L-lactate

Base Information

• Chemical Name: L-lactate
• CAS No.: 27848-80-2
• Molecular Formula: C3H4O3^.Li
• Molecular Weight: 96.0119
• Hs Code.: 29181100
• European Community (EC) Number: 248-692-5
• UNII: 435SSH7H89
• DSSTox Substance ID: DTXSID801018949
• Nikkaji Number: J555.329F
• Wikidata: Q27102013
• Mol file: 27848-80-2.mol

Synonyms:L-lactate;L-Lactate ion;(2S)-2-hydroxypropanoate;Lactate ion, L-;Lactate, (S)-;(S)-lactate;(S)-(+)-Lactate ion;L(+)-lactate;Lactic acid, ION(1-), L-;435SSH7H89;72-08-2;UNII-435SSH7H89;Propanoic acid, 2-hydroxy-, ION(1-), (2S)-;(+)-Lactate;CHEMBL507018;L-(+)-Lactate;27848-80-2;Lithium L(+)-lactate;Lithium;2o9a;(2S)-2-oxidanylpropanoate;CHEBI:16651;JVTAAEKCZFNVCJ-REOHCLBHSA-M;DTXSID801018949;BDBM50257205;AKOS040752623;A839653;A876858;Q27102013;148182-33-6

Chemical Property of L-lactate

Chemical Property:

• Appearance/Colour: white fine crystalline powder
• Melting Point: 75 °C
• Refractive Index: -14 ° (C=5, H2O)
• Boiling Point: 200 °C
• Flash Point: 109.9oC
• PSA: 60.36000
• Density: 1,325g/cm
• LogP: -1.88290
• Storage Temp.: -20°C
• Sensitive.: Hygroscopic
• Water Solubility.: almost transparency in Water
• XLogP3: 0.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 89.023869017
• Heavy Atom Count: 6
• Complexity: 53.5

Purity/Quality:

98%, ^*data from raw suppliers

L-Lactic acid lithium salt 99+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T
• Hazard Codes: T
• Statements: 23/24/25-36/37/38
• Safety Statements: 22-24/25-45-36/37/39-26

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C(=O)[O-])O
• Isomeric SMILES: C[C@@H](C(=O)[O-])O
• Uses: Useful chiral synthon, building block for depsipeptides

Technology Process of L-lactate

There total 1 articles about L-lactate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

lithium L-lactate (867-55-0,16891-53-5,27848-80-2,27848-81-3,71571-61-4,73324-21-7,77252-88-1) → lithium D-lactate (867-55-0,16891-53-5,27848-80-2,27848-81-3,71571-61-4,73324-21-7,77252-88-1)

Guidance literature:

With Carbonate buffer; Yield given; NAD⁽¹⁺⁾, L-lactate dehydrogenase (L-LDH);

Reference yield: 46.0%

ethanol (64-17-5) + lithium (S)-2-hydroxypropanoate (27848-80-2) → (S)-Ethyl lactate (687-47-8)

Guidance literature:

With sulfuric acid; In benzene; Heating;

Reference yield:

lithium (S)-2-hydroxypropanoate (27848-80-2) + benzyl alcohol (100-51-6,185532-71-2) → benzyl (S)-Lactate (56777-24-3)

Guidance literature:

With hydrogenchloride;

upstream raw materials:

lithium L-lactate

Downstream raw materials:

benzyl (S)-Lactate

(S)-Ethyl lactate

lithium hydroxypyruvate

lithium D-lactate

Refernces