L-Lactic Acid - Moligand™, ≥98%(T) , CAS No.79-33-4

CAS: 79-33-4 Cat. No.: L118493 Summenformel: C₃H₆O₃ Molekulargewicht: 90.08 Beilstein Registry Number: 1720251 EG-Nummer: 201-196-2

QUALITÄT & REINHEIT Moligand™, ≥98%(T)

Synonyms

L-Milchsaeure | (S)-2-Hydroxypropanoate | (S)-2-hydroxy-Propanoate | (S)-LACTIC ACID (EP MONOGRAPH) | 1-Hydroxyethane 1-carboxylate | DTXSID6034689 | L-(+)-Lactic acid solution | L-(+)-Lactic acid, 80% | F9S9FFU82N | L-lactate | L-(+)-alpha-Hydroxypropion

Storage

Protected from light,Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Übersicht

Usually used as a substrate for lactic acid dehydrogenase and lactate oxidase.

L-(+)-Lactic acid is the only naturally occurring lactic acid in humans and mammals. Commercially, few bacteria like Lactobacillus casei, L. delbrueckii, Streptococcus lactis produces L-Lactic acid by fermentation process. Lactic acid activates hydroxycarboxylic acid receptor, G-protein coupled receptor 81 (GPR81).

Spezifikationen

Synonyme

L-Milchsaeure | (S)-2-Hydroxypropanoate | (S)-2-hydroxy-Propanoate | (S)-LACTIC ACID (EP MONOGRAPH) | 1-Hydroxyethane 1-carboxylate | DTXSID6034689 | L-(+)-Lactic acid solution | L-(+)-Lactic acid, 80% | F9S9FFU82N | L-lactate | L-(+)-alpha-Hydroxypropion

Spezifikationen & Reinheit

Moligand™, ≥98%(T)

Biochemische und physiologische Mechanismen

L-(+)-Lactic acid is used as a substrate for lactic acid dehydrogenase and lactate oxidase.

Storage

Protected from light,Store at -20°C,Argon charged

Verschickt in

Ice chest + Ice pads

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Note

Moligand™

Reinheit

≥98%(T)

Namen und Kennungen

Pubchem Sid

508810629

Kanonisches Lächeln

C[C@H](O)C(O)=O

IUPAC Name

(2S)-2-hydroxypropanoic acid

InChIKey

JVTAAEKCZFNVCJ-REOHCLBHSA-N

INCHI

1S/C3H6O3/c1-2(4)3(5)6/h2,4H,1H3,(H,5,6)/t2-/m0/s1

Isomere SMILES

C[C@@H](C(=O)O)O

WGK Deutschland

1

RTECS

OD2800000

UN-Nummer

3265

Verpackungsgruppe

III

Molekulargewicht

90.08

Beilstein

1720251

Reaxy-Rn

1720251

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1720251&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Klasse Hydroxy acids and derivatives
      • Subclass Alpha hydroxy acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: Hydroxy acids and derivatives
• Subclass: Alpha hydroxy acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Alpha hydroxy acids and derivatives
• Alternative Parents: Secondary alcohols Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alpha-hydroxy acid - Secondary alcohol - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as alpha hydroxy acids and derivatives. These are organic compounds containing a carboxylic acid substituted with a hydroxyl group on the adjacent carbon.
• External Descriptors: 2-hydroxypropanoic acid

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

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HCAR1 Tchem Hydroxycarboxylic acid receptor 1 (0 Activities)

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MRC5 (9203 Activities)

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A549 (127892 Activities)

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SLC16A1 Tchem Monocarboxylate transporter 1 (146 Activities)

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SLC16A3 Tchem Monocarboxylate transporter 4 (196 Activities)

Discover Target: SLC16A3

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SLC16A7 Tchem Monocarboxylate transporter 2 (11 Activities)

Discover Target: SLC16A7

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SARS-CoV-2 (38078 Activities)

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Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Löslichkeit: Soluble in water (100 mg/ml), alcohol, acetone, and methanol. Insoluble in chloroform, petroleum, ether, and carbon disulfide.
• Empfindlichkeit: Moisture & Light sensitive
• Brechungsindex: 1.4260 to 1.4310
• Spezifische Drehung [α]: -10.0 to -15.0 deg(C=2.5, 1.5mol/L NaOH sol.)
• Flammpunkt (°C): 110 °C
• Siedepunkt (°C): 122 °C/20 hPa
• Schmelzpunkt (°C): 18 °C
• Molekulargewicht: 90.080 g/mol
• XLogP3: -0.700
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 90.0317 Da
• Monoisotopic Mass: 90.0317 Da
• Topological Polar Surface Area: 57.500 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 59.100
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1