Glyoxylic acid
PubChem CID: 760
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| Compound Synonyms | glyoxylic acid, 298-12-4, 2-Oxoacetic Acid, Glyoxalic acid, Oxoacetic acid, Oxoethanoic acid, Formylformic acid, Acetic acid, oxo-, Oxalaldehydic acid, alpha-Ketoacetic acid, oxaldehydic acid, Formic acid, formyl-, Acetic acid, 2-oxo-, Kyselina glyoxylova, glyoxalate, CCRIS 1455, HSDB 5559, Kyselina glyoxylova [Czech], NSC 27785, Glyoxalsaeure, Glyoxylsaeure, Acetic acid, oxo, EINECS 206-058-5, Formic acid, formyl, BRN 0741891, JQ39C92HH6, CHEBI:16891, .alpha.-Ketoacetic acid, MFCD00006958, NSC-27785, GLYOXYLIC ACID [MI], GLYOXYLIC ACID [HSDB], DTXSID5021594, GLYOXYLIC ACID [WHO-DD], EC 206-058-5, glyox, oxoacetate, 4-03-00-01489 (Beilstein Handbook Reference), NSC27785, 2-OxoaceticAcid, 2-Oxoacetate, ALLANTOIN IMPURITY A [EP IMPURITY], GLYOXALATE, GLYOXYLATE, Glyoxalic acid pound 50% in water pound(c), NSC 27785, Formylformic acid, Oxalaldehydic acid, GLV, ALLANTOIN IMPURITY A (EP IMPURITY), OCHCOOH, UNII-JQ39C92HH6, Formylformate, Oxalaldehydate, Oxoethanoate, alpha-ketoester, glyoxilic acid, a-Ketoacetate, alpha-ketoesters, C2H2O3, alpha-keto ester, alpha-keto-ester, alpha-Ketoacetate, (oxo)acetic acid, a-Ketoacetic acid, alphaKetoacetic acid, OHCCO2H, Glyoxylic acid (8CI), Glyoxylic acid anhydrous, WLN: VHVQ, dioxymethylene formaldehyde, Glyoxalic acid (Standard), Acetic acid, oxo- (9CI), GLYOXALATE, GLYOXYLATE, GLYOXYLIC ACID [INCI], DTXCID401594, Glyoxylic acid, 50% in water, CHEMBL1162545, BDBM19472, CHEBI:51848, Glyoxylic acid (50% in water), STR06186, Glyoxylic acid, 50% w/w aq. soln, HY-79494R, STL168883, AKOS005367012, CS-W019807, DB04343, FG01566, Glyoxylic acid - 50% aqueous solution, HY-79494, 2-OXOACETIC ACID (50% IN WATER), G0366, NS00003540, EN300-20485, C00048, D70821, Q413552, F2191-0150, 0ADD8E81-5E77-4171-9241-E74AC05D4C8D, 206-058-5 |
|---|---|
| Ghose Rule | False |
| Classyfire Kingdom | Organic compounds |
| Topological Polar Surface Area | 54.4 |
| Hydrogen Bond Donor Count | 1.0 |
| Pfizer 3 75 Rule | False |
| Deep Smiles | O=CC=O)O |
| Heavy Atom Count | 5.0 |
| Classyfire Class | Carboxylic acids and derivatives |
| Description | Glyoxylic acid, also known as alpha-ketoacetic acid or glyoxylate, is a member of the class of compounds known as carboxylic acids. Carboxylic acids are compounds containing a carboxylic acid group with the formula -C(=O)OH. Glyoxylic acid is soluble (in water) and a moderately acidic compound (based on its pKa). Glyoxylic acid can be found in a number of food items such as european chestnut, cowpea, wheat, and common thyme, which makes glyoxylic acid a potential biomarker for the consumption of these food products. Glyoxylic acid can be found primarily in blood, cerebrospinal fluid (CSF), feces, and urine, as well as throughout all human tissues. Glyoxylic acid exists in all living species, ranging from bacteria to humans. In