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glucosyringic acid

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CAS Number: 33228-65-8Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web:J18.842E
XlogP3:-1.00 (est)
Molecular Weight:360.31640000
Formula:C15 H20 O10
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, 5.52e+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.
Glucosyringic acid >95%
Odor: characteristic
Use: Glucosyringic acid is a natural plant phenol found in herbs of Linaria vulgaris Mill.
 
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 glucosyringic acid usage levels up to:
 not for fragrance use.
 
Recommendation for glucosyringic acid 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 :10383888
National Institute of Allergy and Infectious Diseases:Data
3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoic acid
Chemidplus:0033228658
 
References:
 3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoic acid
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):10383888
Pubchem (cas):33228-65-8
 
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:FDB012010
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 phleum subulatum
Search Trop Picture
 quillaja saponaria
Search Trop Picture
 
Synonyms:
 benzoic acid, 4-(beta-D-glucopyranosyloxy)-3,5-dimethoxy-
3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoic acid
 

Articles:

PubMed:Phenolic constituents in commercial aqueous Quillaja (Quillaja saponaria Molina) wood extracts.
PubMed:[Chemical constituents of Eucommia ulmoides].
PubMed:Effect of sprout extract from Tuscan black cabbage on xenobiotic-metabolizing and antioxidant enzymes in rat liver.
PubMed:[Phenolic acid derivatives from Alchornea trewioides].
PubMed:[Phenolic acid derivatives from Bauhinia glauca subsp. pernervosa].
PubMed:Phenolic compounds from Eurycorymbus cavaleriei.
PubMed:Two new compounds from the dried tender stems of Cinnamomum cassia.
PubMed:New isoflavone glycosides from Iris spuria L. (Calizona) cultivated in Egypt.
PubMed:Antioxidant and 15-lipoxygenase inhibitory activity of rotenoids, isoflavones and phenolic glycosides from Sarcolobus globosus.
PubMed:[Studies on chemical constituents from roots of Polygala tricornis].
PubMed:Diterpenoid and phenolic glycosides from the roots of Rhododendron molle.
PubMed:[Chemical constituents of Sageretia theezans Brongn].
 
Notes:
None found
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