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TCI

CAS 26537-19-9

Methyl 4-tert-Butylbenzoate TCI M1693

Methyl 4-tert-Butylbenzoate TCI M1693

Chemical Identity

CAS No.
26537-19-9
PubChem
CID 97433·SID 87558044
Formula
C12H16O2
Molecular weight
192.25 g/mol
Purity
>98.0%(GC)
Reference databases
ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
methyl 4-tert-butylbenzoate
SMILES
CC(C)(C)C1=CC=C(C=C1)C(=O)OC
InChIKey
UPIJOAFHOIWPLT-UHFFFAOYSA-N
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Methyl 4-tert-Butylbenzoate is a chemical compound widely used in laboratory synthetic reactions. It serves as a building block in organic chemistry, providing a foundational structure for the synthesis of more complex molecules. This compound is particularly valuable in the development of aromatic compounds and their derivatives, making it an essential tool for researchers in both academic and industrial settings. Its role in organic synthesis extends to various functional group transformations, where it acts as a versatile intermediate.

The compound is known for its stability and controlled reactivity, which makes it a preferred choice in laboratory applications. Its non-polar nature allows it to dissolve in common organic solvents such as ethyl acetate and chloroform, facilitating its use in reactions like esterification and hydrolysis. These solubility characteristics enhance its utility in a wide range of chemical processes. Additionally, its relatively low toxicity ensures a safer working environment, aligning with standard laboratory safety protocols.

In Indonesian laboratories, Methyl 4-tert-Butylbenzoate is commonly utilized in organic chemistry research. It plays a key role in the synthesis of pharmaceutical compounds and other complex organic molecules. Its availability and reliability make it a standard reagent in both teaching and research laboratories. The compound’s versatility and compatibility with various reaction conditions contribute to its widespread use in chemical synthesis across different scientific disciplines.

  • Organic synthesis of aromatic compounds due to its stable molecular structure and reactivity.
  • Esterification reactions as a readily available ester functional group donor.
  • Development of pharmaceutical products as a building block for complex molecule synthesis.
  • Hydrolysis reactions because of its solubility in organic solvents and chemical stability.
  • Substitution reactions where it acts as a versatile intermediate in synthetic pathways.

Brand TCI
CAS number 26537-19-9
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Solid or liquid depending on the batch
Storage Store in a cool, dry place away from direct sunlight

Methyl 4-tert-Butylbenzoate should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air. Suitable storage containers include glass or high-density polyethylene vessels to ensure chemical stability. Due to its non-polar nature, it is important to avoid contact with incompatible substances. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment. Regular monitoring of storage conditions ensures the compound remains safe and effective for use in chemical experiments.

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