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TCI

CAS 513-42-8

beta-Methallyl Alcohol TCI M0091

beta-Methallyl Alcohol TCI M0091

Chemical Identity

CAS No.
513-42-8
PubChem
CID 10557·SID 87572202
Formula
C4H8O
Molecular weight
72.11 g/mol
Purity
>98.0%(GC)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-methylprop-2-en-1-ol
SMILES
CC(=C)CO
InChIKey
BYDRTKVGBRTTIT-UHFFFAOYSA-N
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Beta-Methallyl Alcohol is an organic compound widely utilized in chemical reactions for the synthesis of complex molecules. It serves as a fundamental building block in both heterocyclic and non-heterocyclic compound preparations. In laboratory settings, this compound acts as a precursor in various reactions such as hydroxylation, esterification, and substitution reactions. Its molecular structure is simple yet highly reactive, enabling it to participate effectively in diverse chemical processes.

The compound's polarity and solubility in organic solvents make it a versatile reagent for different reaction conditions. These properties contribute to its efficiency in forming new compounds with high yield. Its reactivity and compatibility with various chemical environments make it a preferred choice for researchers aiming to achieve precise and efficient synthetic outcomes.

In Indonesian laboratories, Beta-Methallyl Alcohol is commonly used in organic chemistry research, particularly in the development of pharmaceutical compounds and industrial chemicals. Its availability in various chemical products makes it a frequently sought-after material among researchers and laboratory professionals. The compound plays a crucial role in advancing chemical synthesis and innovation in both academic and industrial contexts.

  • Synthesis of heterocyclic compounds for pharmaceutical development due to its reactivity and compatibility with various reaction conditions.
  • Organic chemistry research where efficient and high-yield synthesis of complex molecules is required.
  • Industrial chemical production for the creation of specialized compounds used in multiple sectors.
  • Development of new drug compounds through controlled chemical reactions that benefit from Beta-Methallyl Alcohol’s structural versatility.
  • Chemical process optimization where the compound’s solubility and reactivity aid in achieving desired product outcomes.

Brand TCI
CAS number 513-42-8
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities as per supplier specifications
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight and incompatible materials

Beta-Methallyl Alcohol should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in a tightly sealed container to prevent evaporation and contamination. Due to its reactivity, it should be stored separately from strong oxidizing agents and incompatible substances. Proper ventilation is essential when handling the compound to minimize exposure. Laboratory personnel should use appropriate personal protective equipment, including gloves and safety goggles, to ensure safe handling. Regular inspection of storage conditions is advised to maintain the integrity and safety of the compound.

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