Alorac
Appearance
| Names | |
|---|---|
| IUPAC name
(Z)-perchloro-4-oxopent-2-enoic acid | |
| Preferred IUPAC name
(2Z)-2,3,5,5,5-pentachloro-4-oxopent-2-enoic acid | |
Other names
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| Identifiers | |
3D model (JSmol) |
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| ChemSpider | |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C5HCl5O3 | |
| Molar mass | 286.31 g·mol−1 |
| Related compounds | |
Related compounds |
chloroacetic acid, chloropon, dalapon, flupropanate, TCA[1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Alorac is a halogenated aliphatic herbicide (plant growth regulator) which is thought to be obsolete, and released in the early 2000s, which works by inhibiting gibberellin biosynthesis.[3]
Some 18 to 27 kg of CO2 are released for every kilogram of alorac technical produced.[3]
There is little information available about alorac,[3] though it is mentioned in many lists of herbicides.[4][5][6][7][2]
References
[edit]- 1 2 "alorac data sheet". www.bcpcpesticidecompendium.org. BCPC.
- 1 2 MacBean, C. (2012). A World Compendium The Pesticide Manual Sixteenth Edition. BCPC. ISBN 978 1 901396 86 7.
- 1 2 3 4 Hertfordshire, University of. "Alorac". sitem.herts.ac.uk. Retrieved 12 April 2026.
- ↑ "Pesticide List". www.lilab-ecust.cn. Pesticide Target Interaction Database.
- ↑ Panayi, Aristos; Sayer, Chad Richard Ord; Wells, Andrew John (16 October 2008). "PATENT: Herbicide Composition".
- ↑ Bovey, R. W.; Meyer, R. E.; Morton, H.L. (May 1979). "The Use of a Woody Plant Nursery in Herbicide Research" (PDF). Tho Texas Agricultural Experiment Station.
- ↑ "Acceptable Common Names and Chemical Names for the Ingredient Statement on Pesticide Labels: Fourth Edition". EPA. National Service Center for Environmental Publications (NSCEP). 1979.
External links
[edit]- Alorac in the Pesticide Properties DataBase (PPDB)
