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Catalog Number:
21130
CAS Number:
14617-85-7
4-Nitrophenyl myristate
Synonym(s):
4-Nitrophenyl tetradecanoate, p-Nitrophenyl myristate, Tetradecanoic acid 4-nitrophenyl ester
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Product Information

4-Nitrophenyl myristate is a versatile ester compound widely utilized in biochemical research and pharmaceutical applications. This compound, characterized by its unique nitrophenyl group, serves as an effective substrate in enzyme assays, particularly for lipases and esterases. Its ability to mimic natural lipid substrates makes it invaluable in studying lipid metabolism and enzyme kinetics. Additionally, 4-Nitrophenyl myristate is employed in the synthesis of various bioactive molecules, enhancing its relevance in drug development and formulation.

Researchers appreciate 4-Nitrophenyl myristate for its stability and solubility in organic solvents, which facilitates its use in diverse experimental setups. Its application extends to the development of diagnostic assays and as a tool for probing membrane interactions in cellular studies. By incorporating this compound into their research, professionals can gain insights into enzymatic processes and lipid interactions, ultimately contributing to advancements in biochemistry and pharmacology.

Synonyms
4-Nitrophenyl tetradecanoate, p-Nitrophenyl myristate, Tetradecanoic acid 4-nitrophenyl ester
CAS Number
14617-85-7
Molecular Formula
C20H31NO4
Molecular Weight
349.47
MDL Number
MFCD00047731
PubChem ID
84555
Conditions
Store at 0-8°C
General Information
Synonyms
4-Nitrophenyl tetradecanoate, p-Nitrophenyl myristate, Tetradecanoic acid 4-nitrophenyl ester
CAS Number
14617-85-7
Molecular Formula
C20H31NO4
Molecular Weight
349.47
MDL Number
MFCD00047731
PubChem ID
84555
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Nitrophenyl myristate is widely utilized in research focused on

  • Enzyme Activity Studies: This compound serves as a substrate in enzyme assays, particularly for lipases, allowing researchers to study enzyme kinetics and mechanisms.
  • Drug Delivery Systems: Its properties make it suitable for formulating drug delivery systems, especially in the development of controlled-release formulations that enhance therapeutic efficacy.
  • Biochemical Research: Used in the synthesis of various biochemical probes, it aids in the investigation of cellular processes and interactions, contributing to advancements in molecular biology.
  • Cosmetic Industry: The compound is explored for its potential applications in cosmetic formulations, particularly in skin care products, due to its emollient properties.
  • Analytical Chemistry: It is employed as a standard in chromatographic techniques, helping in the accurate quantification of related compounds in complex mixtures.

Citations