Cas no 469-32-9 (Hamamelitannin)
Hamamelitannin Chemical and Physical Properties
Names and Identifiers
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- D-Ribose,2-C-[[(3,4,5-trihydroxybenzoyl)oxy]methyl]-, 5-(3,4,5-trihydroxybenzoate)
- Root of Chinese Witchhazel
- HAMAMELITANNIN(P)
- HAMAMELITANNIN
- 2,3-Digalloylglucose
- 2',5-DigalloylhaMaMelofuranose
- 2',5-digalloylhamamelose
- hamamelitanin
- HAMAMELOFURANOSE 2',5-DIGALLATE
- O5-Galloyl-2-galloyloxymethyl-D-ribose
- 2-C-(Hydroxymethyl)-D-ribofuranose 2′,5-digallate
- Hamamelofuranose 2′,5-digallate
- NSC77009
- [3,4,5-trihydroxy-4-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxolan-2-yl]methyl 3,4,5-trihydroxybenzoate
- (2,3,4-trihydroxy-5-{[(3,4,5-trihydroxyphenyl)carbonyloxy]methyl}oxolan-3-yl)methyl 3,4,5-trihydroxybenzoate
- ((2S,3S,4S)-3,4,5-trihydroxytetrahydrofuran-2,4-diyl)bis(methylene) bis(3,4,5-trihydroxybenzoate)
- MFCD33023081
- 469-32-9
- CHEBI:191119
- Q15632711
- Hamamelofuranose 2'5'-digallate
- Hamamelofuranose2,5-digallate
- [(2S,3S,4S)-3,4,5-trihydroxy-4-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxolan-2-yl]methyl 3,4,5-trihydroxybenzoate
- CHEMBL465414
- FS-7252
- DTXSID10963692
- FT-0632174
- 5-O-(3,4,5-Trihydroxybenzoyl)-2-C-{[(3,4,5-trihydroxybenzoyl)oxy]methyl}pentose
- EINECS 207-416-3
- Gallic acid, 21,5-diester with 2-C-(hydroxymethyl)-D-ribose
- NS00043231
- HAMAMELITANNIN [MI]
- 2-C-((Galloyloxy)methyl)-D-ribose 5-gallate
- 2',5-DI-O-GALLOYL-D-HAMAMELOSE
- hamamelitannin (open form)
- CS-0032127
- UNII-Z4320A2K26
- HY-N4117
- Q27294967
- Z4320A2K26
- AKOS040760441
- D-RIBOSE, 2-C-(((3,4,5-TRIHYDROXYBENZOYL)OXY)METHYL)-, 5-(3,4,5-TRIHYDROXYBENZOATE)
- 2',5'-Di-O-galloyl D-hamamelose
- [(2R,3R,4R)-3,4,5-trihydroxy-4-[(3,4,5-trihydroxybenzoyl)oxymethyl]tetrahydrofuran-2-yl]methyl 3,4,5-trihydroxybenzoate
- Hamamelitannin, >=98.0% (HPLC)
- SCHEMBL934789
- CHEMBL491592
- A827115
- 2-C-(Hydroxymethyl)-D-ribofuranose 2',5-digallate
- BDBM50259992
- [(2R,3R,4R)-3,4,5-trihydroxy-4-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxolan-2-yl]methyl 3,4,5-trihydroxybenzoate
- SCHEMBL14339420
- NSC-77009
- D-Ribose, 2-C-[[(3,4,5-trihydroxybenzoyl)oxy]methyl]-, 5-(3,4,5-trihydroxybenzoate); Hamamelitannin (6CI,7CI); Ribose, 2-C-(hydroxymethyl)-, 21,5-digallate, D- (8CI); Gallic acid, 21,5-diester with 2-C-(hydroxymethyl)-D-ribose (8CI); 2',5-Di-O-galloyl-D-hamamelose
- FEPAFOYQTIEEIS-WZKFEGCESA-N
- Hamamelitannin
-
- MDL: MFCD33023081
- Inchi: 1S/C20H20O14/c21-9-1-7(2-10(22)14(9)25)17(28)32-5-13-16(27)20(31,19(30)34-13)6-33-18(29)8-3-11(23)15(26)12(24)4-8/h1-4,13,16,19,21-27,30-31H,5-6H2/t13-,16-,19?,20-/m0/s1
- InChI Key: FEPAFOYQTIEEIS-WZKFEGCESA-N
- SMILES: O1C([C@](COC(C2C=C(C(=C(C=2)O)O)O)=O)([C@H]([C@@H]1COC(C1C=C(C(=C(C=1)O)O)O)=O)O)O)O
Computed Properties
- Exact Mass: 484.08500
- Monoisotopic Mass: 484.08530531 g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 9
- Hydrogen Bond Acceptor Count: 14
- Heavy Atom Count: 34
- Rotatable Bond Count: 8
- Complexity: 710
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 3
- Undefined Atom Stereocenter Count : 1
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 244
- Molecular Weight: 484.4
- XLogP3: -1.1
Experimental Properties
- Density: 1.771±0.06 g/cm3 (20 oC 760 Torr),
- Melting Point: 145-147 oC
- Boiling Point: 947.5°Cat760mmHg
- Flash Point: 331°C
- Refractive Index: 1.745
- Solubility: Slightly soluble (6.3 g/l) (25 o C),
- PSA: 243.90000
- LogP: -1.25680
- Specific Rotation: D19 +32.6° (c = 1.5)
Hamamelitannin Security Information
- Hazardous Material transportation number:NONH for all modes of transport
- WGK Germany:3
- FLUKA BRAND F CODES:3-10-21
- Storage Condition:2-8°C
Hamamelitannin Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| abcr | AB166376-20 mg |
Hamamelitannin, 95%; . |
469-32-9 | 95% | 20 mg |
€388.80 | 2023-07-20 | |
| Chengdu Biopurify Phytochemicals Ltd | BP0695-10mg |
Hamamelitannin |
469-32-9 | 98% | 10mg |
$290 | 2023-09-20 | |
| Chengdu Biopurify Phytochemicals Ltd | BP0695-20mg |
Hamamelitannin |
469-32-9 | 98% | 20mg |
$450 | 2023-09-20 | |
| ChemScence | CS-0032127-1mg |
Hamamelitannin |
469-32-9 | 1mg |
$120.0 | 2022-04-27 | ||
| ChemScence | CS-0032127-5mg |
Hamamelitannin |
469-32-9 | 5mg |
$300.0 | 2022-04-27 | ||
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | H99270-10mg |
HAMAMELITANNIN |
469-32-9 | ,HPLC≥95% | 10mg |
¥2468.0 | 2023-09-07 | |
| SHANG HAI TAO SHU Biotechnology Co., Ltd. | TN1722-1 mg |
Hamamelitannin |
469-32-9 | 1mg |
¥987.00 | 2022-04-26 | ||
