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Specifications of 4-(4-Hydroxymethyl-3-methoxyphenoxy)butyric acid丨CAS 136849-75-7
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Identification |
The HNMR spectrum conforms to standard |
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Description |
Light yellow liquid or light yellow solid |
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Purity (HPLC) |
98.0% min |
Transport Information of 4-(4-Hydroxymethyl-3-methoxyphenoxy)butyric acid丨CAS 136849-75-7
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H.S. Code |
2933599099304 |
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Stability & Reactivity |
The product is chemically stable under standard ambient conditions (room temperature). |
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Storage |
Tightly closed. Store in a closed, dry, ventilated place |
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Condition to Avoid |
Keep away moisture. Strong heating. |
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Package |
As per request |
Manufacturing Information of 4-(4-Hydroxymethyl-3-methoxyphenoxy)butyric acid丨CAS 136849-75-7
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Experience |
Production since 2020 |
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Overview
4-(4-Hydroxymethyl-3-methoxyphenoxy)butyric acid丨CAS 136849-75-7 is an aromatic compound that consists of a butyric acid core (a short-chain fatty acid) attached to a phenyl group substituted with both a hydroxymethyl group and a methoxy group. The structural features suggest it may possess bioactive properties due to the functional groups (hydroxymethyl and methoxy) on the aromatic ring, which are known to influence biological interactions and solubility.
Applications of 4-(4-Hydroxymethyl-3-methoxyphenoxy)butyric acid丨CAS 136849-75-7
1. Drug Development and Pharmaceutical Research
● Potential Bioactive Compound: The presence of the methoxy and hydroxymethyl groups suggests that this compound may exhibit bioactivity, making it a candidate for pharmacological research. The butyric acid portion of the molecule might be involved in various metabolic pathways or cell signaling, potentially offering therapeutic benefits in areas like anti-inflammatory treatments, antioxidant therapy, or other metabolic conditions.
● Prodrug Development: The compound's structure suggests that it might be modified to create prodrugs for controlled release or targeted delivery of active compounds, especially considering the presence of a carboxyl group that can be modified for esterification.
2. Antioxidant and Anti-inflammatory Properties
● Potential Antioxidant: The methoxy group is a well-known electron-donating group, and phenolic compounds with such groups often show antioxidant activities. This suggests that 4-(4-Hydroxymethyl-3-methoxyphenoxy)butyric acid could be explored for antioxidant properties.
● Anti-inflammatory Research: The combination of the butyric acid group and the hydroxymethyl/methoxy substitution on the aromatic ring may indicate potential anti-inflammatory effects. It could be studied in the context of reducing inflammation or regulating immune response.
3. Research in Plant Metabolites and Natural Products
● Plant-Based Metabolite Analogue: The compound's structure suggests it could be related to naturally occurring phenolic metabolites found in plants. This could make it useful in research focused on plant-derived compounds with potential health benefits, such as in herbal medicine or the study of bioactive plant chemicals.
● Structure-Activity Relationship (SAR) Studies: It may be valuable in SAR studies to explore how modifications of the hydroxymethyl and methoxy groups affect the biological activity of phenolic compounds. This can help in designing compounds with improved efficacy for pharmacological or biotechnological applications.
4. Biochemical and Biophysical Research
● Molecular Interactions: Due to its aromatic structure, 4-(4-Hydroxymethyl-3-methoxyphenoxy)butyric acid丨CAS 136849-75-7 may interact with enzymes or receptors that bind to phenolic compounds or lipid-based molecules. Researchers may explore its binding affinity to specific targets, which could be valuable in drug screening and identifying new molecular targets.
● Peptide/Protein Binding: The structure of 4-(4-Hydroxymethyl-3-methoxyphenoxy)butyric acid could enable it to interact with peptides or proteins, making it relevant for studies in protein-ligand interactions or enzyme inhibition.
5. Cosmetic and Personal Care Applications
● Antioxidant in Skincare: Given the antioxidant potential indicated by its aromatic structure and methoxy group, the compound may find applications in cosmetic formulations designed to protect the skin from free radical damage or UV radiation. It could be included in anti-aging creams or skin care products to enhance the skin's resilience to oxidative stress.
● Anti-inflammatory Effects for Skin Health: The compound could also be explored for its potential anti-inflammatory properties in products aimed at treating skin irritation, redness, or conditions like eczema or psoriasis.
Benefits of 4-(4-Hydroxymethyl-3-methoxyphenoxy)butyric acid丨CAS 136849-75-7
√ Potential Bioactivity
● The molecule's methoxy and hydroxymethyl groups suggest it may exhibit antioxidant, anti-inflammatory, or other biological activities, making it useful in pharmaceutical and health-related applications.
√ Pharmaceutical and Drug Development Potential
● Its structure offers potential for drug development, either as a direct therapeutic agent or as part of a prodrug design, particularly for applications targeting metabolic disorders, inflammation, or oxidative stress.
√ Research in Molecular Interactions
● This compound can serve as an excellent candidate for SAR studies and protein-ligand interaction research, providing insights into how aromatic compounds interact with biological systems, which is valuable for the development of targeted therapies.
√ Cosmetic Applications
● The compound's antioxidant and potential anti-inflammatory properties may be beneficial in cosmetic formulations, promoting skin health and protection from oxidative damage or environmental stressors.
√ Plant-Derived Chemical Research
● Its structural similarity to natural plant-based phenolic compounds makes it an interesting subject for natural product research, possibly helping to unlock new plant-based therapies or bioactive compounds.
Conclusion
4-(4-Hydroxymethyl-3-methoxyphenoxy)butyric acid丨CAS 136849-75-7 is a bioactive compound with a promising range of pharmaceutical, biochemical, and cosmetic applications. Its unique structural features, including the hydroxymethyl and methoxy substitutions, suggest potential antioxidant and anti-inflammatory properties. It holds promise for use in drug development, particularly for targeting metabolic conditions or skin health, as well as in the synthesis of bioactive peptides or molecular interactions. Further research into its specific activities and interactions could open up new avenues for its application in healthcare, personal care, and biotechnology.

