Petunidin chloride

Base Information

• Chemical Name: Petunidin chloride
• CAS No.: 1429-30-7
• Molecular Formula: C16H13 O7 . Cl
• Molecular Weight: 352.728
• Hs Code.: 2909499000
• European Community (EC) Number: 215-849-4
• NSC Number: 11907
• UNII: WRK4Q8K2D8
• Wikipedia: Petunidin
• Wikidata: Q3137150
• NCI Thesaurus Code: C68449
• Mol file: 1429-30-7.mol

Synonyms:petunidin

Chemical Property of Petunidin chloride

Chemical Property:

• Refractive Index: 1.4790 (estimate)
• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 123.52000
• Density: g/cm³
• LogP: -0.07850
• Storage Temp.: ?20°C
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 2
• Exact Mass: 352.0349804
• Heavy Atom Count: 24
• Complexity: 406

Purity/Quality:

99%, ^*data from raw suppliers

PetunidinChloride ^*data from reagent suppliers

Safty Information:

• Hazard Codes: F,T
• Statements: 11-23/24/25-39/23/24/25
• Safety Statements: 16-36/37-45

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=CC(=CC(=C1O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O.[Cl-]
• Description: Petunidin is an O-methylated anthocyanidin derived from delphinidin that imparts blue-red pigments to flowers, fruits, and red wine. It has been shown to bind with and suppress the activity of focal adhesion kinase and to inhibit platelet-derived growth factor-induced aortic smooth muscle cell migration, which may confer a protective effect against atherosclerosis. Extracts from E. jambolana fruit, which is rich in anthocyanins including petunidin, have been used to suppress the proliferation of an HCT116 colon cancer cell line, as well as colon cancer stem cells.
• Uses: Petunidin chloride is the chloride salt of Petunidin, an anthocyanin pigment that contributes to the bluish colour in flowers such as the Petunia hybrida and in fruits such as blueberries.

Technology Process of Petunidin chloride

There total 2 articles about Petunidin chloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ petunidin (1429-30-7)

Guidance literature:

With sodium hydroxide; unter Wasserstoff und Erwaermen der mit wss. Salzsaeure angesaeuerten Reaktionsloesung;

DOI:10.1021/ac60046a027

Reference yield:

→ petunidin (1429-30-7)

Guidance literature:

With hydrogenchloride;

Reference yield:

petunidin (1429-30-7) → 3,5-dihydroxyphenol (108-73-6)

Guidance literature:

at 140 ℃;

Downstream raw materials:

3,5-dihydroxyphenol

petunidin 3-O-glucoside chloride