Cas no 31524-62-6 (Isobavachin)
Isobavachin Chemical and Physical Properties
Names and Identifiers
-
- Isobavachin
- 4H-1-Benzopyran-4-one,2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-, (2S)-
- 4H-1-Benzopyran-4-one,2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-, (2...
- (2S)-2,3-Dihydro-7-hydroxy-2-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)- 4H-1-benzopyran-4-one
- [ "4'", "7-Dihydroxy-8-prenylflavanone" ]
- 4'
- DTXSID20953509
- AKOS040757105
- CS-0009788
- CCG-267745
- CHEMBL491534
- s9256
- 7-Hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-en-1-yl)-2,3-dihydro-4H-1-benzopyran-4-one
- HY-N0762
- 31524-62-6
- MS-24834
- HMS3886L20
- AC-35022
- (2S)-7-hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one
- CHEBI:186172
- DA-54398
- (2S)-7-HYDROXY-2-(4-HYDROXYPHENYL)-8-(3-METHYLBUT-2-EN-1-YL)-2,3-DIHYDRO-1-BENZOPYRAN-4-ONE
- GLXC-01646
- 4',7-dihydroxy-8-prenylflavanone
-
- Inchi： 1S/C20H20O4/c1-12(2)3-8-15-17(22)10-9-16-18(23)11-19(24-20(15)16)13-4-6-14(21)7-5-13/h3-7,9-10,19,21-22H,8,11H2,1-2H3/t19-/m0/s1
- InChI Key： KYFBXCHUXFKMGQ-IBGZPJMESA-N
- SMILES： O1C2C(=C(C=CC=2C(C[C@H]1C1C=CC(=CC=1)O)=O)O)C/C=C(\C)/C
Computed Properties
- Exact Mass: 324.1362
- Monoisotopic Mass: 324.136
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 24
- Rotatable Bond Count: 3
- Complexity: 474
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 1
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 66.8A^2
- Molecular Weight: 324.4
- XLogP3: 4.1
Experimental Properties
- Color/Form: Powder
- Density: 1.244
- Melting Point: 187-188 oC
- Boiling Point: 558.3°C at 760 mmHg
- Flash Point: 202.1°C
- Refractive Index: 1.621
- PSA: 66.76
- LogP: 4.31300
- Vapor Pressure: No data available
Isobavachin Security Information
- Signal Word：warning
- Hazard Statement： H303+H313+H333
- Warning Statement： P264+P280+P305+P351+P338+P337+P313
- Safety Instruction： H303+H313+H333
- Storage Condition：Store at 4 ° C, -4 ° C is better
Isobavachin Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| ChemFaces | CFN98400-20mg |
Isobavachin |
31524-62-6 | >=98% | 20mg |
$188 | 2021-07-22 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | QL626-20mg |
Isobavachin |
31524-62-6 | HPLC≥95+% | 20mg |
1501CNY | 2021-05-08 | |
| TRC | I315240-1mg |
Isobavachin |
31524-62-6 | 1mg |
$161.00 | 2023-05-18 | ||
| TRC | I315240-5mg |
Isobavachin |
31524-62-6 | 5mg |
$655.00 | 2023-05-18 | ||
| TRC | I315240-10mg |
Isobavachin |
31524-62-6 | 10mg |
$1263.00 | 2023-05-18 | ||
| Chengdu Biopurify Phytochemicals Ltd | BP0774-20mg |
Isobavachin |
31524-62-6 | 98% | 20mg |
$75 | 2023-09-20 | |
| Chengdu Biopurify Phytochemicals Ltd | BP0774-100mg |
Isobavachin |
31524-62-6 | 98% | 100mg |
$260 | 2023-09-20 | |
| DC Chemicals | DCZ-290-20 mg |
Isobavachin |
31524-62-6 | >98% | 20mg |
$380.0 | 2022-02-28 | |
| MedChemExpress | HY-N0762-5mg |
Isobavachin |
31524-62-6 | 99.90% | 5mg |
￥800 | 2024-07-21 | |
| MedChemExpress | HY-N0762-10mg |
Isobavachin |
31524-62-6 | 99.90% | 10mg |
￥1300 | 2024-07-21 |
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Isobavachin Related Literature
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Lu Liu,Hongsu Wang,Li Lin,Yawen Gao,Xiaodi Niu Food Funct. 2022 13 4032
Additional information on Isobavachin
Exploring Isobavachin (CAS No. 31524-62-6): A Comprehensive Guide to Its Properties and Applications
Isobavachin (CAS No. 31524-62-6) is a naturally occurring flavonoid compound derived from plants such as Psoralea corylifolia, commonly known as Babchi. This bioactive molecule has garnered significant attention in recent years due to its potential health benefits, particularly in the fields of anti-aging, skin care, and neuroprotection. As consumers increasingly seek natural alternatives to synthetic compounds, Isobavachin has emerged as a promising candidate for cosmeceutical and nutraceutical applications.
The chemical structure of Isobavachin features a chalcone backbone, which contributes to its antioxidant and anti-inflammatory properties. Researchers have identified its ability to scavenge free radicals, a key factor in addressing oxidative stress—a hot topic in modern health discussions. With the growing interest in holistic wellness, many users search for terms like "Isobavachin benefits" or "how does Isobavachin work," reflecting the public's curiosity about its mechanisms.
In the realm of dermatology, Isobavachin has shown potential in promoting collagen synthesis and reducing hyperpigmentation. These properties align with current trends in clean beauty and skin-brightening solutions. Studies suggest it may inhibit tyrosinase activity, making it relevant for those searching "natural skin whitening agents" or "plant-based melanin inhibitors." Its low cytotoxicity further enhances its appeal for topical formulations.
Beyond skincare, Isobavachin exhibits neuroprotective effects that have sparked interest in cognitive health applications. Preliminary research indicates potential in modulating neurotransmitter systems, connecting to popular searches about natural nootropics and brain-boosting supplements. The compound's ability to cross the blood-brain barrier makes it particularly noteworthy in this context.
From a pharmacological perspective, Isobavachin demonstrates multitarget activity, interacting with various biological pathways. This characteristic has led to investigations into its potential role in metabolic disorders and immune modulation—topics frequently searched alongside terms like "natural anti-diabetic compounds." Its structure-activity relationship continues to be an area of active research in medicinal chemistry.
The extraction and purification of Isobavachin present interesting challenges for phytochemistry professionals. Advanced techniques such as high-performance liquid chromatography (HPLC) are often employed to isolate this compound, addressing common queries about "how to extract Isobavachin" or "Isobavachin purity standards." The compound's stability profile under different pH conditions is another technical aspect frequently discussed in research circles.
In the supplement industry, Isobavachin is increasingly incorporated into formulations targeting longevity and cellular health. This aligns with the surge in searches for "bioactive flavonoids for healthspan" and "plant compounds for healthy aging." The compound's synergistic effects with other phytonutrients make it particularly valuable in multi-ingredient supplements.
Quality control remains paramount when working with Isobavachin, with analytical methods focusing on its isomeric purity and quantification. These technical aspects respond to professional searches about "Isobavachin analytical methods" or "standardization of flavonoid extracts." The compound's spectral characteristics, including its UV-Vis absorption maxima, serve as important identification markers.
As research continues, Isobavachin stands at the intersection of traditional medicine and modern science. Its diverse biological activities make it relevant to multiple disciplines, from cosmetic science to pharmacognosy. With increasing consumer awareness about plant-derived actives, this compound is poised to remain a subject of scientific and commercial interest in coming years.
