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HS Code |
143849 |
| Product Name | 2-Aminoacetophenone Hydrochloride |
| Cas Number | 2140-72-3 |
| Molecular Formula | C8H10ClNO |
| Molecular Weight | 171.62 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 141-145°C |
| Solubility | Soluble in water |
| Purity | Typically ≥98% |
| Synonyms | o-Aminoacetophenone hydrochloride |
| Smiles | CC(=O)C1=CC=CC=C1N.Cl |
As an accredited 2-Aminoacetophenone Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Aminoacetophenone Hydrochloride is supplied in a 25g amber glass bottle with a secure screw cap and clear hazard labeling. |
| Shipping | 2-Aminoacetophenone Hydrochloride is shipped in tightly sealed containers, protected from moisture and light. It is typically transported as a non-hazardous, solid substance under ambient temperature. Packaging meets safety and regulatory standards, ensuring secure handling and minimal exposure during transit. Proper labeling and documentation accompany each shipment for compliance and traceability. |
| Storage | 2-Aminoacetophenone Hydrochloride should be stored in a tightly sealed container, away from moisture and direct sunlight. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature (15–25°C). Avoid sources of ignition and incompatible substances, such as strong oxidizers. Label storage clearly and ensure only authorized, trained personnel have access. |
Applications of 2-Aminoacetophenone Hydrochloride in Industrial Manufacturing2-Aminoacetophenone hydrochloride plays an essential role as a specialty chemical intermediate in several advanced manufacturing sectors. Its unique properties as a crystalline hydrochloride salt make it suitable for a variety of downstream transformations, particularly in pharmaceutical, agrochemical, and high-grade fragrance synthesis. Below, we detail the primary industrial application areas with operational guidance, compliance requirements, and final products derived from active industry partnerships and production experience. 1. Pharmaceutical API Synthesis: Anilide-Based Drug IntermediatesProducers of analgesic, anti-inflammatory, and antimicrobial drugs use 2-aminoacetophenone hydrochloride as a key intermediate in anilide-based synthesis. This compound supports amide coupling, reductive amination, and heterocycle formation steps for complex API molecules. Manufacturers control process conditions tightly to ensure residual salt handling and consistent lot-to-lot quality. The conversion routes align with cGMP protocols and require robust impurity profile management to meet global pharmacopeia submissions. Industry compliance standards
Typical usage ratio
Downstream process integration
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2. Agrochemical Active Ingredient ProductionLeading agricultural chemical manufacturers apply 2-aminoacetophenone hydrochloride in the synthesis of selective herbicides and insect growth regulators. The amine functionality enables rapid coupling with carboxylic acids or activated chlorides, supporting production of nitrogen-containing agroactive ingredients. Regulatory oversight covers purity, traceability, and process water discharge regarding hydrochloride management. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Fine Fragrance and Aroma Ingredient SynthesisThe specialty fragrance industry employs 2-aminoacetophenone hydrochloride for creating perfume-grade keynotes and tobacco flavorants, especially in synthesis pathways for methyl anthranilate or orient-influenced aldehydic components. Manufacturers tightly monitor purity and residual hydrochloride content, as downstream olfactory compound routes require well-controlled starting materials to achieve target scent profiles and regulatory food-grade limits. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Dye and Pigment Intermediate ManufacturingColorant and pigment manufacturers adopt 2-aminoacetophenone hydrochloride for the formation of azo dye intermediates and as a key building block in anthraquinone pigment synthesis. The amine group’s reactivity supports diazotization reactions, allowing precise shade control in final dye output. Strictly controlled process streams avoid contamination by chloride ions, and quality teams implement rigorous downstream purification. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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