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Glyoxylic acid monohydrate

CAS 563-96-2C2H2O3MW 74.04

Glyoxylic acid monohydrate (CAS 563-96-2) — formula C2H2O3, molecular weight 74.04; category organic chemicals.

Product Overview

CAS Number563-96-2
Molecular FormulaC2H2O3
Molecular Weight74.04
Melting Point98
LogPlog Kow= -0.07
ApplicationsUses: Found in unripe fruit, young green leaves, and very young sugar beets, [Merck Index] Used to make flavorings, perfumes, cosmetics, pharmaceuticals, dyes, plastics, agricultural chemicals, and vanillin, Also used as a cleaning agent for a variety of industrial applications, [HSDB], INTERMEDIATE FOR FLAVORINGS, PERFUMES, PHARMACEUTICALS, DYES, PLASTICS, AGRICULTURAL CHEMICALS., Cleaning agent for a variety of industrial applications, as a speciality chemical and biodegradable copolymer feedstock., Ingredient in cosmetics, CHEM INT FOR ITS ESTERS-EG, METHYL ESTER (PESTICIDE INT), CHEM INT FOR VANILLIN, Use Classification: Cosmetics -> Buffering, Industry Uses: Other, Intermediate, Corrosion inhibitor, Not Known or Reasonably Ascertainable, Consumer Uses: Not Known or Reasonably Ascertainable, Household Products: Information on 3 consumer products that contain Glyoxylic Acid in the following categories is provided:, • Personal Care, Methods of Manufacturing: Prepd by heating dibromoacetic acid with some water, by electrolytic reduction of oxalic acid, by action of Aspergillus niger on calcium acetate, malonic or citric acid., Formulations, Preparations: SUPPLIED AS A 50% SOLN ... ., U.S. Production: 2023: 1, 000, 000 - <5, 000 lb, 2022: 5, 000 - <10, 2021: 10, 000 - <50, 2020: 5, (1977) NO EVIDENCE OF COMMERCIAL PRODN IN U.S., (1981) NO EVIDENCE OF COMMERCIAL PRODN IN U.S., General Manufacturing Information: Not Known or Reasonably Ascertainable, All Other Basic Organic Chemical Manufacturing, Oil and Gas Drilling, Extraction, and Support activities, Acetic acid, 2-oxo-: ACTIVE, PATIENTS SUFFERING FROM PRIMARY HYPEROXALURIA SHOW ELEVATED PLASMA CONCN OF OXALIC ACID & GLYOXYLIC ACID. IN VITRO ADSORPTION OF THESE CMPD INTO VARIOUS SUBSTANCES WAS INVESTIGATED. HYDROUS ZIRCONIUM OXIDE WAS MOST EFFECTIVE SORBENT STUDIED FOR REMOVAL OF OXALIC ACID & GLYOXYLIC ACID. IN BATCH EXPT, ZIRCONIUM OXIDE WAS CAPABLE OF BINDING 5.5 UMOL OXALIC ACID & 8 UMOL OF GLYOXYLIC ACID, G SORBENT USING 0.5 G SORBENT, L & IONIC COMPOSITION RESEMBLING THAT OF PLASMA. RECIRCULATION OF 2 L OF THE SAME SOLN THROUGH 12 G OF MIXT OF HYDROUS ZIRCONIUM OXIDE & ALUMINA FOR 6 HR AT FLOW RATE OF 12 ML, MIN, RESULTED IN FINAL CONCN OF 70 UMOL, L OF OXALIC ACID & 50 UMOL, L OF GLYOXYLIC ACID.
CategoryOrganic Chemicals

