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Acetanilide
[CAS# 103-84-4]

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Complete supplier list of Acetanilide
Identification
Classification Organic raw materials >> Amino compound >> Cycloalkylamines, aromatic monoamines, aromatic polyamines and derivatives and salts
Name Acetanilide
Synonyms N-Phenylacetamide
Molecular Structure CAS # 103-84-4, Acetanilide, N-Phenylacetamide
Molecular Formula C8H9NO
Molecular Weight 135.16
CAS Registry Number 103-84-4
EC Number 203-150-7
SMILES CC(=O)NC1=CC=CC=C1
Properties
Density 1.121 g/mL (Expl.)
Melting point 113-115 ºC (Expl.)
Boiling point 304 ºC (Expl.)
Flash point 161 ºC *Expl.)
Water solubility 5 g/L (25 ºC)
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H302    Details
Precautionary Statements P264-P270-P301+P317-P330-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H302
Specific target organ toxicity - repeated exposureSTOT RE1H372
Reproductive toxicityRepr.2H361d
Eye irritationEye Irrit.2H319
Skin irritationSkin Irrit.2H315
Specific target organ toxicity - single exposureSTOT SE3H335
Acute toxicityAcute Tox.4H312
Specific target organ toxicity - single exposureSTOT SE1H370
Reproductive toxicityRepr.2H361
Acute toxicityAcute Tox.4H332
Specific target organ toxicity - single exposureSTOT SE3H336
SDS Available
up Discovory and Applicatios
Acetanilide is an organic compound that belongs to the class of acylated anilines. It was first synthesized in the mid-19th century and became one of the earliest analgesic and antipyretic drugs used in medicine. Its molecular structure consists of an aniline group with an acetyl functional group, which enhances its stability and modifies its biological activity. The discovery of acetanilide marked a significant advancement in pharmaceutical chemistry and paved the way for the development of safer and more effective drugs.

Acetanilide was first introduced as a medicinal compound in the 1880s when it was found to possess fever-reducing and pain-relieving properties. Initially marketed under various trade names, it gained popularity as a treatment for fever and headaches. However, prolonged use revealed its toxic effects, including methemoglobinemia, a condition in which oxygen transport in the blood is impaired. These adverse effects led to the eventual replacement of acetanilide with its safer derivatives, such as paracetamol (acetaminophen), which remains a widely used analgesic and antipyretic today.

Despite its decline in pharmaceutical applications, acetanilide continues to be utilized in various industrial and chemical processes. It serves as a precursor in the synthesis of dyes, rubber accelerators, and stabilizers for cellulose esters. Its role in the production of azo dyes is particularly significant, as it provides the structural framework for many colorants used in textiles, plastics, and printing inks. The compound's ability to enhance the thermal stability of rubber has also made it an important additive in the manufacturing of vulcanized rubber products.

In the field of agriculture, acetanilide derivatives have been developed as herbicides, particularly in the control of weed growth in crops such as corn and soybeans. These derivatives exhibit selective action against undesirable plant species while minimizing harm to the cultivated crops. The herbicidal properties of acetanilide-based compounds have been extensively studied, leading to the development of improved formulations with enhanced efficacy and reduced environmental impact.

Acetanilide has also played a role in academic and industrial research. It is frequently used as a model compound in organic chemistry laboratories for studying amide functional groups and their reactions. Its reactivity and structural properties make it a valuable reference substance for experiments involving acetylation, hydrolysis, and reduction reactions.

Environmental and safety concerns regarding acetanilide and its derivatives have led to stringent regulations on their use. While acetanilide itself is no longer employed as a drug, its industrial applications continue under controlled conditions to ensure minimal exposure and environmental contamination. Researchers continue to explore alternative compounds that retain the beneficial properties of acetanilide while mitigating its toxic effects.

The legacy of acetanilide in pharmaceutical and industrial chemistry remains significant. Its discovery and widespread use in the late 19th and early 20th centuries contributed to the advancement of medicinal chemistry and the development of safer analgesic compounds. Although its direct medical applications have ceased, its role in chemical synthesis, materials science, and agricultural chemistry ensures its continued relevance in various scientific and industrial fields.
Market Analysis Reports
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