Lactic Acid, L-
PubChem CID: 107689
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| Compound Synonyms | L-Lactic acid, 79-33-4, L-(+)-Lactic acid, (S)-Lactic acid, (S)-2-Hydroxypropanoic acid, Sarcolactic acid, (2S)-2-hydroxypropanoic acid, (+)-Lactic acid, (S)-2-Hydroxypropionic acid, L(+)-LACTIC ACID, Paralactic acid, (S)-(+)-Lactic acid, Lactic acid, L-, Tisulac, PURAC, Paramilchsaeure, Fleischmilchsaeure, (S)-Milchsaeure, (S)-lactate, Acidum sarcolacticum, Sarcolacticum acidum, L-lactate, Propanoic acid, 2-hydroxy-, (2S)-, Pleo sanvis, PH 90, (S)-2-Hydroxypropionsaeure, L-(+)-alpha-Hydroxypropionic acid, L-Milchsaeure, UNII-F9S9FFU82N, PROPANOIC ACID, 2-HYDROXY-, (S)-, EINECS 201-196-2, F9S9FFU82N, CHEBI:422, L(+)-2-Hydroxypropionsaeure, BRN 1720251, L-Lactic Acid, 90%, DEXTROROTATORY LACTIC ACID, EC 201-196-2, 4-03-00-00633 (Beilstein Handbook Reference), l-milchsaure, (+)-Lactate, MFCD00064266, (S)-LACTIC ACID (EP MONOGRAPH), (S)-LACTIC ACID [EP MONOGRAPH], PLLA, S-Lactic acid, (S)-2-hydroxypropanoic acid, 1-Hydroxyethane 1-carboxylic acid, L-lacticacid, Lactisan Winter, Pleo Sanuvis, (alpha)-Lactate, L-Iactic acid, L Lactic Acid, a-Hydroxypropanoate, a-Hydroxypropionate, 26811-96-1, 2OP, ClO2-C Activator, nchembio867-comp9, (alpha)-Lactic acid, alpha-Hydroxypropanoate, alpha-Hydroxypropionate, L-2-Hydroxypropanoate, a-Hydroxypropanoic acid, a-Hydroxypropionic acid, L-(+) Lactic Acid, (S)-2-Hydroxypropanoate, (S)-2-Hydroxypropionate, 1-Hydroxyethanecarboxylate, L-Lactic acid, anhydrous, L-2-Hydroxypropanoic acid, L-Lactic acid (Standard), L-Lactic acid - 98%, bmse000208, bmse000818, bmse000979, D-Lactic Acid (90%), (S)-2-hydroxy-Propanoate, (?)-LACTATE, L-LACTIC ACID [MI], L-LACTIC ACID (+), L-LACTIC ACID [JAN], L-(+)-Lactic acid solution, 1-Hydroxyethane 1-carboxylate, LACTIC ACID, L-(II), (S)-2-hydroxy-Propanoic acid, (S)-2-hydroxy-propionic acid, CHEMBL330546, GTPL2932, L- LACTIC ACID (+), (S)-(+)-2-Hydroxypropanoate, L-(+)-Lactic acid, 80%, (S)(+)2 hydroxypropionic acid, DTXSID6034689, LACTIC ACID, L- [II], HY-Y0479R, (s)(+)-2 hydroxypropionic acid, L-Lactic acid, solution, 85%+, SARCOLACTIC ACID [WHO-DD], L-(+)-Lactic acid 95% liquid, 80% (w/w) Lactic Acid Solution, L-(+)-Lactic acid solution, 1M, L-(+)-Lactic acid, >=98%, SARCOLACTICUM ACIDUM [HPUS], (S)-(+)-2-Hydroxypropanoic acid, 2-Hydroxypropanoic acid, (S)- #, HY-Y0479, s6250, AKOS025146504, DB14475, L-(+)-Lactic acid, analytical standard, FL162669, FL168668, CS-0015266, L0165, NS00006010, EN300-91905, C00186, D71144, G64463, L-(+)-Lactic acid, BioXtra, >=98% (titration), L-(+)-Lactic acid, Vetec(TM) reagent grade, 86%, Q27080955, 5E39D33D-2F71-4C24-BC7A-5E6F27E4CF83, L+Lactic Acid, Free Acid (S)-2-Hydroxypropionic acid, Sarcolactic acid, 201-196-2 |
