galactaric acid
galactosaccharic acid

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  Product(s):
  526-99-8 Mucic acid

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  M0466 Mucic Acid >97.0%(T)
  SDS

Name: (2S,3R,4S,5R)-2,3,4,5-tetrahydroxyhexanedioic acid CAS Number: 526-99-8 3D/inchi Other(deleted CASRN): 1024869-11-1 ECHA EINECS - REACH Pre-Reg: 208-404-0 FDA UNII: E149J5OTIF Nikkaji Web: J6.665F Beilstein Number: 1728117 MDL: MFCD00004239 XlogP3-AA: -2.50 (est) Molecular Weight: 210.13930000 Formula: C6 H10 O8 NMR Predictor: Predict (works with chrome, Edge or firefox) Category:chelating agents   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, 3300 mg/L @ 14C (exp)   Organoleptic Properties: Odor and/or flavor descriptions from others (if found).   Cosmetic Information: CosIng: cosmetic data Cosmetic Uses: chelating agents   Suppliers: BOC Sciences For experimental / research use only. Mucic acid Carbosynth For experimental / research use only. Mucic acid EMD Millipore For experimental / research use only. Mucic Acid sds Givaudan Muciliance® Fruit Odor: characteristic Use: Muciliance® Fruit is a powder of mucic acid obtained from fruit-derived pectins (citrus). Thanks to its potent chelating properties, Muciliance® Fruit is a natural alternative to EDTA that protects the skin from oxidative stress. Santa Cruz Biotechnology For experimental / research use only. Mucic acid ≥97% Sigma-Aldrich: Aldrich For experimental / research use only. Mucic acid 97% sds TCI AMERICA For experimental / research use only. Mucic Acid >97.0%(T) 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: chelating agents Recommendation for galactaric acid usage levels up to:   not for fragrance use.   Recommendation for galactaric 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 Substance Registry Services (TSCA):526-99-8 EPA ACToR:Toxicology Data EPA Substance Registry Services (SRS):Registry Laboratory Chemical Safety Summary :3037582 National Institute of Allergy and Infectious Diseases:Data WGK Germany:2 (2S,3R,4S,5R)-2,3,4,5-tetrahydroxyhexanedioic acid Chemidplus:0000526998 RTECS:LW5180000 for cas# 526-99-8   References:   (2S,3R,4S,5R)-2,3,4,5-tetrahydroxyhexanedioic acid NIST Chemistry WebBook: Search Inchi Canada Domestic Sub. List: 526-99-8 Pubchem (cid): 3037582 Pubchem (sid): 134978406   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 CHEMBL: View Golm Metabolome Database: Search KEGG (GenomeNet): C00879 HMDB (The Human Metabolome Database): HMDB00639 FooDB: FDB001205 Export Tariff Code: 2917.19.2700 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   peach plant Search Trop Picture   Synonyms: D- galactaric acid dextro- galactaric acid meso- galactaric acid   galactosaccharic acid   mucic acid 1,2,3,4- tetrahydroxy-1,4-butanedicarboxylic acid   tetrahydroxyadipic acid (2S,3R,4S,5R)-2,3,4,5- tetrahydroxyhexanedioic acid   Articles:   None found yet. Try the PubMed Search.

Notes: Present in ripe fruits of peach and pear. Formed in grapes and grape must by the action of Botrytis cinerea on galacturonic acid Galactaric acid is the dicarboxylic sugar acid resulting from oxidation glactose with dilute nitric acid. It is a substrate of galactarate O-hydroxycinnamoyltransferase [EC 2.3.1.130]. (KEGG); It forms a crystalline powder which melts at 213 °C. It is insoluble in alcohol, and nearly insoluble in cold water. Due to the symmetry in the molecule, it is optically inactive even though it has chiral carbon atoms (i.e., it is a meso compound). When heated with pyridine to 140 °C, it is converted into allommic acid. When digested with fuming hydrochloric acid for some time it is converted into a 2,5-furandicarboxylic acid (FDCA) while on heating with barium sulfide it is transformed into athiophene carboxylic acid. The ammonium salt yields on dry distillation carbon dioxide, ammonia, pyrrol and other substances. The acid when fused with caustic alkalis yields oxalic acid.