amylodextrin
 
Notes:
None found
  • ECSA Chemicals
    • ECSA Chemicals
      Human Chemistry
      ECSA Chemicals has been active since 1913 in the trading and international commerce of raw materials. With an organisation divided into industrial segments managed by specialists, it has become one of the largest distributors worldwide.
      ECSA Chemicals is the largest Swiss-owned company in terms of warehouses for the distribution of chemical products. We have been distributing chemical products for over 100 years and we have a special interest in protecting the environment and in the safety of our facilities and collaborators.
      Established in 1913 as a small grocery store, in its over 100 years of activity ECSA Chemicals has become one of the most important Swiss-owned distributors of chemical products. The company, which is active in international distribution and trading, is organised into industrial segments that are managed by teams of specialists and experts. They guarantee professional and customised consultancy and services. With our experience, we can rapidly and safely connect you with the best suppliers on the market, providing you with a complete search, consulting and assistance service. The focus of our approach and operations is you, our customers. We strive every day to find the best products that satisfy your needs as quickly as possible. Your satisfaction is our greatest success. WHY CHOOSE ECSA? EXPERIENCE We have been working for 100 years. QUALITY We have obtained many certifications (ISO, SQAS, GDP, Responsible Care, Bio-Inspecta, RSPO, etc.). We guarantee full compliance with the current laws and continuous training for our staff. SAFETY We constantly carry out risk analyses for each infrastructure, defining safety levels and implementing corrective measures promptly wherever they are needed. WIDESPREAD DISTRIBUTION We have warehouses in strategic locations to supply goods to Switzerland and to the rest of the world. STORAGE CAPACITY The 3 ECSA-owned warehouses guarantee considerable storage area and capacity in each warehouse, with full availability of products (base chemicals and speciality chemicals). SPEED Presence all over the country, staff dedicated to sourcing raw materials and considerable storage capacity guarantee that goods are rapidly obtained and supplied. CONSULTANCY Our specialists - in-depth knowledge of the market and products allows us to provide full consulting services, from the purchase to the supply of raw materials.
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      Products List: View
      Product(s):
      RE-417585 STARCH SOLUBLE RPE-ACS-FOR ANALYSIS-REAG. PH
      RE-477302 STARCH PASTE SOLUTION 1% IN WATER RPE-FOR AN
       
  • Glentham Life Sciences
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CAS Number: 9005-84-9Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 232-686-4
FDA UNII: 15SUG9AD26
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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Suppliers:
ECSA Chemicals
STARCH PASTE SOLUTION 1% IN WATER RPE-FOR AN
ECSA TRADE THE MOST UPDATED FINANCIAL PUBLICATION ON THE WORLD OF CHEMISTRY
ECSA Chemicals
STARCH SOLUBLE RPE-ACS-FOR ANALYSIS-REAG. PH
Glentham Life Sciences
Starch, soluble, ACS grade
Sigma-Aldrich
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
 
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: 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
AIDS Citations: Search
Cancer Citations: Search
Toxicology 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
 (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
Chemidplus: 0009005849
RTECS: GM5090000 for cas# 9005-84-9
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References:
 (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
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 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): 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:
 absorbents 
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
 starch soluble
(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
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Articles:
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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