|---|---|
| Topological Polar Surface Area | 57.5 |
| Hydrogen Bond Donor Count | 2.0 |
| Heavy Atom Count | 6.0 |
| Pathway Kegg Map Id | map00620, map00010 |
| Description | Widely distributed in nature - starch, molasses, potatoes etc. Lactic acid is chiral and has two optical isomers. One is known as L-(+)-lactic acid or (S)-lactic acid and the other, its mirror image, is D-(-)-lactic acid or (R)-lactic acid. L-(+)-Lactic acid is the biologically important isomer. D-Lactic acid is found in many foods, some of which are allium (onion), pistachio, common walnut, and common thyme. |
| Isotope Atom Count | 0.0 |
| Molecular Complexity | 59.1 |
| Database Name | cmaup_ingredients;fooddb_chem_all;hmdb_chem_all;npass_chem_all;pubchem |
| Defined Atom Stereocenter Count | 1.0 |
| Uniprot Id | Q6ZMR3, P07195, P07864, P00338, Q9BYZ2, P53987, n.a. |
| Iupac Name | (2S)-2-hydroxypropanoic acid |
| Prediction Hob | 1.0 |
| Class | Hydroxy acids and derivatives |
| Xlogp | -0.7 |
| Superclass | Organic acids and derivatives |
| Subclass | Alpha hydroxy acids and derivatives |
| Molecular Formula | C3H6O3 |
| Prediction Swissadme | 0.0 |
| Inchi Key | JVTAAEKCZFNVCJ-REOHCLBHSA-N |
| Fcsp3 | 0.6666666666666666 |
| Rotatable Bond Count | 1.0 |
| State | Solid |
| Synonyms | (-)-Lactate, (-)-Lactic acid, (2R)-2-Hydroxypropanoic acid, (D)-(-)-Lactic acid, (R)-(-)-Lactate, (R)-(-)-Lactic acid, (R)-2-Hydroxypropanoate, (R)-2-Hydroxypropanoic acid, (R)-2-Hydroxypropionate, (R)-2-Hydroxypropionic acid, (R)-a-Hydroxypropionate, (R)-a-Hydroxypropionic acid, (R)-alpha-Hydroxypropionate, (R)-alpha-Hydroxypropionic acid, (R)-Lactate, (R)-Lactic acid, 2-Hydroxypropanoic acid, 9CI, D-form, D-(-)-Lactate, D-(-)-Lactic acid, D-2-Hydroxypropanoate, D-2-Hydroxypropanoic acid, D-2-Hydroxypropionate, D-2-Hydroxypropionic acid, D-Lactate, D-Lactic acid, D-Milchsaeure, delta-(-)-Lactate, delta-(-)-Lactic acid, delta-2-Hydroxypropanoate, delta-2-Hydroxypropanoic acid, delta-2-Hydroxypropionate, delta-2-Hydroxypropionic acid, delta-Lactate, delta-Lactic acid, DLA, L-(+)-Lactate, LACTIC ACID, Propanoic acid, 2-hydroxy-, (2R)-, Propanoic acid, 2-hydroxy-, (R)-, Propel, (+)-Lactate, (+)-Lactic acid, (2S)-2-Hydroxypropanoic acid, (alpha)-Lactate, (alpha)-Lactic acid, (S)-(+)-2-Hydroxypropanoate, (S)-(+)-2-Hydroxypropanoic acid, (S)-(+)-Lactate, (S)-(+)-Lactic acid, (S)-2-Hydroxy-propanoate, (S)-2-Hydroxy-propanoic acid, (S)-2-Hydroxypropanoate, (S)-2-Hydroxypropanoic acid, (S)-2-Hydroxypropionate, (S)-2-Hydroxypropionic acid, (S)-Lactate, (S)-Lactic acid, 1-Hydroxyethane 1-carboxylate, 1-Hydroxyethanecarboxylate, 2-Hydroxypropanoate, 2-Hydroxypropanoic acid, 2-Hydroxypropanoic acid, 9CI, L-form, 