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

neohesperidose
2-O-a-L-rhamnosyl-D-glucose

Supplier Sponsors

Name:(2S,3R,4R,5R,6S)-2-methyl-6-[(2R,3R,4S,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol
CAS Number: 17074-02-1Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:241-133-6
FDA UNII: Search
Nikkaji Web:J3.288.339G
MDL:MFCD00064919
XlogP3-AA:-3.70 (est)
Molecular Weight:326.29934000
Formula:C12 H22 O10
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:information only not used for fragrances or flavors
 
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
Boiling Point: 633.90 °C. @ 760.00 mm Hg (est)
Flash Point: 639.00 °F. TCC ( 337.20 °C. ) (est)
logP (o/w): -0.440 (est)
Soluble in:
 water, 1e+006 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.
Neohesperidose
Carbosynth
For experimental / research use only.
neoHesperidose
Glentham Life Sciences
neoHesperidose
Santa Cruz Biotechnology
For experimental / research use only.
neoHesperidose
Sigma-Aldrich: Sigma
For experimental / research use only.
neoHesperidose ≥90%
sds
 
Safety Information:
Preferred SDS: View
 
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:
information only not used for fragrances or flavors
Recommendation for neohesperidose usage levels up to:
 not for fragrance use.
 
Recommendation for neohesperidose 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 :441426
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
(2S,3R,4R,5R,6S)-2-methyl-6-[(2R,3R,4S,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol
Chemidplus:0017074021
 
References:
 (2S,3R,4R,5R,6S)-2-methyl-6-[(2R,3R,4S,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):441426
Pubchem (sid):36885262
 
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
CHEBI:View
KEGG (GenomeNet):C08244
HMDB (The Human Metabolome Database):HMDB29523
FooDB:FDB000660
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 found in food but not in nature
 
Synonyms:
β-D-glucopyranose, 2-O-(6-deoxy-a-L-mannopyranosyl)-
(2S,3R,4R,5R,6S)-2-methyl-6-[(2R,3R,4S,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol
2-O-a-L-rhamnosyl-D-glucose
 

Articles:

PubMed:Targeting structural motifs of flavonoid diglycosides using collision-induced dissociation experiments on flavonoid/Pb2+ complexes.
PubMed:Screening and identification of disaccharides with insulin mimetic activity against L6 cells.
PubMed:Characteristic fragmentation patterns of trimethylsilyl and trimethylsilyl-oxime derivatives of plant disaccharides as obtained by gas chromatography coupled to ion-trap mass spectrometry.
PubMed:Study of kaempferol glycoside as an insulin mimic reveals glycon to be the key active structure.
PubMed:Silver complexation and tandem mass spectrometry for differentiation of isomeric flavonoid diglycosides.
PubMed:Threshold dissociation and molecular modeling of transition metal complexes of flavonoids.
PubMed:Characterization of flavonoids by aluminum complexation and collisionally activated dissociation.
PubMed:Gas-phase hydrogen/deuterium exchange and conformations of deprotonated flavonoids and gas-phase acidities of flavonoids.
PubMed:Influence of a sugar moiety (rhamnosylglucoside) at 3-O position on the reactivity of quercetin with whey proteins.
PubMed:Structure characterization of flavonoid O-diglycosides by positive and negative nano-electrospray ionization ion trap mass spectrometry.
PubMed:Structural characterization of flavonoid glycosides by collisionally activated dissociation of metal complexes.
PubMed:Preparation and taste of certain glycosides of flavanones and of dihydrochalcones.
PubMed:The antiatherogenic effects of components isolated from pollen typhae.
 
Notes:
Occurs in plants as disaccharide component of HBH63-H and other glycosides
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