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TCI

CAS 80866-75-7

3-Methyl-4-nitrobenzyl Alcohol TCI M2915

3-Methyl-4-nitrobenzyl Alcohol TCI M2915

Chemical Identity

CAS No.
80866-75-7
PubChem
CID 591360·SID 354335456
Formula
C8H9NO3
Molecular weight
167.16 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(3-methyl-4-nitrophenyl)methanol
SMILES
CC1=C(C=CC(=C1)CO)[N+](=O)[O-]
InChIKey
KOVQGYQQVNCUBR-UHFFFAOYSA-N
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3-Methyl-4-nitrobenzyl Alcohol is a chemical compound widely used as a foundational building block in laboratory synthesis. It plays a crucial role in organic chemistry by serving as a versatile intermediate in the creation of complex molecules. This compound is particularly valuable in the development of heterocyclic and non-heterocyclic structures due to its reactive functional groups. Its presence in laboratory settings is essential for a variety of chemical transformations, making it an indispensable tool for researchers working in synthetic chemistry.

The compound’s unique properties, including its polar nature and high reactivity, make it a preferred choice for many chemical reactions. The presence of both hydroxyl and nitro groups contributes to its ability to participate in multiple reaction mechanisms, such as electrophilic substitution and esterification. These characteristics allow it to interact effectively with various reagents and catalysts, enhancing its utility in both academic and industrial research environments. Its chemical stability and predictable behavior further support its reliability in laboratory applications.

In Indonesian laboratories, 3-Methyl-4-nitrobenzyl Alcohol is commonly used in organic synthesis and drug development. Its availability and consistent quality make it a trusted material for researchers aiming to produce pharmaceutical compounds and industrial chemicals. The compound’s role in supporting advanced chemical processes underscores its importance in the scientific community, particularly in the context of chemical innovation and research.

  • Synthesis of heterocyclic compounds due to its reactive functional groups and structural versatility.
  • Electrophilic substitution reactions because of its ability to interact with various reagents and catalysts.
  • Esterification processes owing to the presence of a hydroxyl group that can undergo acylation.
  • Development of pharmaceutical compounds as a key intermediate in drug molecule construction.
  • Industrial chemical production where reliable and consistent chemical building blocks are required.

Brand TCI
CAS number 80866-75-7
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard chemical supply practices
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight and incompatible materials

This compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to use sealed containers to prevent exposure to moisture and air, which could affect its stability. Due to its polar nature, it should be kept away from incompatible substances such as strong oxidizers or acids. Proper ventilation is essential when handling the material to minimize inhalation risks. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, to ensure safe handling. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use.

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