2-Hydroxypropionate, a-Hydroxypropanoate, a-Hydroxypropanoic acid, a-Hydroxypropionate, a-Hydroxypropionic acid, alpha-Hydroxypropanoate, alpha-Hydroxypropionate, Espiritin, L-(+)- Lactic acid, L-(+)-a-Hydroxypropionate, L-(+)-a-Hydroxypropionic acid, L-(+)-alpha-Hydroxypropionate, L-(+)-alpha-Hydroxypropionic acid, L-(+)-Lactic acid, L-(+)-α-hydroxypropionate, L-(+)-α-hydroxypropionic acid, L-2-Hydroxypropanoate, L-2-Hydroxypropanoic acid, L-Lactate, L-Lactic acid, L-Milchsaeure, Milk acid, Paralactic acid, Propanoic acid, 2-hydroxy-, (S)- (9CI), Sarcolactic acid, Tisulac, L-(+)-Α-hydroxypropionate, L-(+)-Α-hydroxypropionic acid, 1-Hydroxyethane 1-carboxylic acid, 1-Hydroxyethanecarboxylic acid, alpha-Hydroxypropanoic acid, alpha-Hydroxypropionic acid, Lactate, Lactic acid, 2-Hydroxypropionic acid, D Lactic acid, Lactate, ammonium, 2 Hydroxypropanoic acid, 2 Hydroxypropionic acid, Ammonium lactate, L Lactic acid |
| Substituent Name | Alpha-hydroxy acid, Secondary alcohol, Monocarboxylic acid or derivatives, Carboxylic acid, Carboxylic acid derivative, Hydrocarbon derivative, Organooxygen compound, Carbonyl group, Alcohol, Aliphatic acyclic compound |
| Compound Name | Lactic Acid, L- |
| Kingdom | Organic compounds |
| Prediction Hob Swissadme | 0.0 |
| Exact Mass | 90.0317 |
| Formal Charge | 0.0 |
| Monoisotopic Mass | 90.0317 |
| Hydrogen Bond Acceptor Count | 3.0 |
| Molecular Weight | 90.08 |
| Covalent Unit Count | 1.0 |
| Total Atom Stereocenter Count | 1.0 |
| Total Bond Stereocenter Count | 0.0 |
| Molecular Framework | Aliphatic acyclic compounds |
| Esol | 0.12111640000000018 |
| Inchi | InChI=1S/C3H6O3/c1-2(4)3(5)6/h2,4H,1H3,(H,5,6)/t2-/m0/s1 |
| Smiles | C[C@@H](C(=O)O)O |
| Defined Bond Stereocenter Count | 0.0 |
| Taxonomy Direct Parent | Alpha hydroxy acids and derivatives |
- 1. Outgoing r'ship
FOUND_INto/from Aloe Africana (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all - 2. Outgoing r'ship
FOUND_INto/from Aloe Barbadensis (Plant) Rel Props:Source_db:npass_chem_all - 3. Outgoing r'ship
FOUND_INto/from Aloe Ferox (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all - 4. Outgoing r'ship
FOUND_INto/from Aloe Spicata (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all - 5. Outgoing r'ship
FOUND_INto/from Aloe Vera (Plant) Rel Props:Source_db:cmaup_ingredients - 6. Outgoing r'ship
FOUND_INto/from Digitalis Purpurea (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all - 7. Outgoing r'ship
FOUND_INto/from Pogostemon Cablin (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all - 8. Outgoing r'ship
FOUND_INto/from Prunus Mume (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all - 9. Outgoing r'ship
FOUND_INto/from Typha Latifolia (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all