4-Dimethylaminobenzoyl chloride, 97%
Thermo Scientific Chemicals

4-Dimethylaminobenzoyl chloride, 97%

CAS: 4755-50-4 | C9H10ClNO | 183.635 g/mol
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5 g
25 g
Catalog number L14176.06
also known as L14176-06
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Quantity:
5 g
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Price (USD)
45.65
Special offer
Online exclusive
Ends: 28-Dec-2026
53.40
Save 7.75
Each
Chemical Identifiers
CAS4755-50-4
IUPAC Name4-(ethylamino)benzoyl chloride
Molecular FormulaC9H10ClNO
InChI KeyXFLQAKBFRUFBJS-UHFFFAOYSA-N
SMILESCCNC1=CC=C(C=C1)C(Cl)=O
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to cream to yellow to brown
FormCrystals or powder or crystalline powder or lumps
Assay (Titration ex Chloride)≥96.0 to ≤104.0%
4-Dimethylaminobenzoyl chloride is used to make other chemicals. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals and agrochemicals.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
4-Dimethylaminobenzoyl chloride is used to make other chemicals. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals and agrochemicals.

Solubility
Reacts with water.

Notes
It is sensitive to moisture. Handle and store under an inert atmosphere. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Containers which are opened must be carefully resealed and kept upright to prevent leakage. Air and moisture sensitive.
RUO – Research Use Only

General References:

  1. Bing Ma.; Kurt D. Hankenson.; James E. Dennis, Arnold I. Caplan.; Steven A. Goldstein.; Michael R. Kilbourn. A simple method for stem cell labeling with fluorine 18. Nuclear Medicine and Biology. 2005, 32 (7), 701-705.
  2. Yu Chen.; Johan Loccufier.; Luc Vanmaele.; Emilie Barriau.; Holger Frey. Novel Multifunctional Polymeric Photoinitiators and Photo-Coinitiators Derived from Hyperbranched Polyglycerol. Macromolecular Chemistry and Physics. 2007, 208 (15), 1694-1706.