L-Lactic Acid - Moligand™, ACS, ≥85% , CAS No.79-33-4

CAS: 79-33-4 Cat. No.: L122089 Formule: C₃H₆O₃ Poids moléculaire: 90.08 Beilstein Registry Number: 1720251 Numéro CE: 201-196-2

QUALITÉ & PURETÉ Moligand™, ACS, ≥85%

Synonyms

L-(+)-Lactic acid, BioXtra, >=98% (titration) | L-Milchsaeure | (S)-2-Hydroxypropanoate | (S)-2-hydroxy-Propanoate | (S)-LACTIC ACID (EP MONOGRAPH) | L-(+)-Lactic acid 95% liquid | LACTIC ACID, L-(II) | (S)-LACTIC ACID [EP MONOGRAPH] | 1-Hydroxyethane 1-c

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Vue d’ensemble

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

Spécifications

Synonymes

L-(+)-Lactic acid, BioXtra, >=98% (titration) | L-Milchsaeure | (S)-2-Hydroxypropanoate | (S)-2-hydroxy-Propanoate | (S)-LACTIC ACID (EP MONOGRAPH) | L-(+)-Lactic acid 95% liquid | LACTIC ACID, L-(II) | (S)-LACTIC ACID [EP MONOGRAPH] | 1-Hydroxyethane 1-c

Spécifications et pureté

Moligand™, ACS, ≥85%

Conditions de stockage de stockage

Store at 2-8°C,Argon charged

Expédié en

Wet ice

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Grade

ACS, Moligand™

Pureté

≥85%

Noms et identifiants

Pubchem Sid

508810633

Sourires canoniques

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

Isomères SMILES

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

WGK Allemagne

1

RTECS

OD2800000

Numéro ONU

3265

Groupe d'emballage

III

Poids moléculaire

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
• Description: 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

Cibles associées (humaines)

HCAR1 Tchem Hydroxycarboxylic acid receptor 1 (0 Activities)

Discover Target: HCAR1

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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)

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

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Cibles associées (non humaines)

SARS-CoV-2 (38078 Activities)

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Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: Soluble in water (100 mg/ml), alcohol, acetone, and methanol. Insoluble in chloroform, petroleum, ether, and carbon disulfide.
• Sensibilité: Moisture & Light sensitive
• Indice de réfraction: 1.4260 to 1.4310
• Rotation spécifique [α]: -10.0 to -15.0 deg(C=2.5, 1.5mol/L NaOH sol.)
• Point d'éclair (°C): 110 °C
• Point d'ébullition (°C): 122 °C/20 hPa
• Point de fusion (°C): 18 °C
• Poids moléculaire: 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