CAS 583-91-5

2-Hydroxy-4-(methylthio)butanoic acid

Description:

2-Hydroxy-4-(methylthio)butanoic acid, also known by its CAS number 583-91-5, is an organic compound characterized by the presence of a hydroxyl group (-OH) and a methylthio group (-S-CH3) attached to a butanoic acid backbone. This compound is a type of amino acid derivative, specifically a thioether, which contributes to its unique chemical properties. It is typically a white to off-white crystalline solid that is soluble in water due to the polar hydroxyl group. The presence of the methylthio group can influence its reactivity and interactions with other molecules, making it of interest in various biochemical applications. This compound may be involved in metabolic pathways and can serve as a precursor or intermediate in the synthesis of other biologically relevant molecules. Its characteristics, including melting point, boiling point, and specific reactivity, can vary based on environmental conditions and the presence of other substances. Overall, 2-Hydroxy-4-(methylthio)butanoic acid is significant in both synthetic and biological chemistry contexts.

Formula: C₅H₁₀O₃S

InChI: InChI=1S/C5H10O3S/c1-9-3-2-4(6)5(7)8/h4,6H,2-3H2,1H3,(H,7,8)

InChI key: InChIKey=ONFOSYPQQXJWGS-UHFFFAOYSA-N

SMILES: C(C(O)=O)(CCSC)O

Synonyms:

• 2-Hydroxy-4-(Methylsulfanyl)Butanoic Acid
• 2-Hydroxy-4-(methylmercapto)butyric acid
• 2-Hydroxy-4-(methylthio)butanoic acid
• 2-Hydroxy-4-Methylthiobutyric acid = DL-2-Hydroxy-4-(methylthio)butyric Acid (68-72% in Water)
• <span class="text-smallcaps">DL</span>-2-Hydroxy-4-(methylmercapto)butanoic acid
• <span class="text-smallcaps">DL</span>-2-Hydroxy-4-(methylmercapto)butyric acid
• <span class="text-smallcaps">DL</span>-2-Hydroxy-4-(methylthio)butanoic acid
• <span class="text-smallcaps">DL</span>-2-Hydroxy-4-(methylthio)butyric acid
• <span class="text-smallcaps">DL</span>-α-Hydroxy-γ-methylmercaptobutyric acid
• Alimet
• At 88
• Biox-A
• Butanoic acid, 2-hydroxy-4-(methylthio)-
• Butyric acid, 2-hydroxy-4-(methylthio)-
• Butyric acid, α-hydroxy-γ-(methylmercapto)-
• DL-2-Hydroxy-4-(methylthio)butyric acid
• Desmenidol
• Desmeninol
• Hmtba
• Hydan L
• MHA acid
• Mha-Fa
• α-Hydroxy-4-(methylthio)butyric acid
• α-Hydroxy-γ-(methylmercapto)butyric acid
• α-Hydroxy-γ-(methylthio)butyric acid
• γ-(Methylmercapto)-α-hydroxybutyric acid

2-Hydroxy-4-(methylthio)butyric Acid (65-72% in Water)

CAS: 583-91-5

Formula: C₅H₁₀O₃S

Color and Shape: White - Yellow Liquid

Molecular weight: 150.19

Ref: 3B-H0654

2-Hydroxy-4-(methylthio)butyric acid

CAS: 583-91-5

Formula: C₅H₁₀O₃S

Purity: 85%

Color and Shape: Liquid

Molecular weight: 150.1961

Ref: IN-DA003HE5

2-Hydroxy-4-(methylthio)butyric acid

CAS: 583-91-5

2-Hydroxy-4-(methylthio)butyric acid

Formula: C₅H₁₀O₃S

Purity: 85%

Color and Shape: Liquid

Molecular weight: 150.2

Ref: 54-OR80710

Desmeninol

CAS: 583-91-5

Desmeninol is an α-hydroxy methionine analogue used as a livestock feed additive and for managing protein metabolism in renal insufficiency patients.

Formula: C₅H₁₀O₃S

Color and Shape: Transparent Liquid

Molecular weight: 150.2

Ref: TM-T20705

2-Hydroxy-4-(methylthio)butyric acid

CAS: 583-91-5

2-Hydroxy-4-(methylthio)butyric acid

Formula: C₅H₁₀O₃S

Purity: 85%

Molecular weight: 150.2

Ref: IN-DG75600

2-HYDROXY-4-(METHYLTHIO)BUTYRIC ACID

CAS: 583-91-5

Purity: 88%

Color and Shape: Liquid

Molecular weight: 150.1900024

Ref: 10-F819009

DL-2-Hydroxy-4-(methylthio)butanoic acid-d3

Controlled Product

CAS: 583-91-5

Formula: C₅D₃H₇O₃S

Color and Shape: Neat

Molecular weight: 153.215

Ref: TR-H948388

2-Hydroxy-4-(methylthio)butanoic acid

CAS: 583-91-5

2-Hydroxy-4-(methylthio)butanoic acid (2HMB) is an amide that is used as a microbial metabolism inhibitor, especially for the inhibition of bacterial growth. 2HMB and its analogues are also used in plant physiology. 2HMB has been shown to have transport properties and can be used as an inorganic acid for the manufacture of hydrochloric acid. It has been found to have enzyme activities, such as polymerase chain reaction and hydroxyl group transferases, which make it a useful catalyst for reactions involving organic compounds. The hydroxyl group in 2HMB makes it a good candidate for use in fatty acid synthesis and oxidation reactions. Chronic exposure to this chemical may lead to carbonyl oxygen formation.

Formula: C₅H₁₀O₃S

Purity: Min. 95%

Color and Shape: Yellow Powder

Molecular weight: 150.2 g/mol

Ref: 3D-FH164805