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CAS 104-62-1

2-Phenylethyl Formate TCI F0363

2-Phenylethyl Formate TCI F0363

Chemical Identity

Other names
Formic Acid Phenethyl Ester · Phenethyl Formate · Formic Acid 2-Phenylethyl Ester
CAS No.
104-62-1
PubChem
CID 7711·SID 87570134
Formula
C9H10O2
Molecular weight
150.18 g/mol
Purity
>95.0%(GC)
Reference databases
ChEBI·ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-phenylethyl formate
SMILES
C1=CC=C(C=C1)CCOC=O
InChIKey
IKDIJXDZEYHZSD-UHFFFAOYSA-N
MDL
MDL00021046
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2-Phenylethyl Formate is a chemical compound widely used in organic synthesis reactions, particularly in the formation of aromatic compounds and esters. It serves as a crucial building block in laboratories, enabling the construction of complex molecular structures. This versatile reagent is essential for chemists working on a variety of synthetic pathways due to its ability to participate in esterification and hydrolysis reactions. Its stability and controlled reactivity make it a reliable choice for experimental work.

The compound’s molecular structure, consisting of a phenyl group and an ethyl group, contributes to its favorable reactivity in various chemical processes. Its stability under normal laboratory conditions ensures consistent performance in experiments. Additionally, its distinct aroma makes it suitable for applications in the fragrance and flavor industries. The compound’s resistance to degradation allows it to be stored for extended periods without losing its chemical activity.

In Indonesian laboratories, 2-Phenylethyl Formate is commonly used in pure chemical research, pharmaceutical development, and quality testing of raw materials. Its availability and reliability make it a preferred choice for both academic and industrial applications. The compound’s role in creating functional molecules supports its use in diverse scientific fields, including drug discovery and material science.

  • Organic synthesis reactions benefit from 2-Phenylethyl Formate due to its reactivity in esterification and hydrolysis processes.
  • Pharmaceutical development utilizes this compound to create aromatic and ester-based compounds essential for drug formulations.
  • Flavor and fragrance industry applications rely on its distinct aroma for the creation of synthetic aroma compounds.
  • Quality control testing in chemical laboratories uses it as a standard reference for assessing purity and reactivity of similar compounds.
  • Research in material science employs it for the synthesis of complex organic molecules with specific functional groups.

Brand TCI
CAS number 104-62-1
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight

2-Phenylethyl Formate should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to keep the compound in a tightly sealed container to prevent evaporation and contamination. Due to its chemical nature, it should be handled in a well-ventilated area to avoid inhalation of vapors. Proper personal protective equipment, such as gloves and safety goggles, should be worn when handling the compound. Avoid contact with skin and eyes, and ensure that spillage is cleaned up promptly with appropriate safety measures. The compound is non-hazardous under normal storage conditions but should be treated with care in accordance with standard laboratory safety protocols.

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