Psoralidin TCI P2605

Chemical Identity

CAS No.: 18642-23-4
PubChem: CID 5281806·SID 354335704
Formula: C20H16O5
Molecular weight: 336.3 g/mol
Purity: >98.0%(HPLC)
Reference databases: ChEBI·ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3,9-dihydroxy-2-(3-methylbut-2-enyl)-[1]benzofuro[3,2-c]chromen-6-one
SMILES: CC(=CCC1=CC2=C(C=C1O)OC(=O)C3=C2OC4=C3C=CC(=C4)O)C
InChIKey: YABIJLLNNFURIJ-UHFFFAOYSA-N

Rp 13.568.100,00

~~Rp 9.503.550,00~~ Rp 13.568.100,00

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Psoralidin, with CAS number 18642-23-4, is a chemical compound widely used in scientific experiments, particularly in the fields of bio-pharmacology and biochemistry. It belongs to the group of psoralens, which exhibit phototoxic activity and are employed in research to explore chemical reaction mechanisms and biological effects on cells. This compound is commonly found in traditional medicine ingredients and is used for studies on pharmacological effects and antimicrobial activity. Its unique chemical properties make it a valuable tool for researchers seeking to understand molecular interactions and chemical reactions.

Psoralidin is preferred due to its stable chemical structure under specific conditions and its sensitivity to ultraviolet light. These properties allow it to be used in controlled environments where light exposure can be regulated. Its complex molecular structure also makes it ideal for studying molecular interactions and chemical reactivity. Researchers appreciate its versatility in various experimental setups, as it can be manipulated to study different biological responses. This compound is particularly useful in experiments that require precise control over chemical and biological processes.

In Indonesian laboratories, psoralidin is commonly used in research focused on natural compounds and the development of new drugs. Many research institutions and universities utilize this compound for experiments related to bioactivity and pharmacological effects, especially in the fields of pharmacology and biochemistry. Its presence in traditional medicine formulations also makes it relevant for studies on herbal remedies and their potential therapeutic applications.

TCI brochures (PDF)

Crude Medicine Ingredients for Cancer Research 2025-02-17 · p. 1
Polyphenols 2024-12-05 · p. 2
Phytochemicals 2025-12-17 · p. 9

Related TCI products

Psoralidin is used in bio-pharmacological studies to investigate the pharmacological effects of natural compounds on cellular processes.
It is applied in biochemical research to explore the mechanisms of chemical reactions and the biological effects of phototoxic compounds.
The compound is utilized in antimicrobial research to assess its potential as a natural antimicrobial agent in traditional medicine.
Psoralidin supports molecular interaction studies due to its complex structure, aiding in understanding molecular binding and reactivity.
It is employed in drug development research to evaluate the bioavailability and efficacy of natural compounds in pharmaceutical formulations.

Brand	TCI
CAS number	18642-23-4
Molecular formula	—
Purity	—
Category	Life Science > Biochemicals and Reagents > Crude Medicine Ingredients for Research and Experimental Use
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid, crystalline or powder, depending on the batch
Storage	Store in a cool, dark place away from direct sunlight

Psoralidin should be stored in a cool, dark environment to prevent degradation due to its sensitivity to ultraviolet light. It is recommended to use amber-colored glass containers to minimize light exposure. The compound should be kept in a dry place with controlled temperature to maintain its chemical stability. Proper ventilation is essential when handling this substance to avoid inhalation of vapors. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when working with psoralidin. It is important to follow standard safety protocols to ensure safe handling and prevent any potential hazards in the laboratory setting.

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