Cas no 20725-03-5 (3,3',4',7-Tetrahydroxyflavanone)
3,3',4',7-Tetrahydroxyflavanone Chemical and Physical Properties
Names and Identifiers
-
- 4H-1-Benzopyran-4-one,2-(3,4-dihydroxyphenyl)-2,3-dihydro-3,7-dihydroxy-, (2R,3R)-rel-
- 4H-1-Benzopyran-4-one,2-(3,4-dihydroxyphenyl)-2,3-dihydro-3,7-dihydroxy-, trans-
- Flavanone,3,3',4',7-tetrahydroxy- (7CI,8CI)
- Fustin (6CI)
- (?à)-Fustin
- 2,3-Dihydrofisetin
- Dihydrofisetin
- NSC59264
- trans-(?à)-3,3',4',7-Tetrahydroxyflavanone
- Fustin
- FUSTIN(AS)
- 2,3-DIHYDROFISETH
- 3,3',4',7-tetrahydroxyflavanone
- 3',4',7-TRIHYDROXYFLAVANONOL
- 3,7,3',4'-tetrahydroxyflavanone
- 3,7,3',4'-tetrahydroxyflavone
- 5-Deoxydihydrouercetin
- [ "Dihydrofisetin" ]
- AKOS032948206
- (2R,3R)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxychroman-4-one
- (2R,3S)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-2,3-dihydro-4H-chromen-4-one
- Fustin (2R,3R)-form [MI]
- TRANS-(+/-)-3,3',4',7-TETRAHYDROXYFLAVANONE
- (2R,3R)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-2,3-dihydro-4H-1-benzopyran-4-one
- (+)-3,3',4',7-tetrahydroxyflavanone
- trans-2-(3,4-Dihydroxyphenyl)-2,3-dihydro-3,7-dihydroxy-4-benzopyrone
- C01378
- FUSTIN, (+/-)-
- 4H-1-Benzopyran-4-one,2-(3,4-dihydroxyphenyl)-2,3-dihydro-3,7-dihydroxy-,(2R,3R)-rel-
- DTXSID70871986
- CHEBI:228234
- Flavanone, 3,3',4',7-tetrahydroxy- (VAN)
- (2R,3R)-fustin
- 2,3-TRANS-FUSTIN
- (2R,3R)-2-(3,4-Dihydroxyphenyl)-2,3-dihydro-3,7-dihydroxy-4H-1-benzopyran-4-one
- UNII-4994C1X19A
- Fustin, (+)-
- 4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-2,3-dihydro-3,7-dihydroxy-, (2R,3R)-
- UNII-C308QR79UE
- SCHEMBL13640269
- (2R,3R)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-chroman-4-one
- (2R,3R)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-2,3-dihydrochromen-4-one
- 3,7,3',4'-Tetrahydroxy-flavanon
- 4382-36-9
- C308QR79UE
- Q5510352
- Ambap20725-03-5
- 4H-1-BENZOPYRAN-4-ONE, 2-(3,4-DIHYDROXYPHENYL)-2,3-DIHYDRO-3,7-DIHYDROXY-, (2R-TRANS)-
- fustin (2R,3R)-form
- Flavanone, 3,3',4',7-tetrahydroxy-(VAN)
- CHEBI:5202
- (2R-trans)-2-(3,4-dihydroxyphenyl)-2,3-dihydro-3,7-dihydroxy-4H-1-benzopyran-4-one
- (2R,3R)-3,7,3',4'-tetrahydroxyflavanone
- CHEMBL470267
- 4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-2,3-dihydro-3,7-dihydroxy-, trans-
- SureCN13640269
- CS-0143760
- (+)-trans-fustin
- NSC-59264
- 20725-03-5
- HY-N8376
- DTXSID401136309
- 4994C1X19A
- MFCD00075647
- 4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-2,3-dihydro-3,7-dihydroxy-, (2R,3R)-rel-
- FUSTIN [MI]
- NSC 59264
- (+/-)-Fustin
- Flavanone, 3,3',4',7-tetrahydroxy-, (+)-
- (2R,3R)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-2,3-dihydro-4H-chromen-4-one
- Tetrahydroxyflavanone
- (+)-2,3-dihydrofisetin
- (+)-Fustin
- AC1NSVLG
- EINECS 243-989-6
- FS-9541
- Flavanone, 3,3',4',7-tetrahydroxy-
- 2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-chroman-4-one
- SCHEMBL555237
- DTXSID801021299
- FNUPUYFWZXZMIE-UHFFFAOYSA-N
- Flavanone,3',4',7-tetrahydroxy-
- 2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-2,3-dihydrochromen-4-one
- 4H-1-Benzopyran-4-one,4-dihydroxyphenyl)-2,3-dihydro-3,7-dihydroxy-, trans-
- CHEMBL508731
- 2-(3,4-Dihydroxyphenyl)-2,3-dihydro-3,7-dihydroxy-4H-1-benzopyran-4-one
- 101849-13-2
- NS00050222
- FT-0773982
- DA-49257
- G77035
- FNUPUYFWZXZMIE-LSDHHAIUSA-N
- 3,3',4',7-Tetrahydroxyflavanone
-
- MDL: MFCD00075647
- Inchi: 1S/C15H12O6/c16-8-2-3-9-12(6-8)21-15(14(20)13(9)19)7-1-4-10(17)11(18)5-7/h1-6,14-18,20H/t14-,15+/m0/s1
- InChI Key: FNUPUYFWZXZMIE-LSDHHAIUSA-N
- SMILES: O1C2C=C(C=CC=2C([C@@H]([C@H]1C1C=CC(=C(C=1)O)O)O)=O)O
Computed Properties
- Exact Mass: 288.06300
- Monoisotopic Mass: 288.063388
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 4
- Hydrogen Bond Acceptor Count: 6
- Heavy Atom Count: 21
