EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

citroside A

Supplier Sponsors

CAS Number: 120330-44-1Picture of molecule3D/inchi
FDA UNII: Search
XlogP3-AA:-1.60 (est)
Molecular Weight:386.44170000
Formula:C19 H30 O8
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:natural substances and extractives
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Soluble in:
 water, 1.014e+004 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
Citroside A 96%
 
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
 
Safety in Use Information:
Category:
natural substances and extractives
Recommendation for citroside A usage levels up to:
 not for fragrance use.
 
Recommendation for citroside A flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :14312560
National Institute of Allergy and Infectious Diseases:Data
4-[4-hydroxy-2,2,6-trimethyl-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexylidene]but-3-en-2-one
Chemidplus:0120330441
 
References:
 4-[4-hydroxy-2,2,6-trimethyl-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexylidene]but-3-en-2-one
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):14312560
Pubchem (cas):120330-44-1
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
HMDB (The Human Metabolome Database):Search
FooDB:FDB002216
VCF-Online:VCF Volatile Compounds in Food
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 potentilla multifida
Search Trop Picture
 
Synonyms:
4-[4-hydroxy-2,2,6-trimethyl-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexylidene]but-3-en-2-one
 

Articles:

PubMed:Skin depigmenting action of silkworm (Bombyx mori L.) droppings in zebrafish.
PubMed:[Study on active constituents against Alzheimer's disease from Valeriana amurensis].
PubMed:A new megastigmane glycoside from the aerial parts of Cirsium setosum.
PubMed:Crotonionosides A-G: megastigmane glycosides from leaves of Croton cascarilloides Räuschel.
PubMed:Schefflerins A-G, new triterpene glucosides from the leaves of Schefflera arboricola.
PubMed:Elaeocarpionoside, a megastigmane glucoside from the leaves of Elaeocarpus japonicus Sieb. et Zucc.
PubMed:Two new megastigmane glycosides, physanosides A and B, from Physalis alkekengi L. var. franchetii, and their effect on NO release in macrophages.
PubMed:Cuneatoside, a new megastigmane diglycoside from Erythroxylum cuneatum Blume.
PubMed:[The megastigman glycosides from herb of Potentilla multifida].
PubMed:Acetophenone diglycosides from Erythroxylum cambodianum.
PubMed:Norsesquiterpenoid and sesquiterpenoid glycosides from Evodia austrosinensis.
PubMed:Lasianthionosides A-C, megastigmane glucosides from leaves of Lasianthus fordii.
PubMed:An iridoid glucoside dimer and a non-glycosidic iridoid from the leaves of Lasianthus wallichii.
PubMed:Inhibitory effects of glycosides from the leaves of Melaleuca quinquenervia on vascular contraction of rats.
PubMed:Phlomisflavosides A and B, new flavonol bisglycosides from Phlomis spinidens.
PubMed:C(13)-Norisoprenoid glucoconjugates from lulo (Solanum quitoense L.) leaves.
 
Notes:
None found
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