Applications

Documented applications: Uses: Found in unripe fruit, young green leaves, and very young sugar beets, [Merck Index] Used to make flavorings, perfumes, cosmetics, pharmaceuticals, dyes, plastics, agricultural chemicals, and vanillin, Also used as a cleaning agent for a variety of industrial applications, [HSDB], INTERMEDIATE FOR FLAVORINGS, PERFUMES, PHARMACEUTICALS, DYES, PLASTICS, AGRICULTURAL CHEMICALS., Cleaning agent for a variety of industrial applications, as a speciality chemical and biodegradable copolymer feedstock., Ingredient in cosmetics, CHEM INT FOR ITS ESTERS-EG, METHYL ESTER (PESTICIDE INT), CHEM INT FOR VANILLIN, Use Classification: Cosmetics -> Buffering, Industry Uses: Other, Intermediate, Corrosion inhibitor, Not Known or Reasonably Ascertainable, Consumer Uses: Not Known or Reasonably Ascertainable, Household Products: Information on 3 consumer products that contain Glyoxylic Acid in the following categories is provided:, • Personal Care, Methods of Manufacturing: Prepd by heating dibromoacetic acid with some water, by electrolytic reduction of oxalic acid, by action of Aspergillus niger on calcium acetate, malonic or citric acid., Formulations, Preparations: SUPPLIED AS A 50% SOLN ... ., U.S. Production: 2023: 1, 000, 000 - <5, 000 lb, 2022: 5, 000 - <10, 2021: 10, 000 - <50, 2020: 5, (1977) NO EVIDENCE OF COMMERCIAL PRODN IN U.S., (1981) NO EVIDENCE OF COMMERCIAL PRODN IN U.S., General Manufacturing Information: Not Known or Reasonably Ascertainable, All Other Basic Organic Chemical Manufacturing, Oil and Gas Drilling, Extraction, and Support activities, Acetic acid, 2-oxo-: ACTIVE, PATIENTS SUFFERING FROM PRIMARY HYPEROXALURIA SHOW ELEVATED PLASMA CONCN OF OXALIC ACID & GLYOXYLIC ACID. IN VITRO ADSORPTION OF THESE CMPD INTO VARIOUS SUBSTANCES WAS INVESTIGATED. HYDROUS ZIRCONIUM OXIDE WAS MOST EFFECTIVE SORBENT STUDIED FOR REMOVAL OF OXALIC ACID & GLYOXYLIC ACID. IN BATCH EXPT, ZIRCONIUM OXIDE WAS CAPABLE OF BINDING 5.5 UMOL OXALIC ACID & 8 UMOL OF GLYOXYLIC ACID, G SORBENT USING 0.5 G SORBENT, L & IONIC COMPOSITION RESEMBLING THAT OF PLASMA. RECIRCULATION OF 2 L OF THE SAME SOLN THROUGH 12 G OF MIXT OF HYDROUS ZIRCONIUM OXIDE & ALUMINA FOR 6 HR AT FLOW RATE OF 12 ML, MIN, RESULTED IN FINAL CONCN OF 70 UMOL, L OF OXALIC ACID & 50 UMOL, L OF GLYOXYLIC ACID..

Technical Profile

What this product is

Glyoxylic acid monohydrate is a carbon-based organic compound with CAS registry number 563-96-2 and molecular formula C2H2O3 (molecular weight 74.04), belonging to the organic chemicals segment of chemical raw materials.

Identification

CAS number: 563-96-2

Its molecular formula C2H2O3 comprises 2 C, 2 H, 3 O atoms.

Also known as: Glyoxylic acid monohydrate · 乙醛酸一水合物

Category: organic chemicals

Frequently Asked Questions

What is the CAS number of Glyoxylic acid monohydrate?

The CAS registry number of Glyoxylic acid monohydrate is 563-96-2.

What is the molecular formula and molecular weight of Glyoxylic acid monohydrate?

Molecular formula C2H2O3, molecular weight 74.04.

What other names is Glyoxylic acid monohydrate known by?

It is also registered under: Glyoxylic acid monohydrate, 乙醛酸一水合物.

What are the documented applications of Glyoxylic acid monohydrate?

