diacetylcurcumin
curcumin 4,4'-diacetate
 
Notes:
None found
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[4-[(1E,6E)-7-(4-acetyloxy-3-methoxyphenyl)-3,5-dioxohepta-1,6-dienyl]-2-methoxyphenyl] acetate (Click)
CAS Number: 19697-86-0Picture of molecule
FDA UNII: 5PUQ5907YX
Nikkaji Web: J744.656J
XlogP3-AA: 3.40 (est)
Molecular Weight: 452.45988000
Formula: C25 H24 O8
NMR Predictor: Predict (works with chrome or firefox)
Category: cosmetic agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
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Google Patents: Search
US Patents: Search
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Pubchem Patents: Search
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Physical Properties:
Food Chemicals Codex Listed: No
Soluble in:
 water, 0.6054 mg/L @ 25 °C (est)
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Organoleptic Properties:
  
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: antioxidants
bleaching agents
skin conditioning
skin protecting agents
uv absorbers
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Suppliers:
 None found
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Safety Information:
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: cosmetic agents
Recommendation for diacetylcurcumin usage levels up to:
 not for fragrance use.
 
Recommendation for diacetylcurcumin flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 6441419
National Institute of Allergy and Infectious Diseases: Data
 [4-[(1E,6E)-7-(4-acetyloxy-3-methoxyphenyl)-3,5-dioxohepta-1,6-dienyl]-2-methoxyphenyl] acetate
Chemidplus: 0019697860
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References:
 [4-[(1E,6E)-7-(4-acetyloxy-3-methoxyphenyl)-3,5-dioxohepta-1,6-dienyl]-2-methoxyphenyl] acetate
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 6441419
Pubchem (sid): 135123258
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Other Information:
(IUPAC): Atomic Weights of the Elements 2009
(IUPAC): Atomic Weights of the Elements 2009 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
CHEMBL: View
HMDB (The Human Metabolome Database): Search
ChemSpider: View
Wikipedia: View
RSC Learn Chemistry: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
 acetic acid, 4-[7-(4-acetoxy-3-methoxy-phenyl)-3,5-dioxo-hepta-1,6-dienyl]-2-methoxy-phenyl ester
1,7-bis(4-(acetyl oxy)-3-methoxyphenyl)-1,6-heptadiene-3,5-dione
[4-[(1E,6E)-7-(4-acetyloxy-3-methoxyphenyl)-3,5-dioxohepta-1,6-dienyl]-2-methoxyphenyl] acetate
 curcumin 4,4'-diacetate
 curcumin bis-acetate
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Articles:
PubMed: Erratum to: Investigating the effect of gallium curcumin and gallium diacetylcurcumin complexes on the structure, function and oxidative stability of the peroxidase enzyme and their anticancer and antibacterial activities.
PubMed: The biological effects of vanadyl curcumin and vanadyl diacetylcurcumin complexes: the effect on structure, function and oxidative stability of the peroxidase enzyme, antibacterial activity and cytotoxic effect.
PubMed: Investigating the effect of gallium curcumin and gallium diacetylcurcumin complexes on the structure, function and oxidative stability of the peroxidase enzyme and their anticancer and antibacterial activities.
PubMed: Evaluation of in vitro antileishmanial activity of curcumin and its derivatives "gallium curcumin, indium curcumin and diacethyle curcumin".
PubMed: Binding analysis for interaction of diacetylcurcumin with β-casein nanoparticles by using fluorescence spectroscopy and molecular docking calculations.
PubMed: An investigation of the molecular interactions of diacetylcurcumin with ribonuclease A.
PubMed: Curcumin derivatives: molecular basis of their anti-cancer activity.
PubMed: Analysis of binding interaction of curcumin and diacetylcurcumin with human and bovine serum albumin using fluorescence and circular dichroism spectroscopy.
PubMed: Interaction of curcumin and diacetylcurcumin with the lipocalin member beta-lactoglobulin.
PubMed: Different curcuminoids inhibit T-lymphocyte proliferation independently of their radical scavenging activities.
PubMed: Investigating the binding of curcumin derivatives to bovine serum albumin.
PubMed: Effects of manganese complexes of curcumin and diacetylcurcumin on kainic acid-induced neurotoxic responses in the rat hippocampus.
PubMed: Prevention of kainic acid-induced changes in nitric oxide level and neuronal cell damage in the rat hippocampus by manganese complexes of curcumin and diacetylcurcumin.
PubMed: Synthesis and characterization of dual function vanadyl, gallium and indium curcumin complexes for medicinal applications.
PubMed: Manganese complexes of curcumin analogues: evaluation of hydroxyl radical scavenging ability, superoxide dismutase activity and stability towards hydrolysis.
PubMed: Evaluation of the nitric oxide radical scavenging activity of manganese complexes of curcumin and its derivative.
PubMed: Manganese complexes of curcumin and its derivatives: evaluation for the radical scavenging ability and neuroprotective activity.
PubMed: Nitric oxide scavenging by curcuminoids.
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