L-Leucic Acid - 10mM in DMSO , CAS No.13748-90-8

CAS: 13748-90-8 Cat. No.: L421425 Summenformel: C₆H₁₂O₃ Molekulargewicht: 132.16 Beilstein Registry Number: 3336 EG-Nummer: 237-329-6

GRADE & PURITY 10mM in DMSO

Synonyms

(+)-2-Hydroxyisocaproate | L-2-Hydroxyisocaproate | CHEBI:44510 | Pentanoic acid, 2-hydroxy-4-methyl-, (2S)- | L-2-hydroxyisocaproic acid | 429V5NT5CC | (S)-(?)-2-Hydroxyisocaproic acid | 22-oxovincaleukoblastine sulfate | (S)-2-hydroxy-4-methyl-Pentanoat

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Specifications

Synonyme

(+)-2-Hydroxyisocaproate | L-2-Hydroxyisocaproate | CHEBI:44510 | Pentanoic acid, 2-hydroxy-4-methyl-, (2S)- | L-2-hydroxyisocaproic acid | 429V5NT5CC | (S)-(?)-2-Hydroxyisocaproic acid | 22-oxovincaleukoblastine sulfate | (S)-2-hydroxy-4-methyl-Pentanoat

Spezifikationen & Reinheit

10mM in DMSO

Storage

Store at -80°C

Verschickt in

Dry ice packs + Cold packs

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

Namen und Kennungen

Pubchem Sid

528765197

Kanonisches Lächeln

CC(C)CC(C(=O)O)O

IUPAC Name

(2S)-2-hydroxy-4-methylpentanoic acid

InChIKey

LVRFTAZAXQPQHI-YFKPBYRVSA-N

INCHI

1S/C6H12O3/c1-4(2)3-5(7)6(8)9/h4-5,7H,3H2,1-2H3,(H,8,9)/t5-/m0/s1

Isomere SMILES

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

WGK Deutschland

3

Molekulargewicht

132.16

Beilstein

3336

Reaxy-Rn

1721733

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1721733&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Klasse Fatty Acyls
      • Subclass Fatty acids and conjugates

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Klasse: Fatty Acyls
• Subclass: Fatty acids and conjugates
• Intermediate Tree Nodes: Not available
• Direct Parent: Hydroxy fatty acids
• Alternative Parents: Methyl-branched fatty acids Alpha hydroxy acids and derivatives Secondary alcohols Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Branched fatty acid - Hydroxy fatty acid - Methyl-branched fatty acid - Alpha-hydroxy acid - Hydroxy acid - Secondary alcohol - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organooxygen compound - Carbonyl group - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Aliphatic acyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as hydroxy fatty acids. These are fatty acids in which the chain bears a hydroxyl group.
• External Descriptors: Hydroxy fatty acids

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

Chemische und physikalische Eigenschaften

• Spezifische Drehung [α]: -26° (C=2,NaOH sol.(1%))
• Schmelzpunkt (°C): 78-80 °C
• Molekulargewicht: 132.160 g/mol
• XLogP3: 0.900
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 132.079 Da
• Monoisotopic Mass: 132.079 Da
• Topological Polar Surface Area: 57.500 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 98.500
• 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