Vincamine
Vincamine (CAS: 1617-90-9), with the molecular formula C21H26N2O3 and a molecular weight of 354.44 g/mol, is a naturally occurring indole alkaloid. It is recognised for its vasodilatory and neuroprotective properties. Vincamine finds application in research settings, particularly in studies related to cerebrovascular health and neurological functions. Its specific chemical structure makes it a valuable compound for investigations in organic synthesis and cell biology.
Cerebrovascular Research
Vincamine is investigated for its potential effects on blood flow in the brain, making it a subject of study in cerebrovascular research.
Neuroprotection Studies
This alkaloid is used in research to explore its neuroprotective capabilities, contributing to the understanding of brain cell resilience.
Chemical Synthesis
As a complex alkaloid, Vincamine serves as a building block or reference compound in advanced organic synthesis and medicinal chemistry.
Cell Biology Investigations
Vincamine is employed in cell biology research to study its impact on cellular processes and mechanisms, particularly within neural tissues.
| Molecular weight | 354.44 |
|---|---|
| Empirical formula | C21H26N2O3 |
| Assay | 98% |
| Optical activity | [α]23/D +42.8°, c = 1 in pyridine |
| Melting point | 232 °C (dec.)(lit.) |
Hazard statements
- H302Harmful if swallowed
| Protective equipment | dust mask type N95 (US), Eyeshields, Gloves |
|---|---|
| Water hazard class (WGK, DE) | 3 |
| Hazard codes (EU) | Xn |
| Risk statements (R) | 22 |
| Safety statements (S) | 36 |
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is Vincamine used for?
+
Vincamine is primarily used in research, particularly for studying cerebrovascular health, neuroprotection, and as a compound in chemical synthesis and cell biology investigations.
What are the CAS number and formula for Vincamine?
+
The CAS number for Vincamine is 1617-90-9, and its molecular formula is C21H26N2O3.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies Vincamine with an assay of 98%. This product is intended for research and technical use and is not represented as USP, BP, EP, or other pharmacopoeial grades.
How should Vincamine be handled safely?
+
Vincamine is classified as harmful if swallowed (H302). Recommended personal protective equipment includes a dust mask (type N95 US), eyeshields, and gloves. Handle in a well-ventilated area and avoid dust formation.
Is Vincamine a controlled substance?
+
The provided data does not indicate that Vincamine is a controlled substance.
How is Vincamine packaged and shipped?
+
Vincamine is carefully packaged to ensure stability during transport and is exported globally by Tech Serve Solutions.
How can I request a quote or sample of Vincamine?
+
To request a quote or sample of Vincamine, please contact the Tech Serve Solutions sales team via our website or designated contact channels.
▶ Related products
1-(2-Fluorobenzyl)piperazine
C11H15FN2
Chemical Synthesis
1-(2-Fluorophenyl)biguanide hydrochloride
Chemical Synthesis
1-(2-Fluorophenyl)cyclopropanecarboxylic acid
C10H9FO2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine
C10H13FN2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine monohydrochloride
C10H13FN2 · HCl
Chemical Synthesis
1-(2-Furoyl)-1H-benzotriazole
C11H7N3O2
Chemical Synthesis
1-(2-Furoyl)piperazine
C9H12N2O2
Chemical Synthesis
1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione
Chemical Synthesis
▶ Explore more
3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis
3-Methyl-1,5-pentanediol
Chemical Synthesis
3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis