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Hunig's Base

The Whyte Group of Companies. Auxiliary reagent in organic synthesis. Replaces Triethylamine and Dimethyl Aniline. Some types of reaction requiring an auxiliary base. Recovery and recycle of N,N-Diisopropylethylamine is relatively straightforward because of its low solubility in water. N,N-Diisopropylethylamine can be simply extracted from water-immiscible organic reaction media, as its salt, in the aqueous phase. Send mail to info@hunigs.com. With questions or comments about this web site.

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Hunig's Base | whytechemicalsfrance.com Reviews
<META>
DESCRIPTION
The Whyte Group of Companies. Auxiliary reagent in organic synthesis. Replaces Triethylamine and Dimethyl Aniline. Some types of reaction requiring an auxiliary base. Recovery and recycle of N,N-Diisopropylethylamine is relatively straightforward because of its low solubility in water. N,N-Diisopropylethylamine can be simply extracted from water-immiscible organic reaction media, as its salt, in the aqueous phase. Send mail to info@hunigs.com. With questions or comments about this web site.
<META>
KEYWORDS
1 page up
2 n n diisopropylethylamine
3 proton acceptor/scavenger
4 low nucleophilicity
5 low self alkylation
6 low water solubility
7 recyclable
8 increases process efficiency
9 reduces process costs
10 peptide synthesis
CONTENT
Page content here
KEYWORDS ON
PAGE
page up,n n diisopropylethylamine,proton acceptor/scavenger,low nucleophilicity,low self alkylation,low water solubility,recyclable,increases process efficiency,reduces process costs,peptide synthesis,recovery and recycle
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Hunig's Base | whytechemicalsfrance.com Reviews

https://whytechemicalsfrance.com

The Whyte Group of Companies. Auxiliary reagent in organic synthesis. Replaces Triethylamine and Dimethyl Aniline. Some types of reaction requiring an auxiliary base. Recovery and recycle of N,N-Diisopropylethylamine is relatively straightforward because of its low solubility in water. N,N-Diisopropylethylamine can be simply extracted from water-immiscible organic reaction media, as its salt, in the aqueous phase. Send mail to info@hunigs.com. With questions or comments about this web site.

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Hunigs Feedback Page

http://www.whytechemicalsfrance.com/feedback.htm

The Whyte Group of Companies. Please tell us what you think about our web site, company, products, or services. If you provide us with your contact information, we will be able to reach you in case we have any questions. FrontPage Save Results Component]. Send mail to info@hunigs.com. With questions or comments about this web site. Last modified: May 17, 2001.

2

Hunig's Base

http://www.whytechemicalsfrance.com/index.htm

The Whyte Group of Companies. Auxiliary reagent in organic synthesis. Replaces Triethylamine and Dimethyl Aniline. Some types of reaction requiring an auxiliary base. Recovery and recycle of N,N-Diisopropylethylamine is relatively straightforward because of its low solubility in water. N,N-Diisopropylethylamine can be simply extracted from water-immiscible organic reaction media, as its salt, in the aqueous phase. Send mail to info@hunigs.com. With questions or comments about this web site.

3

Hunigs Table of Contents Page

http://www.whytechemicalsfrance.com/toc.htm

The Whyte Group of Companies. This site Details some of the products available from the Fine Chemicals Division of Whyte Chemicals and in particular Hunig's Base. For information on other products supplied by Whyte Chemicals Ltd please click here. N N Dimethyl Ethylene Diamine. N N N' N-Tetramethylethylene Diamine. N N-Disubstituted Ethylene Diamines. Hunigs Table of Contents Page. Send mail to info@hunigs.com. With questions or comments about this web site. Last modified: May 17, 2001.

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Hunig's Base

The Whyte Group of Companies. Auxiliary reagent in organic synthesis. Replaces Triethylamine and Dimethyl Aniline. Some types of reaction requiring an auxiliary base. Recovery and recycle of N,N-Diisopropylethylamine is relatively straightforward because of its low solubility in water. N,N-Diisopropylethylamine can be simply extracted from water-immiscible organic reaction media, as its salt, in the aqueous phase. Send mail to info@hunigs.com. With questions or comments about this web site.

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Hunig's Base

The Whyte Group of Companies. Auxiliary reagent in organic synthesis. Replaces Triethylamine and Dimethyl Aniline. Some types of reaction requiring an auxiliary base. Recovery and recycle of N,N-Diisopropylethylamine is relatively straightforward because of its low solubility in water. N,N-Diisopropylethylamine can be simply extracted from water-immiscible organic reaction media, as its salt, in the aqueous phase. Send mail to info@hunigs.com. With questions or comments about this web site.

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Hunig's Base

The Whyte Group of Companies. Auxiliary reagent in organic synthesis. Replaces Triethylamine and Dimethyl Aniline. Some types of reaction requiring an auxiliary base. Recovery and recycle of N,N-Diisopropylethylamine is relatively straightforward because of its low solubility in water. N,N-Diisopropylethylamine can be simply extracted from water-immiscible organic reaction media, as its salt, in the aqueous phase. Send mail to info@hunigs.com. With questions or comments about this web site.

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Hunig's Base

The Whyte Group of Companies. Auxiliary reagent in organic synthesis. Replaces Triethylamine and Dimethyl Aniline. Some types of reaction requiring an auxiliary base. Recovery and recycle of N,N-Diisopropylethylamine is relatively straightforward because of its low solubility in water. N,N-Diisopropylethylamine can be simply extracted from water-immiscible organic reaction media, as its salt, in the aqueous phase. Send mail to info@hunigs.com. With questions or comments about this web site.

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