apigeninidin chloride

5,7-dihydroxy-2-(4-hydroxyphenyl)-1-benzopyrylium chloride

CAS: 1151-98-0 C15 H11 Cl O4 MW: 290.70147000

Identification

Nameapigeninidin chloride
IUPAC2-(4-hydroxyphenyl)chromenylium-5,7-diol;chloride
CAS Number1151-98-0
FDA UNIICWI2JJB0W1
Molecular FormulaC15 H11 Cl O4
Molecular Weight290.70147000
MDL NumberMFCD00084721

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Flash Point 32.00 °F. TCC ( 0.00 °C. ) (est)
Soluble in water, 33.63 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for apigeninidin chloride usage levels up tonot for fragrance use.
Recommendation for apigeninidin chloride flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

sorghum

Synonyms

apigeninidin 1- benzopyrylium, 5,7-dihydroxy-2-(4-hydroxyphenyl)-, chloride 5,7- dihydroxy-2-(4-hydroxyphenyl)-1-benzopyrylium chloride 2-(4- hydroxyphenyl)chromenylium-5,7-diol;chloride PubMed: Novel pyrano and vinylphenol adducts of deoxyanthocyanidins in sorghum sourdough. PubMed: Expression level of a flavonoid 3'-hydroxylase gene determines pathogen-induced color variation in sorghum. PubMed: Red card for pathogens: phytoalexins in sorghum and maize. PubMed: The Dermal Layer of Sweet Sorghum (Sorghum bicolor) Stalk, a Byproduct of Biofuel Production and Source of Unique 3-Deoxyanthocyanidins, Has More Antiproliferative and Proapoptotic Activity than the Pith in p53 Variants of HCT116 and Colon Cancer Stem Cells. PubMed: Mutagenesis breeding for increased 3-deoxyanthocyanidin accumulation in leaves of Sorghum bicolor (L.) Moench: a source of natural food pigment. PubMed: Phytochemicals in sweet sorghum ( Dura ) and their antioxidant capabilities against lipid oxidation. PubMed: Antioxidant properties of 3-deoxyanthocyanidins and polyphenolic extracts from Côte d'Ivoire's red and white sorghums assessed by ORAC and in vitro LDL oxidisability tests. PubMed: Host specificity of Sporisorium reilianum is tightly linked to generation of the phytoalexin luteolinidin by Sorghum bicolor. PubMed: New highly stable dimeric 3-deoxyanthocyanidin pigments from sorghum bicolor leaf sheath. PubMed: Uncommonly high levels of 3-deoxyanthocyanidins and antioxidant capacity in the leaf sheaths of dye sorghum. PubMed: Stability of apigeninidin and its methoxylated derivatives in the presence of sulfites. PubMed: C-glycosylanthocyanidins synthesized from C-glycosylflavones. PubMed: Quantitative analysis of anticancer 3-deoxyanthocyanidins in infected sorghum seedlings. PubMed: Collagen and muscle stain obtained from Sorghum bicolor. PubMed: Evaluation of the effect of germination on phenolic compounds and antioxidant activities in sorghum varieties. PubMed: Synergistic effect of deoxyanthocyanins from symbiotic fern Azolla spp. on hrmA gene induction in the cyanobacterium Nostoc punctiforme. PubMed: Antioxidant capacity of a 3-deoxyanthocyanidin from soybean. PubMed: Synthesis of 7-methoxyapigeninidin and its fungicidal activity against Gloeocercospora sorghi. PubMed: Isolation of apigeninidin from leaf sheaths ofSorghum caudatum. PubMed: Effect of apigeninidin on the growth of selected bacteria. PubMed: Effect of apiforol and apigeninidin on growth of selected fungi. PubMed: Phytoalexin synthesis by the sorghum mesocotyl in response to infection by pathogenic and nonpathogenic fungi. PubMed: Structure--activity relationships in the mutagenicity of quinone methides of 7-hydroxyflavylium salts for Salmonella typhimurium. PubMed: Relationships between the development of adventitious roots and the biosynthesis of anthocyanins in first internodes of sorghum. PubMed: Regulatory Mechanisms in Anthocyanin Biosynthesis in First Internodes of Sorghum vulgare: Effect of Presumed Inhibitors of Protein Synthesis.