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CAS 3556-83-0

Methyl 3-Methoxy-4-methylbenzoate TCI M1427

Methyl 3-Methoxy-4-methylbenzoate TCI M1427

Chemical Identity

CAS No.
3556-83-0
Formula
C10H12O3
Molecular weight
180.20 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
methyl 3-methoxy-4-methylbenzoate
SMILES
CC1=C(C=C(C=C1)C(=O)OC)OC
InChIKey
LLEXCSBUSVRBCA-UHFFFAOYSA-N
PubChem
CID 591123
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Methyl 3-Methoxy-4-methylbenzoate is a chemical compound widely used in organic synthesis reactions. It serves as a key building block in the development of more complex organic molecules. This compound is commonly found in chemical laboratories as a precursor for various synthetic pathways. Its versatility makes it an essential reagent for chemists working on a wide range of molecular transformations. Due to its stability and reactivity, it is frequently used in both academic and industrial research settings.

The compound's molecular structure features an ester group along with methoxy and methyl substituents, which contribute to its unique chemical properties. These characteristics enable it to participate in reactions such as esterification, hydrolysis, and substitution. Its reactivity and functional group diversity make it suitable for the synthesis of aromatic and heterocyclic compounds. Additionally, its physical properties facilitate ease of handling and purification in laboratory processes.

In Indonesian laboratories, Methyl 3-Methoxy-4-methylbenzoate is extensively used in chemical research, particularly in organic synthesis and analytical chemistry. It is a common component in experiments aimed at creating new compounds or analyzing existing ones. Many educational and research institutions rely on this compound for both teaching and experimental purposes, highlighting its importance in the chemical sciences.

  • 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 ester functional group, which readily participates in such processes.
  • In analytical chemistry, it serves as a standard for chromatographic and spectroscopic analyses due to its well-defined properties.
  • It is used in the preparation of heterocyclic compounds, which are important in pharmaceutical and agrochemical research.
  • Its stability and solubility make it suitable for use in reaction mixtures where controlled conditions are required.

Brand TCI
CAS number 3556-83-0
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per supplier specifications
Physical form Solid, crystalline appearance
Storage Store in a cool, dry place away from direct sunlight

Methyl 3-Methoxy-4-methylbenzoate should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep it in a sealed container to minimize exposure to moisture and air. Due to its chemical nature, it should be handled in a well-ventilated area to avoid inhalation of vapors. Suitable containers for storage include glass or high-density polyethylene vessels. General laboratory precautions include wearing appropriate personal protective equipment, such as gloves and safety goggles, when handling the compound. It is important to ensure that the compound is stored away from incompatible materials to maintain safety in the laboratory setting.

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