N,N,3,5-Tetramethylaniline, 98%
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N,N,3,5-Tetramethylaniline, 98%
N,N,3,5-Tetramethylaniline, 98%
N,N,3,5-Tetramethylaniline, 98%
Thermo Scientific Chemicals

N,N,3,5-Tetramethylaniline, 98%

CAS: 4913-13-7 | C10H15N | 149.237 g/mol
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Catalog number L09266.06
also known as L09266-06
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Quantity:
5 g
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Price (USD)
104.65
Online Exclusive
116.00
Save 11.35 (10%)
Each
Add to cart
Chemical Identifiers
CAS4913-13-7
IUPAC NameN,N,3,5-tetramethylaniline
Molecular FormulaC10H15N
InChI KeyNBFRQCOZERNGEX-UHFFFAOYSA-N
SMILESCN(C)C1=CC(C)=CC(C)=C1
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SpecificationsSpecification SheetSpecification Sheet
Assay (GC)>97.5%
Formor pale brown liquid
Refractive Index1.5420-1.5460
Appearance (Color)Clear, colourless to yellow
N,N,3,5-Tetramethylaniline was used in rapid quenching of 1,8-dihydroxyanthraquinone (DHAQ). It was also used as a catalyst in the polymeric synthesis of glycol methacrylate.

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
N,N,3,5-Tetramethylaniline was used in rapid quenching of 1,8-dihydroxyanthraquinone (DHAQ). It was also used as a catalyst in the polymeric synthesis of glycol methacrylate.

Solubility
Not miscible or difficult to mix with water.

Notes
Store in cool. Keep container tightly closed in a dry and well-ventilated place. Store away from oxidizing agent.
RUO – Research Use Only

General References:

  1. Yang Pan; Yuhe Gao; Lei Yan; Hu Pan; Jiafu Chen; Shuqin Yu. Reactivity of aromatic amines with triplet 1,8-dihydroxyanthraquinone: a laser flash photolysis study. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy,2007, 66 (1), 63-67.
  2. M Sekiguchi; K Shimai; M Moriya; R S Nowakowski. Developmental Brain Research. Developmental Brain Research.,1991, 64 (1-2), 189-195.