Difference between revisions of "Glutaraldehyde"
Jump to navigation
Jump to search
(3 intermediate revisions by 2 users not shown) | |||
Line 2: | Line 2: | ||
A strong smelling gas sold commercially as a 25% aqueous solution. Glutaraldehyde polymerizes in water to form a clear viscous liquid. It is used as a biocide which acts by disrupting the cells of [[lichen]], [[mold (fungus)|mold]], bacteria, and [[fungus|fungi]] by alkylating and crosslinking the [[protein|proteins]]. Glutaraldehyde is also used as a synthetic tanning agent for [[leather|leathers]]. | A strong smelling gas sold commercially as a 25% aqueous solution. Glutaraldehyde polymerizes in water to form a clear viscous liquid. It is used as a biocide which acts by disrupting the cells of [[lichen]], [[mold (fungus)|mold]], bacteria, and [[fungus|fungi]] by alkylating and crosslinking the [[protein|proteins]]. Glutaraldehyde is also used as a synthetic tanning agent for [[leather|leathers]]. | ||
− | + | [[[SliderGallery rightalign|glutaraldehyde.jpg~Chemical structure]]] | |
== Synonyms and Related Terms == | == Synonyms and Related Terms == | ||
glutaric dialdehyde; 1,5-pentanedial; glutaral; 1,3-diformylpropane; Cidex; Glutarol; Novaruca; Verucasep; Ucaricide | glutaric dialdehyde; 1,5-pentanedial; glutaral; 1,3-diformylpropane; Cidex; Glutarol; Novaruca; Verucasep; Ucaricide | ||
− | + | == Risks == | |
− | == | + | * Toxic by inhalation and ingestion. |
+ | * Skin contact causes irritation. | ||
+ | *Fisher Scientific: [https://fscimage.fishersci.com/msds/10421.htm MSDS] | ||
+ | == Physical and Chemical Properties == | ||
Soluble in water. | Soluble in water. | ||
Line 22: | Line 25: | ||
|- | |- | ||
! scope="row"| Melting Point | ! scope="row"| Melting Point | ||
− | | -14 | + | | -14 C |
|- | |- | ||
! scope="row"| Density | ! scope="row"| Density | ||
− | | 0.7 | + | | 0.7 g/ml |
|- | |- | ||
! scope="row"| Molecular Weight | ! scope="row"| Molecular Weight | ||
Line 34: | Line 37: | ||
|- | |- | ||
! scope="row"| Boiling Point | ! scope="row"| Boiling Point | ||
− | | 187-189 (dec) | + | | 187-189 C (dec) |
|} | |} | ||
− | == | + | == Resources and Citations== |
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
* Richard S. Lewis, ''Hawley's Condensed Chemical Dictionary'', Van Nostrand Reinhold, New York, 10th ed., 1993 | * Richard S. Lewis, ''Hawley's Condensed Chemical Dictionary'', Van Nostrand Reinhold, New York, 10th ed., 1993 | ||
Line 49: | Line 46: | ||
* ''The Merck Index'', Martha Windholz (ed.), Merck Research Labs, Rahway NJ, 10th edition, 1983 Comment: entry 4480 | * ''The Merck Index'', Martha Windholz (ed.), Merck Research Labs, Rahway NJ, 10th edition, 1983 Comment: entry 4480 | ||
− | * Wikipedia | + | * Wikipedia: http://en.wikipedia.org/wiki/Glutaraldehyde (Accessed Mar. 1, 2006) |
[[Category:Materials database]] | [[Category:Materials database]] |
Latest revision as of 07:49, 30 August 2022
Description
A strong smelling gas sold commercially as a 25% aqueous solution. Glutaraldehyde polymerizes in water to form a clear viscous liquid. It is used as a biocide which acts by disrupting the cells of Lichen, mold, bacteria, and fungi by alkylating and crosslinking the proteins. Glutaraldehyde is also used as a synthetic tanning agent for leathers.
Synonyms and Related Terms
glutaric dialdehyde; 1,5-pentanedial; glutaral; 1,3-diformylpropane; Cidex; Glutarol; Novaruca; Verucasep; Ucaricide
Risks
- Toxic by inhalation and ingestion.
- Skin contact causes irritation.
- Fisher Scientific: MSDS
Physical and Chemical Properties
Soluble in water.
Composition | OHC(CH2)3CHO |
---|---|
CAS | 111-30-8 |
Melting Point | -14 C |
Density | 0.7 g/ml |
Molecular Weight | mol. wt. = 100.12 |
Refractive Index | 1.4338 |
Boiling Point | 187-189 C (dec) |
Resources and Citations
- Richard S. Lewis, Hawley's Condensed Chemical Dictionary, Van Nostrand Reinhold, New York, 10th ed., 1993
- The Merck Index, Martha Windholz (ed.), Merck Research Labs, Rahway NJ, 10th edition, 1983 Comment: entry 4480
- Wikipedia: http://en.wikipedia.org/wiki/Glutaraldehyde (Accessed Mar. 1, 2006)