DL-glutamic acid
amino acid and neurotransmitter
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Summary
DL-glutamic acid is a group of stereoisomers[1]. It ranks in the top 4% of group_of_stereoisomers entities by monthly Wikipedia readership (16,582 views/month).[2]
Key Facts
- DL-glutamic acid's instance of is recorded as group of stereoisomers[3].
- DL-glutamic acid's canonical SMILES is recorded as C(CC(=O)O)C(C(=O)O)N[4].
- DL-glutamic acid's chemical formula is recorded as C₅H₉NO₄[5].
- DL-glutamic acid is a type of alpha-amino acid[6].
- DL-glutamic acid is a type of dicarboxylic acid[7].
- DL-glutamic acid is part of anaerobic glutamate catabolic process[8].
- DL-glutamic acid is used for food additive[9].
- DL-glutamic acid's Commons category is recorded as Glutamic acid[10].
- DL-glutamic acid comprises nitrogen[11].
- DL-glutamic acid comprises carbon[12].
- DL-glutamic acid's found in taxon is recorded as Pisum sativum[13].
- DL-glutamic acid's found in taxon is recorded as Trifolium pratense[14].
- DL-glutamic acid's found in taxon is recorded as Trifolium repens[15].
- DL-glutamic acid's found in taxon is recorded as Streptomyces coelicolor[16].
- DL-glutamic acid's found in taxon is recorded as Streptomyces albidoflavus[17].
- DL-glutamic acid's found in taxon is recorded as Caenorhabditis elegans[18].
- DL-glutamic acid's pKa is recorded as {'amount': '+4.07'}[19].
- DL-glutamic acid's described by source is recorded as Armenian Soviet Encyclopedia, vol. 3[20].
- DL-glutamic acid's described by source is recorded as Otto's encyclopedia[21].
- DL-glutamic acid's MCN code is recorded as 2922.42.10[22].
- DL-glutamic acid's mass is recorded as {'unit': 'dalton', 'amount': '+147.053'}[23].
- DL-glutamic acid's melting point is recorded as {'unit': 'degree Celsius', 'amount': '+160'}[24].
- DL-glutamic acid's boiling point is recorded as {'unit': 'degree Celsius', 'amount': '+205'}[25].
- DL-glutamic acid's decomposition point is recorded as {'unit': 'degree Celsius', 'amount': '+205'}[26].
- DL-glutamic acid's safety classification and labelling is recorded as NFPA 704: Standard System for the Identification of the Hazards of Materials for Emergency Response[27].
Why It Matters
DL-glutamic acid ranks in the top 4% of group_of_stereoisomers entities by monthly Wikipedia readership (16,582 views/month).[2] It has Wikipedia articles in 30 language editions, a strong signal of global cultural recognition.[28] It is known by 105 alternative names across languages and contexts.[29]