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

oxalic acid dihydrate
ethanedioic acid, hydrate (1:2)

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CAS Number: 6153-56-6Picture of molecule3D/inchi
FDA UNII: 0K2L2IJ59O
Beilstein Number:3679436
MDL:MFCD00149102
Molecular Weight:126.06502000
Formula:C2 H6 O6
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:pharmaceuticals / chemical synthisis
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
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Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Appearance:white to pale yellow powder (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 101.50 °C. @ 760.00 mm Hg
Flash Point: 32.00 °F. TCC ( 0.00 °C. ) (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.
Oxalic acid dihydrate 95%
Capot Chemical
Oxalic Acid Dihydrate
Charkit Chemical
OXALIC ACID
ECSA Chemicals
OXALIC ACID DIHYDRATE 99% FEINCRYST.
ECSA TRADE THE MOST UPDATED FINANCIAL PUBLICATION ON THE WORLD OF CHEMISTRY
EMD Millipore
For experimental / research use only.
Oxalic Acid Dihydrate
sds
Glentham Life Sciences
Oxalic acid dihydrate
Penta International
OXALIC ACID DIHYDRATE
Santa Cruz Biotechnology
For experimental / research use only.
Oxalic Acid Dihydrate
Sigma-Aldrich
For experimental / research use only.
Oxalic acid dihydrate ACS reagent, ≥99%
Universal Preserv-A-Chem Inc.
OXALIC ACID DIHYDRATE TECH
Odor: characteristic
Use: It is used in the pharmaceutical and idustrial fields. Used as a precipitating and separating function for rare-earth metal. In pharmaceuticals it is used in Tetracyline, Oxtetracycline, Phenobarbital,and Borneol,etc. It is also used as a reducing agent for dyeing and printing industry,as bleaching agent for textile,substitute for acetic acid,as coloring mordant for fast pigment dyestuff.
 
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:
pharmaceuticals / chemical synthisis
Recommendation for oxalic acid dihydrate usage levels up to:
 not for fragrance use.
 
Recommendation for oxalic acid dihydrate flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
NIOSH International Chemical Safety Cards:search
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :61373
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:1
oxalic acid;dihydrate
Chemidplus:0006153566
RTECS:6153-56-6
 
References:
 oxalic acid;dihydrate
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):61373
Pubchem (sid):135018460
 
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
Export Tariff Code:2917.11.0000
ChemSpider:View
Wikipedia:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 not found in nature
 
Synonyms:
 ethandionic acid
 ethanedioic acid dihydrate
 ethanedioic acid, dihydrate
 ethanedioic acid, hydrate (1:2)
 oxalic acid ACS
 oxalic acid ultra pure grade
 oxalic acid, dihydrate
 oxalic acid;dihydrate
 

Articles:

PubMed:Deuterium MAS NMR studies of dynamics on multiple timescales: histidine and oxalic acid.
PubMed:Cocrystal dissociation in the presence of water: a general approach for identifying stable cocrystal forms.
PubMed:Statistical analysis of multipole-model-derived structural parameters and charge-density properties from high-resolution X-ray diffraction experiments.
PubMed:Synthesis and spectroscopic characterization of magnesium oxalate nano-crystals.
PubMed:Synthesis of a new bis(indolyl)methane that inhibits growth and induces apoptosis in human prostate cancer cells.
PubMed:Proton-conducting supramolecular metallogels from the lowest molecular weight assembler ligand: a quote for simplicity.
PubMed:Effect of waters of crystallization on terahertz spectra: anhydrous oxalic acid and its dihydrate.
PubMed:Hydrogen migration in oxalic acid di-hydrate at high pressure?
PubMed:A practical and efficient synthesis of bis(indolyl)methanes in water, and synthesis of di-, tri-, and tetra(bis-indolyl)methanes under thermal conditions catalyzed by oxalic acid dihydrate.
PubMed:The prior-derived F constraints in the maximum-entropy method.
PubMed:On functions and quantities derived from the experimental electron density.
PubMed:17O quadrupole coupling and chemical shielding tensors in an H-bonded carboxyl group: alpha-oxalic acid.
PubMed:The generalized F constraint in the maximum-entropy method--a study on simulated data.
PubMed:Wavefunctions derived from experiment. III. Topological analysis of crystal fragments.
PubMed:How precise are measurements of unit-cell dimensions from single crystals?
PubMed:Wavefunctions derived from experiment. II. A wavefunction for oxalic acid dihydrate.
PubMed:Particle size distributions from multiparticulate dissolution.
PubMed:17O NMR and crystalline hydrates.
PubMed:In vitro degradation of oxalic acid by human feces.
PubMed:Formation of reduced carbonaceous matter in basalts and xenoliths: reaction of C-O-H gases on olivine crack surfaces.
PubMed:Carbon-isotopic analysis of dissolved acetate.
PubMed:Preparation of 7-hydroxy-2-oxoindolin-3-ylacetic acid and its [13C2], [5-n-3H], and [5-n-3H]-7-O-glucosyl analogues for use in the study of indol-3-ylacetic acid catabolism.
PubMed:Evaluation of growth rate constants of oxalic acid dihydrate at constant supersaturation.
PubMed:Crystallization kinetics of oxalic acid dihydrate: nonisothermal desupersaturation of solutions.
PubMed:Expected particle size distributions of crystals produced from nonisothermal recrystallization.
PubMed:Dissolution rate equations in column-confined dissolution.
PubMed:Dissolution patterns of polydisperse powders: oxalic acid dihydrate.
PubMed:Electron Population Parameters from Least-Squares Refinement of X-ray Diffraction Data.
PubMed:Growth of Oxalic Acid Single Crystals from Solution: Solvent Effects on Crystal Habit.
 
Notes:
None found
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