humans, glyoxylic acid is involved in a couple of metabolic pathways, which include alanine metabolism and glycine and serine metabolism. Glyoxylic acid is also involved in several metabolic disorders, some of which include lactic acidemia, pyruvate carboxylase deficiency, 3-phosphoglycerate dehydrogenase deficiency, and hyperglycinemia, non-ketotic. Moreover, glyoxylic acid is found to be associated with transurethral resection of the prostate and primary hyperoxaluria I. Glyoxylic acid or oxoacetic acid is an organic compound. Together with acetic acid, glycolic acid, and oxalic acid, glyoxylic acid is one of the C2 carboxylic acids. It is a colourless solid that occurs naturally and is useful industrially . |
| Classyfire Subclass | Carboxylic acids |
| Isotope Atom Count | 0.0 |
| Molecular Complexity | 55.9 |
| Database Name | fooddb_chem_all;hmdb_chem_all;imppat_phytochem;npass_chem_all;pubchem |
| Defined Atom Stereocenter Count | 0.0 |
| Uniprot Id | P14920, P19021, Q9UBQ7, Q9BYV1, Q9UJM8, Q9NYQ3, P21549, O15427, Q6YP21, Q86XE5, P0A6L2 |
| Iupac Name | oxaldehydic acid |
| Class | Carboxylic acids and derivatives |
| Veber Rule | True |
| Classyfire Superclass | Organic acids and derivatives |
| Xlogp | -0.3 |
| Superclass | Organic acids and derivatives |
| Subclass | Carboxylic acids |
| Gsk 4 400 Rule | True |
| Molecular Formula | C2H2O3 |
| Inchi Key | HHLFWLYXYJOTON-UHFFFAOYSA-N |
| Silicos It Class | Soluble |
| Rotatable Bond Count | 1.0 |
| State | Liquid |
| Synonyms | alpha-Ketoacetic acid, Formylformic acid, Glyoxalate, Glyoxalsaeure, Glyoxylate, Glyoxylsaeure, Oxalaldehydic acid, Oxoethanoic acid, a-Ketoacetate, a-Ketoacetic acid, alpha-Ketoacetate, Α-ketoacetate, Α-ketoacetic acid, Formylformate, Glyoxalic acid, Oxalaldehydate, Oxoethanoate, Oxoacetate, Oxoacetic acid, Glyoxylic acid, 2-(14)C-labeled, Glyoxylic acid, sodium salt, Glyoxylic acid, sodium salt, 2-(14)C-labeled, Glyoxylic acid, 14c2-labeled, Glyoxylic acid, calcium salt, Glyoxylic acid, sodium salt, 14C-labeled, glyoxalic acid |
| Esol Class | Very soluble |
| Functional Groups | O=CC(=O)O |
| Compound Name | Glyoxylic acid |
| Kingdom | Organic compounds |
| Exact Mass | 74.0004 |
| Formal Charge | 0.0 |
| Monoisotopic Mass | 74.0004 |
| Hydrogen Bond Acceptor Count | 3.0 |
| Molecular Weight | 74.04 |
| Gi Absorption | True |
| Covalent Unit Count | 1.0 |
| Total Atom Stereocenter Count | 0.0 |
| Total Bond Stereocenter Count | 0.0 |
| Molecular Framework | Aliphatic acyclic compounds |
| Lipinski Rule Of 5 | True |
| Inchi | InChI=1S/C2H2O3/c3-1-2(4)5/h1H,(H,4,5) |
| Smiles | C(=O)C(=O)O |
| Defined Bond Stereocenter Count | 0.0 |
| Egan Rule | True |
| Taxonomy Direct Parent | Carboxylic acids |
- 1. Outgoing r'ship
FOUND_INto/from Euphorbia Hirta (Plant) Rel Props:Reference:ISBN:9788172360818 - 2. Outgoing r'ship
FOUND_INto/from Tamarindus Indica (Plant) Rel Props:Source_db:fooddb_chem_all