DL-Valine

1. Defined Racemic Composition: DL-Valine contains both D- and L-valine forms, making it suitable for applications that require the racemic amino acid rather than a single enantiomer.

2. Verified Chemical Identity: Its CAS number, molecular formula, and molecular weight provide clear reference points for material identification and incoming quality checks.

3. Functional Amino and Carboxyl Groups: The molecule contains an amino group and a carboxyl group, allowing it to participate in selected chemical reactions and amino acid research.

4. Flexible Research and Synthesis Use: It can be selected for laboratory studies, analytical work, and specific synthesis processes when a racemic valine material is required.

Product Description

DL-Valine (CAS 516-06-3) is a racemic form of valine, an alpha-amino acid with the molecular formula C₅H₁₁NO₂ and a molecular weight of approximately 117.15 g/mol. Its structure includes an amino group, a carboxyl group, and a branched isopropyl side chain. Unlike L-valine or D-valine supplied as a single stereoisomer, DL-valine contains both enantiomeric forms.

This stereochemical distinction is important when selecting amino acid materials for research, analytical procedures, or chemical synthesis. The presence of both enantiomers can affect the outcome of experiments and processes that are sensitive to chirality, so the specified stereochemical composition should be checked before use.

DL-Valine is generally supplied as a white crystalline powder. Actual appearance, assay, moisture content, and impurity limits depend on the supplied grade and production specification. Buyers should confirm the intended application, required purity, particle characteristics if relevant, packaging, and storage conditions before placing an order. For pharmaceutical, food, or other regulated uses, verify that the particular grade is suitable under the applicable requirements.

DL-Valine CAS#516-06-3

Chemical Properties

PropertyDetails
Product NameDL-Valine
CAS Number516-06-3
Molecular FormulaC₅H₁₁NO₂
Molecular Weight117.15 g/mol
IUPAC Name2-Amino-3-methylbutanoic acid
SynonymsDL-α-Aminoisovaleric Acid; DL-2-Aminoisovaleric Acid; Valine, DL-
Chemical CategoryRacemic Alpha-Amino Acid
StereochemistryRacemic mixture of D- and L-valine
AppearanceTypically a white crystalline powder
Functional GroupsAmino group and carboxyl group
SolubilitySoluble in water; exact solubility depends on test conditions
StorageStore in a tightly closed container in a cool, dry place according to the supplied SDS and product label

Product Applications

1. Amino Acid Research

Used in studies investigating amino acid structure, stereochemistry, and the behavior of racemic compounds. Its mixed enantiomeric composition makes it relevant to experiments that compare racemic and optically defined materials.

2. Chiral Analysis and Method Development

Can be used in analytical method development for evaluating enantiomer separation, amino acid identification, and stereochemical composition.

3. Chemical Synthesis

Serves as a starting material or reagent in selected synthesis routes where a racemic valine structure is required. Suitability depends on the reaction pathway and the required stereochemical outcome.

4. Biochemical and Laboratory Studies

Used in laboratory investigations involving amino acid chemistry, molecular interactions, and related analytical procedures.

5. Reference and Quality-Control Work

May be used as a test material in suitable analytical workflows. For quantitative calibration or regulated testing, use material with documentation and reference status appropriate to the method.

DL-Valine CAS#516-06-3

FAQ

Q1: What is the CAS number of DL-Valine?

A: The CAS number is 516-06-3.

Q2: What are the molecular formula and molecular weight of DL-Valine?

A: The molecular formula is C₅H₁₁NO₂, and the molecular weight is approximately 117.15 g/mol.

Q3: How does DL-Valine differ from L-Valine?

A: DL-Valine is a racemic mixture containing D- and L-valine, while L-Valine refers to one specific enantiomer. They should not be treated as interchangeable in stereochemistry-sensitive applications.

Q4: Is DL-Valine suitable for chiral analysis?

A: It can be used in suitable analytical method development and studies involving enantiomer separation. Confirm the material specification and analytical method requirements before use.

Q5: What should be checked before purchasing DL-Valine?

A: Confirm the CAS number, assay, stereochemical composition, moisture content, impurity limits, packaging, and intended use. Request the current technical data sheet, batch-specific certificate of analysis, and safety data sheet.

Q6: Can DL-Valine be used in pharmaceutical or food applications?

A: Suitability depends on the specific grade, intended use, and applicable regulations. Confirm the required quality standard and regulatory status before using it in a regulated product.

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