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Catalog Number:
42480
4-(Dimethylamino)benzaldehyde
Purity:
≥ 99% (HPLC)
Synonym(s):
Ehrlich's reagent
Documents
$42.46 /25G
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Product Information

4-(Dimethylamino)benzaldehyde, also known as p-Dimethylaminobenzaldehyde, is a versatile organic compound widely utilized in various industries, particularly in the synthesis of dyes and pharmaceuticals. This compound features a dimethylamino group that enhances its reactivity, making it an essential intermediate in the production of azo dyes, which are known for their vibrant colors and stability. Additionally, it serves as a key reagent in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals, due to its ability to undergo electrophilic aromatic substitution reactions.

Researchers and industry professionals appreciate 4-(Dimethylamino)benzaldehyde for its unique properties, such as its strong UV absorption and fluorescence characteristics, which make it valuable in analytical chemistry applications, including spectrophotometry. Its role in the development of colorimetric assays and as a reagent in the detection of aldehydes further underscores its importance. With its broad range of applications, this compound is a reliable choice for those seeking efficiency and effectiveness in their chemical processes.

Synonyms
Ehrlich's reagent
Purity
≥ 99% (HPLC)
Molecular Formula
C9H11NO
MDL Number
MFCD00003381
PubChem ID
7479
Melting Point
72 - 75 °C
Boiling Point
176 - 177 °C
Conditions
Store at RT
General Information
Synonyms
Ehrlich's reagent
Purity
≥ 99% (HPLC)
Molecular Formula
C9H11NO
MDL Number
MFCD00003381
PubChem ID
7479
Melting Point
72 - 75 °C
Boiling Point
176 - 177 °C
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-(Dimethylamino)benzaldehyde is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various organic molecules, including dyes and pharmaceuticals, due to its reactive aldehyde group.
  • Fluorescent Dyes: It is commonly used in the production of fluorescent dyes, which are essential in biological imaging and labeling applications, enhancing visibility in microscopy.
  • Pharmaceutical Development: The compound is important in the development of certain pharmaceuticals, particularly those targeting neurological disorders, due to its ability to cross the blood-brain barrier.
  • Analytical Chemistry: It is utilized in analytical techniques such as chromatography and spectroscopy, where it acts as a derivatizing agent to improve detection limits and resolution.
  • Polymer Chemistry: In the field of polymer science, it is used to modify polymers for specific properties, such as increased solubility or enhanced optical characteristics.

Citations