- Scopoletin
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- $30.00
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2026-04-22
- CAS:92-61-5
- Purity: 97.06%
- Supply Ability: 10g
- Scopoletin
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2026-02-02
- CAS:92-61-5
- Min. Order: 5mg
- Purity: 99%HPLC
- Supply Ability: 2000tons
- Scopoletin
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-
2024-04-12
- CAS:92-61-5
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 2000ton
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| | Scopoletin Basic information |
| | Scopoletin Chemical Properties |
| Melting point | 203-205 °C (lit.) | | Boiling point | 288.14°C (rough estimate) | | density | 1.2932 (rough estimate) | | refractive index | 1.5430 (estimate) | | storage temp. | 2-8°C | | solubility | Chloroform (Sightly, Heated), Ethyl Acetate (Slightly, Heated), Methanol (Slightly, Heated) | | pka | 7.91±0.20(Predicted) | | form | Crystalline Powder | | color | Beige | | Water Solubility | Slightly soluble | | Merck | 14,8408 | | BRN | 156296 | | InChI | 1S/C10H8O4/c1-13-9-4-6-2-3-10(12)14-8(6)5-7(9)11/h2-5,11H,1H3 | | InChIKey | RODXRVNMMDRFIK-UHFFFAOYSA-N | | SMILES | COc1cc2C=CC(=O)Oc2cc1O | | LogP | 1.280 (est) | | CAS DataBase Reference | 92-61-5(CAS DataBase Reference) | | NIST Chemistry Reference | 7-Hydroxy-6-methoxy-2h-1-benzopyran-2-one(92-61-5) | | EPA Substance Registry System | Scopoletin (92-61-5) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36-37/39 | | WGK Germany | 2 | | RTECS | GN6930000 | | HS Code | 29322090 | | Storage Class | 11 - Combustible Solids |
| | Scopoletin Usage And Synthesis |
| Chemical Properties | Crystalline Solid | | Uses | Scopoletin is the aglucone of Scopolin. Used for cosmetics, topical formulations, and foods. Dyes and metabolites. | | Definition | ChEBI: A hydroxycoumarin that is umbelliferone bearing a methoxy substituent at position 6. | | benefits | Scopoletin is a coumarin synthesized by diverse medicinal and edible plants, which plays a vital role as a therapeutic and chemopreventive agent in the treatment of a variety of diseases. Scopoletin is indicated to have antimicrobial, anticancer, anti-inflammation, anti-angiogenesis, anti-oxidation, antidiabetic, antihypertensive, hepatoprotective, and neuroprotective properties and immunomodulatory effects in both in vitro and in vivo experimental trials. In addition, it is an inhibitor of various enzymes, including choline acetyltransferase, acetylcholinesterase, and monoamine oxidase. | | Synthesis Reference(s) | The Journal of Organic Chemistry, 27, p. 3083, 1962 DOI: 10.1021/jo01056a023 | | General Description | Scopoletin is a coumarin compound and pharmacologically active chemical that is found in various plant species. | | Biochem/physiol Actions | Scopoletin significantly increases activity of lipoprotein lipase in adipocytes by promoting transcription of the LPL gene. It also partially reverses inhibition of LPL by TNF-α. | | Purification Methods | Crystallise it from water, acetic acid or *C6H6/MeOH. It is dimorphic with a second m at 193-195o. It sublimes at 120-130o/12mm. [Beilstein 18 H 99, 18 I 348, 18 II 68, 18 III/IV 1323, 18/3 V 203.] |
| | Scopoletin Preparation Products And Raw materials |
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