4'-Aminoacetophenone Hydrochloride

98%

  • Product Code: 67030
  CAS:    41784-08-1
Molecular Weight: 171.62 g./mol Molecular Formula: C₈H₉NOHCl
EC Number: MDL Number: MFCD00060232
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: 4'-Aminoacetophenone Hydrochloride is primarily used in organic synthesis as an intermediate for the production of various pharmaceuticals and fine chemicals. It serves as a key building block in the synthesis of compounds with potential therapeutic applications, such as anti-inflammatory and analgesic agents. Additionally, it is utilized in the development of dyes and pigments due to its aromatic amine structure, which allows for the creation of colorants with specific properties. In research, it finds application as a reagent in chemical reactions to introduce the aminoacetophenone moiety into more complex molecules. Its hydrochloride form enhances stability and solubility, making it suitable for use in aqueous reaction conditions.
Product Specification:
Test Specification
APPEARANCE White to Light yellow powder to crystal
PURITY 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days $145.11
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4'-Aminoacetophenone Hydrochloride
4'-Aminoacetophenone Hydrochloride is primarily used in organic synthesis as an intermediate for the production of various pharmaceuticals and fine chemicals. It serves as a key building block in the synthesis of compounds with potential therapeutic applications, such as anti-inflammatory and analgesic agents. Additionally, it is utilized in the development of dyes and pigments due to its aromatic amine structure, which allows for the creation of colorants with specific properties. In research, it finds application as a reagent in chemical reactions to introduce the aminoacetophenone moiety into more complex molecules. Its hydrochloride form enhances stability and solubility, making it suitable for use in aqueous reaction conditions.
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