Aminocyclopyrachlor

Structural formula
General
Surname	Aminocyclopyrachlor
other names	6-Amino-5-chloro-2-cyclopropyl-4-pyrimidinecarboxylic acid
Molecular formula	C 8 H 8 ClN 3 O 2
Brief description	white solid with a characteristic odor
External identifiers / databases
ECHA InfoCard	100.121.525
PubChem	17747875
Wikidata	Q4746454
properties
Molar mass	213.62 g mol −1
Physical state	firmly
Melting point	140.8 ° C
Vapor pressure	negligible
pK s value	4.63
solubility	sparingly soluble in water (3 g l −1 at 20 ° C)
safety instructions
GHS labeling of hazardous substances	no GHS pictograms
	no GHS pictograms
H and P phrases	H: 412
	P: 273
Toxicological data	> 5000 mg kg −1 ( LD 50 , rat , oral ) ; > 5000 mg kg −1 ( LD 50 , mouse / rabbit , transdermal ) ;
	As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Aminocyclopyrachlor is a chemical compound of chlorine from the group of pyrimidines .

properties

Aminocyclopyrachlor is a white crystalline solid with a characteristic odor. It is a weak acid.

use

Aminocyclopyrachlor, its potassium salt and methyl ester are used as a herbicide . It is structurally similar to aminopyralid and was developed by DuPont . It was approved in the USA in 2010. The effect is based on the influence of the auxin . The compound was assessed by EFSA in 2005. In 2011, the New York Times reported that aminocyclopyrachlor was blamed for conifer death. In the European Union and in Switzerland, aminocyclopyrachlor is not approved as a crop protection agent.

Individual evidence

↑ ^a ^b ^c ^d ^e ^f ^g ^h ⁱ ^j data sheet aminocyclopyrachlor from Sigma-Aldrich , accessed on May 22, 2017 ( PDF ).
↑ ^a ^b ^c USDA Forest Service: Aminocyclopyrachlor , Human Health and Ecological Risk Assessment - Harold Thistle, accessed August 25, 2015
↑ Entry on aminocyclopyrachlor in the Hazardous Substances Data Bank , accessed August 25, 2015.
↑ Richard P. Pohanish: Sittig's Handbook of Pesticides and Agricultural Chemicals . William Andrew, 2014, ISBN 1-4557-3157-9 , pp. 30 ( limited preview in Google Book search).
↑ EFSA: Scientific support for preparing an EU position in the 47th Session of the Codex Committee on Pesticide Residues (CCPR). In: EFSA Journal. 13, 2015, doi : 10.2903 / j.efsa.2015.4208 .
^ The New York Times: Imprelis Herbicide Suspected in Tree Deaths - The New York Times , accessed August 25, 2015
^ Directorate-General for Health and Food Safety of the European Commission: EU pesticide database ; Entry in the national directory of plant protection products in Switzerland ; Retrieved June 20, 2016.

[Sigma-1] ↑ ^a ^b ^c ^d ^e ^f ^g ^h ⁱ ^j data sheet aminocyclopyrachlor from Sigma-Aldrich , accessed on May 22, 2017 ( PDF ).

[USDA-2] USDA Forest Service: Aminocyclopyrachlor , Human Health and Ecological Risk Assessment - Harold Thistle, accessed August 25, 2015

[HSDB-3] Entry on aminocyclopyrachlor in the Hazardous Substances Data Bank , accessed August 25, 2015.

[Richard_P._Pohanish-4] Richard P. Pohanish: Sittig's Handbook of Pesticides and Agricultural Chemicals . William Andrew, 2014, ISBN 1-4557-3157-9 , pp. 30 ( limited preview in Google Book search).

[4208.pdf-5] EFSA: Scientific support for preparing an EU position in the 47th Session of the Codex Committee on Pesticide Residues (CCPR). In: EFSA Journal. 13, 2015, doi : 10.2903 / j.efsa.2015.4208 .

[The_New_York_Times-6] The New York Times: Imprelis Herbicide Suspected in Tree Deaths - The New York Times , accessed August 25, 2015

[7] Directorate-General for Health and Food Safety of the European Commission: EU pesticide database ; Entry in the national directory of plant protection products in Switzerland ; Retrieved June 20, 2016.