4-Amino-2-methyl-1-naphthol
4-Amino-2-methyl-1-naphthol is an organic compound with the molecular formula C11H11NO. It is a derivative of naphthol, a type of phenol derivative that is often used in the manufacturing of dyes and pigments. The compound is characterized by the presence of an amino group (-NH2) and a methyl group (-CH3) attached to a naphthol base.
Structure and Properties[edit | edit source]
The structure of 4-Amino-2-methyl-1-naphthol consists of a naphthol base, which is a fused two-ring system (naphthalene) with a hydroxyl group (-OH) attached. The 4-amino group is attached to the fourth carbon of the naphthalene ring, and the 2-methyl group is attached to the second carbon.
This compound exhibits typical properties of both phenols and amines. Like other phenols, it can form hydrogen bonds due to the presence of the hydroxyl group. The amino group makes it a weak base, capable of accepting a proton.
Synthesis[edit | edit source]
The synthesis of 4-Amino-2-methyl-1-naphthol can be achieved through a multi-step process. The process typically begins with the nitration of 2-methyl-1-naphthol, followed by a reduction step to introduce the amino group.
Applications[edit | edit source]
4-Amino-2-methyl-1-naphthol is primarily used in the production of dyes and pigments. Its ability to form complex structures and vibrant colors when combined with various metal ions makes it a valuable component in the dye industry.
Safety and Precautions[edit | edit source]
As with many chemical substances, handling 4-Amino-2-methyl-1-naphthol requires certain safety precautions. It is recommended to use personal protective equipment, including gloves and eye protection, when handling this compound. In case of skin or eye contact, immediate medical attention should be sought.
See Also[edit | edit source]
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Contributors: Prab R. Tumpati, MD