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Page 2 - Group 3 - Class 11-5

Group 3 Class 11-5 is led by M Dani Daroni and has 4 members: Aditya Heksa Putra, Anida Mauludina, and Yuke Djulianti. Glutaraldehyde is an organic compound with the molecular formula CH2(CH2CHO)2 that is widely used to sterilize medical equipment. It is produced industrially through the oxidation of cyclopentene or the Diels-Alder reaction of acrolein and methyl vinyl ether followed by hydrolysis. Monomeric glutaraldehyde can polymerize through aldol condensation, yielding alpha, beta-unsaturated poly-glutaraldehyde, especially under alkaline conditions.

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55 views1 page

Page 2 - Group 3 - Class 11-5

Group 3 Class 11-5 is led by M Dani Daroni and has 4 members: Aditya Heksa Putra, Anida Mauludina, and Yuke Djulianti. Glutaraldehyde is an organic compound with the molecular formula CH2(CH2CHO)2 that is widely used to sterilize medical equipment. It is produced industrially through the oxidation of cyclopentene or the Diels-Alder reaction of acrolein and methyl vinyl ether followed by hydrolysis. Monomeric glutaraldehyde can polymerize through aldol condensation, yielding alpha, beta-unsaturated poly-glutaraldehyde, especially under alkaline conditions.

Uploaded by

Yuke Djulianti
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Group 3 Class 11-5

Leader : M Dani Daroni


Members : - Aditya Heksa Putra
-

Anida Mauludina
Yuke Djulianti

Glutaraldehyde is an organic compound that belongs to the Aldehyde


functional groups. Glutaraldehyde is an organic compound with the molecular
formula CH2(CH2CHO)2. A liquid such as oil color and is widely used to sterilize
medical and dental equipment. These compounds are also used for the
processing industry-and as chemical preservatives.

Pictured above is the structural formula of glutaraldehyde


- IUPAC name : Pentane-1,5-dial
- Other names : Pentanedial, Glutardialdehyde, Glutaric acid dialdehyde, Glutaric aldehyde,
Glutaric dialdehyde, 1,5-Pentanedial
Glutaraldehyde is produced industrially by the oxidation of cyclopentene and by the
Diels-Alder reaction of acrolein and methyl vinyl ether followed by hydrolysis. Like other
dialdehydes (e.g., glyoxal), it does not exist as the dialdehyde but as the hydrate. These
hydrates adopt several structures.

Monomeric glutaraldehyde can polymerize by aldol condensation reaction yielding


alpha, beta-unsaturated poly-glutaraldehyde. This reaction usually occurs at alkaline pH
values.

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