- Rotatable Bond Count: 1
- Complexity: 400
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 2
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 107
- XLogP3: 1.3
Experimental Properties
- Color/Form: Powder
- Density: 1.6±0.1 g/cm3
- Melting Point: 216-217°C
- Boiling Point: 644.2±55.0 °C at 760 mmHg
- Flash Point: 249.2±25.0 °C
- Refractive Index: 1.728
- PSA: 107.22000
- LogP: 1.48070
- Vapor Pressure: 0.0±2.0 mmHg at 25°C
3,3',4',7-Tetrahydroxyflavanone Security Information
- Signal Word:warning
- Hazard Statement: H303+H313+H333
- Warning Statement: P264+P280+P305+P351+P338+P337+P313
- Hazard Category Code: 36/37/38
- Safety Instruction: S26; S36
- Risk Phrases:R36/37/38
- Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
3,3',4',7-Tetrahydroxyflavanone Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | F20390-5mg |
Fustin |
20725-03-5 | ,HPLC≥95% | 5mg |
¥4640.0 | 2023-09-07 | |
| abcr | AB152006-5 mg |
3,7,3',4'-Tetrahydroxyflavanone |
20725-03-5 | 5 mg |
€326.40 | 2023-07-20 | ||
| TRC | T795753-1mg |
3,3',4',7-Tetrahydroxyflavanone |
20725-03-5 | 1mg |
$ 50.00 | 2022-06-02 | ||
| TRC | T795753-2mg |
3,3',4',7-Tetrahydroxyflavanone |
20725-03-5 | 2mg |
$ 65.00 | 2022-06-02 | ||
| TRC | T795753-10mg |
3,3',4',7-Tetrahydroxyflavanone |
20725-03-5 | 10mg |
$ 135.00 | 2022-06-02 | ||
| SHANG HAI TAO SHU Biotechnology Co., Ltd. | TN1653-1 mg |
Fustin |
20725-03-5 | 1mg |
¥3500.00 | 2022-04-26 | ||
| eNovation Chemicals LLC | K33089-5mg |
Fustin |
20725-03-5 | 98% | 5mg |
$585 | 2025-02-18 | |
| eNovation Chemicals LLC | K33089-10mg |
Fustin |
20725-03-5 | 98% | 10mg |
$1065 | 2025-02-18 | |
| TargetMol Chemicals | TN1653-1mg |
Fustin |
20725-03-5 | 1mg |
¥ 497 | 2024-07-20 | ||
| TargetMol Chemicals | TN1653-10mg |
Fustin |
20725-03-5 | 10mg |
¥ 2460 | 2024-07-20 |
3,3',4',7-Tetrahydroxyflavanone Related Literature
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1. Immediate biogenetic precursors of mopanols and peltogynolsJohanna P. van der Merwe,D. Ferreira,E. V. Brandt,D. G. Roux J. Chem. Soc. Chem. Commun. 1972 521
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2. Phytochemistry of the gum copal tree, Trachylobium verrucosum(gaertn.) oliv. The first natural α-hydroxychalcone and 2,3-cis- and 2,3-trans-3-methoxyflavanonesDaneel Ferreira,Johanna P. van der Merwe,David G. Roux J. Chem. Soc. Perkin Trans. 1 1974 1492
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3. Photochemical deoxygenation of an α-ketol: the dihydroflavonol–flavanone conversionJan H. van der Westhuizen,Daneel Ferreira,David G. Roux J. Chem. Soc. Perkin Trans. 1 1980 1003
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4. Metabolites from the purple heartwood of Mimosoideae I, Acacia peuce F. Muell: the first natural 2,3-cis-peltogynoidsEdward V. Brandt,David G. Roux J. Chem. Soc. Perkin Trans. 1 1979 777
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5. Flavonoid synthesis based on photolysis of flavan-3-ols, 3-hydroxyflavanones, and 2-benzylbenzofuranonesTheunis G. Fourie,Daneel Ferreira,David G. Roux J. Chem. Soc. Perkin Trans. 1 1977 125
Additional information on 3,3',4',7-Tetrahydroxyflavanone
Exploring the Potential of 3,3',4',7-Tetrahydroxyflavanone (CAS No. 20725-03-5): A Comprehensive Overview
3,3',4',7-Tetrahydroxyflavanone, a naturally occurring flavonoid, has garnered significant attention in recent years due to its diverse biological activities and potential health benefits. With the growing interest in plant-derived compounds for wellness and therapeutic applications, this compound stands out as a promising candidate. Its CAS number 20725-03-5 serves as a unique identifier in scientific literature and commercial databases, ensuring accurate referencing for researchers and industry professionals alike.
