9,10-didehydro-6-methyl-8-hydroxymethylergoline
Lysergol
CAS: 602-85-7
Molecular Formula: C16H18N2O
9,10-didehydro-6-methyl-8-hydroxymethylergoline - Names and Identifiers
9,10-didehydro-6-methyl-8-hydroxymethylergoline - Physico-chemical Properties
| Molecular Formula | C16H18N2O |
| Molar Mass | 254.33 |
| Density | 1.0398 (rough estimate) |
| Melting Point | 248°C |
| Boling Point | 397.54°C (rough estimate) |
| pKa | 14.61±0.10(Predicted) |
| Storage Condition | 2-8℃ |
| Refractive Index | 1.6240 (estimate) |
9,10-didehydro-6-methyl-8-hydroxymethylergoline - Risk and Safety
| Risk Codes | R26/27/28 - Very toxic by inhalation, in contact with skin and if swallowed. R36/37/38 - Irritating to eyes, respiratory system and skin. R25 - Toxic if swallowed |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) S36/37 - Wear suitable protective clothing and gloves. |
| UN IDs | 1544 |
| Hazard Class | 6.1(a) |
| Packing Group | II |
9,10-didehydro-6-methyl-8-hydroxymethylergoline - Reference Information
| Use | ergol is an ergot alkaloid, when used in combination with the antibiotic nalidixic acid, can effectively inhibit E. Coli. It also maintains its potential to act on 5-HT1/2 receptors and alpha1-adrenergic receptors, thereby acting as a neuropsychiatric drug. |
| legitimacy | ergosterol is an alkaloid of the ergotoxine family, and in some fungi (mostly in Claviceps) and the plants of the petaceae family (spinaceae) are present as minor components, including Rivea corymbosa (ololiuhqui), the hallucinogenic seeds of Argyreia nervosa (Hawaii rose), and sweet potatoes. Ergot alcohol is not a controlled substance in the United States. Its possession and sale is also legal under the United States federal simulation Act because it has no known pharmacological action or relationship to the precursor of LSD (a controlled substance). However, ergot alcohol is an intermediate in the manufacture of certain ergot drugs, such as nicergoline. Ergol can be synthesized using a tandem reaction with a piperidine skeleton and rhodium-catalyzed [32] cyclization in the late indole formation. |
Last Update：2024-04-09 02:00:12
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