Recorded applications: Uses: Found in unripe fruit, young green leaves, and very young sugar beets, [Merck Index] Used to make flavorings, perfumes, cosmetics, pharmaceuticals, dyes, plastics, agricultural chemicals, and vanillin, Also used as a cleaning agent for a variety of industrial applications, [HSDB], INTERMEDIATE FOR FLAVORINGS, PERFUMES, PHARMACEUTICALS, DYES, PLASTICS, AGRICULTURAL CHEMICALS., Cleaning agent for a variety of industrial applications, as a speciality chemical and biodegradable copolymer feedstock., Ingredient in cosmetics, CHEM INT FOR ITS ESTERS-EG, METHYL ESTER (PESTICIDE INT), CHEM INT FOR VANILLIN, Use Classification: Cosmetics -> Buffering, Industry Uses: Other, Intermediate, Corrosion inhibitor, Not Known or Reasonably Ascertainable, Consumer Uses: Not Known or Reasonably Ascertainable, Household Products: Information on 3 consumer products that contain Glyoxylic Acid in the following categories is provided:, • Personal Care, Methods of Manufacturing: Prepd by heating dibromoacetic acid with some water, by electrolytic reduction of oxalic acid, by action of Aspergillus niger on calcium acetate, malonic or citric acid., Formulations, Preparations: SUPPLIED AS A 50% SOLN ... ., U.S. Production: 2023: 1, 000, 000 - <5, 000 lb, 2022: 5, 000 - <10, 2021: 10, 000 - <50, 2020: 5, (1977) NO EVIDENCE OF COMMERCIAL PRODN IN U.S., (1981) NO EVIDENCE OF COMMERCIAL PRODN IN U.S., General Manufacturing Information: Not Known or Reasonably Ascertainable, All Other Basic Organic Chemical Manufacturing, Oil and Gas Drilling, Extraction, and Support activities, Acetic acid, 2-oxo-: ACTIVE, PATIENTS SUFFERING FROM PRIMARY HYPEROXALURIA SHOW ELEVATED PLASMA CONCN OF OXALIC ACID & GLYOXYLIC ACID. IN VITRO ADSORPTION OF THESE CMPD INTO VARIOUS SUBSTANCES WAS INVESTIGATED. HYDROUS ZIRCONIUM OXIDE WAS MOST EFFECTIVE SORBENT STUDIED FOR REMOVAL OF OXALIC ACID & GLYOXYLIC ACID. IN BATCH EXPT, ZIRCONIUM OXIDE WAS CAPABLE OF BINDING 5.5 UMOL OXALIC ACID & 8 UMOL OF GLYOXYLIC ACID, G SORBENT USING 0.5 G SORBENT, L & IONIC COMPOSITION RESEMBLING THAT OF PLASMA. RECIRCULATION OF 2 L OF THE SAME SOLN THROUGH 12 G OF MIXT OF HYDROUS ZIRCONIUM OXIDE & ALUMINA FOR 6 HR AT FLOW RATE OF 12 ML, MIN, RESULTED IN FINAL CONCN OF 70 UMOL, L OF OXALIC ACID & 50 UMOL, L OF GLYOXYLIC ACID..

Which category does Glyoxylic acid monohydrate belong to?

Category: Organic Chemicals.

PubChem Public Data

Independent reference data for Glyoxylic acid monohydrate (CAS 563-96-2), compiled from public chemistry databases.

Registry identifiers across databases

CAS Registry Number563-96-2
PubChem CID760
Molecular formulaC2H2O3
IUPAC nameoxaldehydic acid
UNII (FDA)JQ39C92HH6

Computed descriptors

Molecular Weight74.04
XLogP3-0.3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass74.000393922
Monoisotopic Mass74.000393922
Topological Polar Surface Area54.4
Heavy Atom Count5

Physicochemical values on record

Melting Point98
Melting Point98 °C
Melting Point-93 °C
Density1.42 @ 20 °C/4 °C
Vapor Pressure1.06 [mmHg]
LogPlog Kow= -0.07
Dissociation Constants3.3 (at 25 °C)
Dissociation ConstantspKa = 3.30 @ 25 °C
Formulations/PreparationsSUPPLIED AS A 50% SOLN ... .

Documented uses on record

    Found in unripe fruit, young green leaves, and very young sugar beets; [Merck Index] Used to make flavorings, perfumes, cosmetics, pharmaceuticals, dyes, plastics, agricultural chemicals, and vanillin; Also used as a cleaning agent for a variety of industrial applications; [HSDB]INTERMEDIATE FOR FLAVORINGS, PERFUMES, PHARMACEUTICALS, DYES, PLASTICS, AGRICULTURAL CHEMICALS.

    Synonyms and trade names

    glyoxylic acid; 298-12-4; 2-Oxoacetic Acid; Glyoxalic acid; Oxoacetic acid; Oxoethanoic acid; Formylformic acid; Acetic acid, oxo-; Oxalaldehydic acid; oxaldehydic acid; glyoxylate; alpha-Ketoacetic acid; Formic acid, formyl-; glyoxalate; Kyselina glyoxylova; JQ39C92HH6

    GHS hazard classification

    Reported hazard statementsH317, H318, H290 (60.6%), H319

    H317: May cause an allergic skin reaction [Warning Sensitization, Skin]

    H318: Causes serious eye damage [Danger Serious eye damage/eye irritation]

    What the public record says

    Glyoxylic acid monohydrate · CAS 563-96-2 · C2H2O3. UNII JQ39C92HH6. Melting Point: 98; Melting Point: 98 °C; Melting Point: -93 °C.

    Physical description and handling notes

    Source: PubChem / Wikidata; the batch COA governs where values differ.

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