| MedChemExpress | HY-N4117-1mg |
Hamamelitannin |
469-32-9 | 99.43% | 1mg |
¥1200 | 2025-04-16 | |
| MedChemExpress | HY-N4117-5mg |
Hamamelitannin |
469-32-9 | 99.43% | 5mg |
¥2500 | 2025-04-16 | |
| TRC | H175460-0.5mg |
Hamamelitannin |
469-32-9 | 0.5mg |
$ 50.00 | 2022-06-04 |
Hamamelitannin Suppliers
Hamamelitannin Related Literature
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Roberta J. Melander,Akash K. Basak,Christian Melander Nat. Prod. Rep. 2020 37 1454
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Sivasamy Sethupathy,Loganathan Vigneshwari,Alaguvel Valliammai,Krishnaswamy Balamurugan,Shunmugiah Karutha Pandian RSC Adv. 2017 7 23392
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Junwei Cao,Yao Zhang,Lin Han,Shanbo Zhang,Xuchang Duan,Lijun Sun,Min Wang Food Funct. 2020 11 3838
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Xi Li,Biao Wu,Hao Chen,Kaihui Nan,Yingying Jin,Lin Sun,Bailiang Wang J. Mater. Chem. B 2018 6 4274
-
Gerard D. Wright Nat. Prod. Rep. 2017 34 694
Additional information on Hamamelitannin
Hamamelitannin (CAS No. 469-32-9): A Comprehensive Overview of Its Properties, Applications, and Market Trends
Hamamelitannin (CAS No. 469-32-9) is a naturally occurring hydrolyzable tannin derived from the bark and leaves of the witch hazel plant (Hamamelis virginiana). This bioactive compound has garnered significant attention in recent years due to its potent antioxidant, anti-inflammatory, and skin-protective properties. As consumer demand for natural skincare ingredients and plant-based therapeutics continues to rise, Hamamelitannin has emerged as a key player in the cosmeceutical and pharmaceutical industries.
The chemical structure of Hamamelitannin consists of a glucose core esterified with two gallic acid units, making it a member of the ellagitannin family. This unique configuration contributes to its remarkable biological activities, including free radical scavenging and metal chelation. Recent studies published in Journal of Natural Products highlight its superior antioxidant capacity compared to many synthetic alternatives, making it particularly valuable for anti-aging formulations and UV protection products.
In the cosmetics industry, Hamamelitannin is increasingly incorporated into serums, creams, and toners targeting sensitive skin and rosacea-prone complexions. Its ability to strengthen capillary walls and reduce redness aligns perfectly with current consumer searches for "natural remedies for facial redness" and "plant-based solutions for sensitive skin". Leading skincare brands now feature witch hazel extracts rich in Hamamelitannin as their star ingredients, capitalizing on the growing clean beauty movement.
Beyond skincare, research suggests promising applications of Hamamelitannin in wound healing and oral care products. Its astringent properties make it effective in mouthwashes for gum health, addressing popular consumer concerns about "natural alternatives to chemical mouthwashes". The compound's antibacterial activity against oral pathogens has been documented in several peer-reviewed studies, supporting its use in holistic dental care formulations.
The global market for Hamamelitannin is experiencing steady growth, driven by increasing awareness of its multifunctional benefits. Market analysis reveals particular demand in North America and Europe, where consumers actively search for "clinical studies on witch hazel tannins" and "evidence-based natural ingredients". Suppliers are responding with standardized extracts containing precise Hamamelitannin concentrations to meet formulation requirements for cosmetic chemists and nutraceutical developers.
From a sustainability perspective, Hamamelitannin production aligns with eco-conscious manufacturing trends. The witch hazel plant requires minimal pesticides and thrives in diverse climates, making it an attractive source for green chemistry applications. This environmental profile resonates with consumers searching for "sustainable bioactive compounds" and "ethically sourced plant extracts".
Ongoing research continues to uncover new potential for Hamamelitannin, including investigations into its metabolic effects and possible role in gut health. As scientific understanding expands, we can anticipate broader applications of this versatile compound across functional foods, dietary supplements, and medical devices. The future looks bright for Hamamelitannin as both consumers and researchers increasingly recognize its value in health and wellness applications.