Avoid |
Strong oxidizing agents |
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Package |
Manufacturing Information
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Parameter |
Specification |
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Capacity |
10MT/month |
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Frequency |
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Main Export Countries |
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Capacity/Batch |
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Experience |
Production since 2013 |
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Stock |
Applications of 3-Bromopropionic acid丨CAS 590-92-1
1. Pharmaceutical Research and Development
● Key intermediate in the synthesis of various bioactive molecules.
● Studied for its potential as an anticancer agent, particularly for its inhibition of glycolysis in cancer cells by targeting the enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH).
● Utilized in the synthesis of small-molecule inhibitors and prodrugs.
2. Biochemical and Cancer Research
● Used as a tool compound to explore cancer cell metabolism and mitochondrial function.
● 3-Bromopropionic acid (3-BP) selectively inhibits ATP production in cancer cells, leading to metabolic collapse-an area of active investigation for metabolic targeting in oncology.
● Has shown potential in preclinical studies as a tumor-selective anticancer agent.
3. Organic Synthesis Intermediate
● 3-Bromopropionic acid丨CAS 590-92-1 serves as a building block for the preparation of:
o Amino acids
o Esters
o Peptides
o Heterocyclic compounds
● Used to introduce the bromoalkyl functional group in custom synthesis strategies.
4. Polymer and Material Science
● Can be chemically modified to serve as a monomer or crosslinker in specialty polymers.
● Functional groups (carboxylic acid and alkyl bromide) enable incorporation into reactive polymer backbones.
Benefits
1. Bifunctional Reactivity
● Contains both a reactive bromine atom and a carboxylic acid group, offering dual reactivity:
o The bromine allows for nucleophilic substitution, alkylation, or halogen exchange.
o The acid group allows for esterification, amide formation, or metal coordination.
● Ideal for stepwise functionalization in synthetic chemistry.
2. Biological Selectivity
● In studies, 3-BP shows selectivity for cancer cells due to their altered metabolism (Warburg effect).
● This makes it a promising lead compound for targeted therapeutic development with minimal effects on normal cells.
3. Versatility as a Chemical Intermediate
● Compatible with a wide range of synthetic transformations, making it valuable in both medicinal chemistry and material science.
● Its structural simplicity supports derivatization into complex molecules.
Conclusion
3-Bromopropionic acid丨CAS 590-92-1 is a versatile organobromine compound with broad applications in organic synthesis, pharmaceutical R&D, and biochemical research. Its dual-functional nature and bioactivity make it a valuable tool in cancer metabolism studies and a promising scaffold for drug development. Despite requiring careful handling due to its reactive and potentially toxic nature, its utility in both laboratory and industrial contexts continues to grow.