The molecular structure of 3,3',4',7-Tetrahydroxyflavanone features four hydroxyl groups attached to the flavanone backbone, contributing to its antioxidant properties. This structural configuration makes it particularly interesting for studies involving oxidative stress-related conditions, a topic that has seen increased search volume in health and nutrition forums. Many users searching for "natural antioxidants for cellular health" or "flavonoids for inflammation" would find this compound relevant to their queries.
Recent studies have highlighted the potential of 3,3',4',7-Tetrahydroxyflavanone in supporting cardiovascular health, with particular attention to its vasorelaxant effects. This aligns with current health trends focusing on natural approaches to maintaining healthy blood pressure levels. The compound's ability to modulate certain enzymatic pathways has also made it a subject of interest in metabolic health research, addressing common search queries about "natural compounds for metabolic support."
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From a commercial perspective, the market for 3,3',4',7-Tetrahydroxyflavanone has seen steady growth, particularly in the nutraceutical and cosmeceutical sectors. Quality parameters such as purity levels (typically ≥95% for research applications) and sourcing methods (often derived from citrus or other plant sources) are key considerations for buyers. These specifications frequently appear in procurement-related searches by industry professionals evaluating potential suppliers.
Ongoing research continues to uncover new potential applications for 3,3',4',7-Tetrahydroxyflavanone, including its role in neuroprotection and cognitive health. This aligns with growing consumer interest in nootropic compounds and natural approaches to brain health, as evidenced by search trends for "flavonoids for memory support." The compound's ability to cross the blood-brain barrier in experimental models makes it particularly intriguing for these applications.
Standardization and analytical methods for 3,3',4',7-Tetrahydroxyflavanone quantification have improved significantly, with HPLC-UV and LC-MS/MS being the most commonly employed techniques. These methodological details are frequently searched by quality control professionals and researchers working with flavonoid analysis, highlighting the importance of including such technical information in comprehensive profiles of this compound.
As sustainability becomes increasingly important in ingredient sourcing, the ecological aspects of 3,3',4',7-Tetrahydroxyflavanone production have come into focus. Many users searching for "sustainable flavonoid sources" or "eco-friendly plant extracts" would find information about this compound relevant. Current production methods emphasize green extraction techniques and utilization of agricultural byproducts, aligning with circular economy principles.
The safety profile of 3,3',4',7-Tetrahydroxyflavanone has been extensively studied, with research indicating good tolerability at physiologically relevant concentrations. This information addresses common consumer concerns reflected in search queries like "are flavonoids safe for long-term use" or "potential side effects of plant compounds." Comprehensive toxicological assessments continue to support its potential for various applications.
Looking forward, the research landscape for 3,3',4',7-Tetrahydroxyflavanone appears promising, with several clinical trials underway to evaluate its efficacy in human applications. These developments respond to the growing demand for evidence-based natural compounds, a trend clearly visible in search engine data showing increased queries for "clinical studies on flavonoids" and "scientifically validated plant extracts."
For researchers and product developers working with 3,3',4',7-Tetrahydroxyflavanone, proper storage conditions (typically -20°C protected from light) and handling procedures are essential considerations. These practical details often appear in technical searches by laboratory personnel, underscoring the importance of including such information in comprehensive compound profiles.
The intellectual property landscape surrounding 3,3',4',7-Tetrahydroxyflavanone has become increasingly active, with patents covering various formulations and applications. This commercial aspect is particularly relevant for industry professionals searching for "flavonoid patents" or "novel delivery systems for plant compounds," indicating the compound's growing importance in product development.
In conclusion, 3,3',4',7-Tetrahydroxyflavanone (CAS No. 20725-03-5) represents a fascinating intersection of traditional plant medicine and modern scientific research. Its diverse biological activities and multiple potential applications make it a compound of significant interest across various fields, from nutrition to cosmetics to therapeutic development. As research continues to uncover its mechanisms and benefits, this flavonoid is poised to remain a focus of scientific and commercial attention in the coming years.