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(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol (Click)
CAS Number: 9005-84-9Picture of molecule
ECHA EINECS - REACH Pre-Reg: 232-686-4
Nikkaji Web: J247.675D
MDL: MFCD00082026
Molecular Weight: 342.29854000
Formula: C12 H22 O11
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: absorbents, bulking agents
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 667.90 °C. @ 760.00 mm Hg (est)
Flash Point: 676.00 °F. TCC ( 357.80 °C. ) (est)
logP (o/w): -3.410 (est)
Soluble in:
 water, 1e+006 mg/L @ 25 °C (est)
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Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: absorbents
bulking agents
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For experimental / research use only.
Starch, soluble ACS reagent
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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
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: absorbents, bulking agents
Recommendation for amylodextrin usage levels up to:
 not for fragrance use.
Recommendation for amylodextrin flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
Cancer Citations: Search
EPA Substance Registry Services (TSCA): 9005-84-9
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 439341
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 1
Chemidplus: 0009005849
RTECS: GM5090000 for cas# 9005-84-9
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NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 9005-84-9
Pubchem (cid): 439341
Pubchem (sid): 135231875
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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
KEGG (GenomeNet): C00897
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 3505.10.0090
ChemSpider: View
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Potential Blenders and core components note
None Found
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Potential Uses:
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Occurrence (nature, food, other): note
 not found in nature
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 starch soluble
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PubMed: Plasticisation of amylodextrin by moisture: consequences for drug release from tablets.
PubMed: 13C-N.M.R. study of the conformation of helical complexes of amylodextrin and of amylose in solution.
PubMed: Preparation, characterization, and pharmaceutical application of linear dextrins. II. Complexation and dispersion of drugs with amylodextrin by freeze-drying and kneading.
PubMed: Plasticisation of amylodextrin by moisture. Consequences for compaction behaviour and tablet properties.
PubMed: Controlled release of theophylline monohydrate from amylodextrin tablets: in vitro observations.
PubMed: Preparation, characterization, and pharmaceutical application of linear dextrins. III. Drug release from fatty suppository bases containing amylodextrin.
PubMed: Preparation, characterization and pharmaceutical application of linear dextrins. I. Preparation and characterization of amylodextrin, metastable amylodextrins, and metastable amylose.
PubMed: Controlled release of paracetamol from amylodextrin tablets: in vitro and in vivo results.
PubMed: The malQ gene is essential for starch metabolism in Streptococcus mutans.
PubMed: Complexation between Amylodextrin Oligomers and Selected Pharmaceuticals Measured through Capillary Electrophoresis.
PubMed: A flow-calorimetric study of the binding of iodine to amylodextrin fractions.
PubMed: An improved assay method for amylase activity using an amylodextrin fraction as substrate.
PubMed: Iodine binding to amylodextrin fractions studied by difference spectrophotometry and potentiometry.
PubMed: Use of isoelectric focusing to characterize the bonds established during coupling of CNBr-activated amylodextrin to subtilisin type novo.
PubMed: The effect of inorganic ions on the crystallization of amylodextrin.
PubMed: The mechanism of degradation of starch by amylases: The action of malt amylase on alpha-amylodextrin.
PubMed: Preparation of linear maltodextrins using a hyperthermophilic amylopullulanase with cyclodextrin- and starch-hydrolysing activities.
PubMed: Doubling Power Output of Starch Biobattery Treated by the Most Thermostable Isoamylase from an Archaeon Sulfolobus tokodaii.
PubMed: Effects of lipids on enzymatic hydrolysis and physical properties of starch.
PubMed: TEMPO electromediated oxidation of some polysaccharides including regenerated cellulose fiber.
PubMed: Interference prevention in size-exclusion chromatographic analysis of debranched starch glucans by aqueous system.
PubMed: Circular dichroism studies on glycogen phosphorylase from rabbit muscle. Interaction with the allosteric activator adenosine 5'-monophosphate.
PubMed: The influence of chain size and molecular weight on the kinetic constants for the span glucose to polysaccharide for rabbit muscle glycogen synthase.
PubMed: Structure studies of amylose-V complexes and retrograded amylose by action of alpha amylases, and a new method for preparing amylodextrins.
PubMed: New, simple maltogenic assay for mechanized determination of alpha-amylase activity in serum and urine.
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