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CAS 772-46-3

2-Methyl-1-phenyl-2-butanol TCI M2010

2-Methyl-1-phenyl-2-butanol TCI M2010

Chemical Identity

CAS No.
772-46-3
Formula
C11H16O
Molecular weight
164.24 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-methyl-1-phenylbutan-2-ol
SMILES
CCC(C)(CC1=CC=CC=C1)O
InChIKey
FTZBYXCNXOPJEL-UHFFFAOYSA-N
PubChem
CID 101135
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2-Methyl-1-phenyl-2-butanol is a chemical compound widely used in laboratory settings for its versatile reactivity and structural versatility. As a building block in organic chemistry, it plays a crucial role in the synthesis of complex molecules, including aromatic and heterocyclic compounds. Its hydroxyl group serves as a reactive site, enabling participation in various chemical reactions such as substitution, esterification, and redox processes. This compound is essential for researchers aiming to construct and modify molecular frameworks in both academic and industrial environments.

The compound's chemical stability, combined with its reactivity under specific conditions, makes it a preferred choice for synthetic chemists. Its mild aroma and solubility in organic solvents enhance its usability in diverse experimental setups. The high purity and clarity of the product ensure reliable and reproducible results in laboratory experiments. These characteristics make it a staple in chemical laboratories, where accuracy and consistency are paramount.

In Indonesian laboratories, 2-Methyl-1-phenyl-2-butanol is commonly used in scientific research and educational programs. It is a key component in organic chemistry courses and research projects at universities and research institutions. Its availability and reliability have made it a standard material for both teaching and advanced chemical investigations.

  • Organic synthesis applications benefit from its reactivity and structural versatility, enabling the creation of complex molecules.
  • It is ideal for esterification reactions due to its hydroxyl group, which readily participates in condensation processes.
  • Redox reactions often utilize this compound as a reducing agent, thanks to its chemical stability and controlled reactivity.
  • In aromatic compound synthesis, it serves as a building block for constructing ring structures and functional groups.
  • Educational institutions use it for teaching fundamental organic chemistry concepts and reaction mechanisms.

Brand TCI
CAS number 772-46-3
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities to meet laboratory needs
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of glass or polyethylene to prevent contamination and evaporation. Due to its solubility in organic solvents, it should be kept in a well-ventilated area to minimize exposure. General laboratory precautions include wearing appropriate personal protective equipment, such as gloves and safety goggles, when handling the material. It is important to ensure that the storage area is secure and inaccessible to unauthorized personnel. Proper labeling of containers is essential to ensure safe handling and prevent accidental use.

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