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CAS 928-91-6

cis-4-Hexen-1-ol TCI H0754

cis-4-Hexen-1-ol TCI H0754

Chemical Identity

Other names
cis-1-Hydroxy-4-hexene
CAS No.
928-91-6
Formula
C6H12O
Molecular weight
100.16 g/mol
Purity
>95.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(Z)-hex-4-en-1-ol
SMILES
CC=CCCCO
InChIKey
VTIODUHBZHNXFP-IHWYPQMZSA-N
MDL
MDL00148974
PubChem
CID 5365589
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TCI H0754 928-91-6 cis-4-Hexen-1-ol is a chemical compound widely used in laboratory settings for various organic synthesis reactions. As a building block in chemical reactions, it plays a crucial role in the development of complex molecular structures. This compound is part of the broader category of non-heterocyclic building blocks, making it a versatile reagent in synthetic chemistry. Its presence in laboratory workflows is essential for researchers aiming to create new compounds with specific functional groups and molecular architectures.

The compound's unique molecular structure, featuring a hydroxyl group and a double bond, contributes to its high reactivity. These characteristics make it an ideal candidate for reactions such as hydration, esterification, and addition reactions. The presence of the double bond allows for multiple reaction pathways, enhancing its utility in synthetic processes. Additionally, its distinctive aroma can serve as a visual indicator during certain chemical transformations, aiding in the monitoring of reaction progress.

In Indonesian laboratories, cis-4-Hexen-1-ol is frequently utilized in organic chemistry research across academic institutions, research centers, and industrial laboratories. Its reactivity and structural versatility make it a preferred choice for synthesizing compounds that require functional group manipulation and molecular complexity. Its applications are broad, supporting both fundamental research and applied chemical development in the region.

  • Organic synthesis is a primary application where cis-4-Hexen-1-ol is used to build complex molecules through various reaction mechanisms.
  • Esterification processes benefit from this compound’s hydroxyl group, enabling the formation of ester derivatives in controlled environments.
  • Heterogeneous catalysis applications often incorporate cis-4-Hexen-1-ol due to its reactivity and ability to participate in multiple reaction steps.
  • Flavor and fragrance development in the food and cosmetic industries relies on this compound’s aromatic properties for scent creation.
  • Polymer synthesis applications utilize cis-4-Hexen-1-ol as a monomer or functional group modifier in the production of specialty polymers.

Brand TCI
CAS number 928-91-6
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various sizes to meet laboratory and industrial needs
Physical form Liquid
Storage Store in a cool, dark place away from heat and direct sunlight

This compound should be stored in a cool, dark location, away from heat and direct sunlight to maintain its stability and prevent degradation. It is recommended to use airtight containers made of glass or high-density polyethylene to minimize exposure to moisture and air. Due to its reactivity, it should be handled in a well-ventilated area, with appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible substances like strong oxidizing agents. Ensure that storage areas are secure and inaccessible to unauthorized personnel. Regular monitoring of storage conditions is advised to maintain the compound’s integrity and ensure safe laboratory practices.

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