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

CAS: 79-33-4 Cat. No.: L118493 Formula: C₃H₆O₃ Peso molecolare: 90.08 Beilstein Registry Number: 1720251 Numero EC: 201-196-2

QUALITÀ & PUREZZA 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

Panoramica

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).

Specifiche

Sinonimi

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

Specifiche e purezza

Moligand™, ≥98%(T)

Meccanismi biochimici e fisiologici

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

Condizioni di conservazione di stoccaggio

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

Spedito in

Ice chest + Ice pads

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Grado

Moligand™

Purezza

≥98%(T)

Nomi e identificatori

Pubchem Sid

508810629

Sorrisi canonici

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

Isomeri SMILES

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

WGK Germania

1

RTECS

OD2800000

Numero UN

3265

Gruppo di imballaggio

III

Peso molecolare

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
    • Classe Hydroxy acids and derivatives
      • Subclass Alpha hydroxy acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: 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
• Descrizione: 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

Obiettivi associati (umani)

HCAR1 Tchem Hydroxycarboxylic acid receptor 1 (0 Activities)

Discover Target: HCAR1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

MRC5 (9203 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

A549 (127892 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC16A1 Tchem Monocarboxylate transporter 1 (146 Activities)

Discover Target: SLC16A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC16A3 Tchem Monocarboxylate transporter 4 (196 Activities)

Discover Target: SLC16A3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC16A7 Tchem Monocarboxylate transporter 2 (11 Activities)

Discover Target: SLC16A7

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Obiettivi associati (non umani)

SARS-CoV-2 (38078 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Soluble in water (100 mg/ml), alcohol, acetone, and methanol. Insoluble in chloroform, petroleum, ether, and carbon disulfide.
• Sensibilità: Moisture & Light sensitive
• Indice di rifrazione: 1.4260 to 1.4310
• Rotazione specifica [α]: -10.0 to -15.0 deg(C=2.5, 1.5mol/L NaOH sol.)
• Punto di infiammabilità (°C): 110 °C
• Punto di ebollizione (°C): 122 °C/20 hPa
• Punto di fusione (°C): 18 °C
• Peso molecolare: 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