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TCI

CAS 4261-42-1

Isoorientin TCI I1087

Isoorientin TCI I1087

Chemical Identity

CAS No.
4261-42-1
Formula
C21H20O11
Molecular weight
448.4 g/mol
Purity
>98.0%(HPLC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one
SMILES
C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)O)O
InChIKey
ODBRNZZJSYPIDI-VJXVFPJBSA-N
PubChem
CID 114776
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Isoorientin is a chemical compound classified within the flavonoid family, known for its complex molecular structure and widespread use in biochemical research. This compound is commonly found in medicinal plants such as *Vitex negundo* and is valued for its biological activities, including antioxidant and anti-inflammatory properties. In the laboratory, Isoorientin plays a crucial role in studying the mechanisms of biological activity, drug development, and the analysis of phenolic compounds. Its stability and ease of analysis make it a reliable choice for various chemical and biological experiments.

One of the key reasons Isoorientin is preferred is its unique chemical properties. It exhibits solubility in organic solvents like ethyl acetate and ethanol, which facilitates its use in analytical techniques. Additionally, its complex molecular structure enables it to interact with proteins and enzymes, making it highly relevant for molecular interaction studies. The availability of Isoorientin in pure form and adjustable concentrations allows for its application in a wide range of analytical methods, including spectroscopy and chromatography.

In Indonesian laboratories, Isoorientin is frequently used in pharmacology, organic chemistry, and biotechnology research. Its role in studying natural products and their therapeutic potential is particularly significant. Researchers rely on Isoorientin to explore its biological effects and to develop new compounds with potential medicinal applications. Its versatility and reliability make it an essential component in many scientific investigations.

  • Drug development studies benefit from Isoorientin’s antioxidant and anti-inflammatory properties, aiding in the discovery of new therapeutic agents.
  • Biochemical research utilizes Isoorientin to investigate molecular interactions with proteins and enzymes, enhancing understanding of biological mechanisms.
  • Phenolic compound analysis leverages Isoorientin’s solubility in organic solvents, enabling accurate identification and quantification in complex mixtures.
  • Pharmacological studies use Isoorientin to explore its potential therapeutic effects, supporting research into natural product-based medicines.
  • Chromatographic and spectroscopic analyses rely on Isoorientin’s stability and purity, ensuring reliable results in analytical procedures.

Brand TCI
CAS number 4261-42-1
Molecular formula —
Purity —
Category Chemistry > Chemical Biology > Glycoscience
Pack sizes Available in various quantities as per standard laboratory requirements
Physical form Solid
Storage Store in a cool, dry place away from light

Isoorientin should be stored in a cool, dry place away from direct light to maintain its stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and air, which could affect its chemical integrity. Due to its solubility in organic solvents, it is important to handle Isoorientin with care to avoid contamination. In laboratory settings, proper personal protective equipment such as gloves and safety goggles should be worn when handling this compound. Regular monitoring of storage conditions ensures the compound remains suitable for use in analytical and research applications. Always follow standard laboratory safety protocols to ensure safe handling and storage.

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