SMB01083

4,5-Di-O-caffeoylquinic acid methyl ester

≥90% (LC/MS-ELSD)

• Synonyme(s) : Methyl (1R,3R,4S,5R)-3,4-bis[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy]-1,5-dihydroxycyclohexane-1-carboxylate
• Formule empirique (notation de Hill): C₂₆H₂₆O₁₂
• Numéro CAS: 188742-80-5
• Poids moléculaire : 530.48
• Code UNSPSC : 12352205
• Nomenclature NACRES : NA.25

Propriétés

• Source biologique: plant
• Pureté: ≥90% (LC/MS-ELSD)
• Forme: solid
• Poids mol.: 530.48
• Application(s): metabolomics; vitamins, nutraceuticals, and natural products
• Température de stockage: −20°C

Description

Description générale

4,5-Di-O-caffeoylquinic acid methyl ester, a phenylpropanoid, belongs to group of compounds known as cyclic alcohols and derivatives. It is a natural product commonly available from Erigeron breviscapus, Spuriopimpinella brachycarpa, Ipomoea batatas L., and Spuriopimpinella calycina plants. Studies have demonstrated that this metabolite, derived from plant sources, possesses various biological activities, including antioxidant and antiviral properties.

Application

It is a natural product derived from plant source that finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research.

Actions biochimiques/physiologiques

4,5-Di-O-caffeoylquinic acid methyl ester demonstrates strong antioxidant activity with significant free radical-scavenging abilities against DPPH. Additionally, it displays in vitro antiviral activity against the respiratory syncytial virus.

Caractéristiques et avantages

• High quality compound suitable for multiple research applications
• Compatible with HPLC and mass spectrometry techniques

Autres remarques

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Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable