Strychnine TCI S0249

Chemical Identity

CAS No.: 57-24-9
PubChem: CID 441071·SID 87575778
Formula: C21H22N2O2
Molecular weight: 334.4 g/mol
Purity: >98.0%(HPLC)(T)
Reference databases: ChEBI·ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (4aR,5aS,8aR,13aS,15aS,15bR)-4a,5,5a,7,8,13a,15,15a,15b,16-decahydro-2H-4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-14-one
SMILES: C1CN2CC3=CCO[C@H]4CC(=O)N5[C@H]6[C@H]4[C@H]3C[C@H]2[C@@]61C7=CC=CC=C75
InChIKey: QMGVPVSNSZLJIA-FVWCLLPLSA-N

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Strychnine is a chemical compound widely used in various chemical experiments and organic synthesis processes. As a complex alkaloid, it plays a significant role in chiral resolution and asymmetric synthesis, where its unique molecular structure enables the separation of enantiomers. This compound is essential for researchers aiming to achieve specific enantiomeric activity in their products, which is crucial in pharmaceutical and medicinal chemistry. Its presence in laboratory settings allows for the development of more precise and effective drug formulations.

Strychnine is valued for its chemical stability under controlled conditions, although it is highly sensitive to moisture and air exposure. Its complex molecular structure allows it to interact effectively with various reagents, making it a preferred choice for chiral resolution applications. The compound's ability to participate in high-resolution chiral reactions enhances its utility in advanced synthetic processes. Its unique properties make it a reliable reagent for experiments requiring precise stereochemical control.

In Indonesian laboratories, strychnine is commonly used in organic chemistry research, particularly in studies involving molecular structure and reaction mechanisms. It is a key component in experiments that require chiral resolution, contributing to the development of new pharmaceutical compounds. Its application in both academic and industrial research settings underscores its importance in the field of chemical synthesis.

TCI brochures (PDF)

Reagents for Preparing Animal Disease Models 2024-09-13 · p. 1
Traditional Medicine/Crude Medicine Research Reagents 2024-09-11 · p. 1
Chiral Auxiliaries and Optical Resolving Agents 2025-06-17 · p. 5
Alkaloids 2025-10-10 · p. 6
Plant Research Reagents 2026-02-24 · p. 8
Phytochemicals 2025-12-17 · p. 4

Related TCI products

Chiral Resolution Experiments: Strychnine is ideal for chiral resolution due to its ability to interact with enantiomers, enabling the separation of complex molecular structures.
Organic Synthesis Research: This compound supports the creation of enantiomerically pure compounds, which is essential in drug development and pharmaceutical studies.
Molecular Structure Analysis: Its complex structure makes it valuable for studying molecular interactions and reaction mechanisms in chemical research.
Asymmetric Catalysis Studies: Strychnine's unique properties aid in the development of asymmetric catalysts, enhancing the efficiency of synthetic processes.
Pharmaceutical Compound Development: It is used to achieve specific enantiomeric activity, which is critical in the formulation of effective and safe medicinal products.

Brand	TCI
CAS number	57-24-9
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Resolution Reagents
Pack sizes	—
Physical form	—
Storage	Store in a cool, dry place away from moisture and air exposure.

Strychnine should be stored in a cool, dry environment to maintain its chemical stability. It is essential to use airtight containers to prevent exposure to moisture and air, which can degrade the compound. Due to its sensitivity, it should be handled in a controlled laboratory setting with appropriate safety measures. Avoid direct contact with skin and inhalation of vapors. Keep the compound away from heat sources and incompatible materials. Regular monitoring of storage conditions ensures the integrity of the material for experimental use. Proper labeling and secure storage are recommended to prevent accidental exposure and contamination.

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