- Scopoletin
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- $0.00 / 25kg
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2024-04-12
- CAS:92-61-5
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 2000ton
- Scopoletin
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- $0.00 / 20mg
-
2023-02-24
- CAS:92-61-5
- Min. Order: 5mg
- Purity: ≥98%(HPLC)
- Supply Ability: 10 g
- Scopoletin
-
- $0.00 / 20mg
-
2023-02-24
- CAS:92-61-5
- Min. Order: 5mg
- Purity: Analytical Standard
- Supply Ability: 10 g
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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 | | InChIKey | RODXRVNMMDRFIK-UHFFFAOYSA-N | | 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 |
| | Scopoletin Usage And Synthesis |
| Chemical Properties | Crystalline Solid | | Uses | Scopoletin can be used for cosmetics, topical formulations, and foods. | | 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. | | 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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