Xylyl carb

Structural formula
General
Surname	Xylyl carb
other names	3,4-xylyl methyl carbamate; MPMC;
Molecular formula	C 10 H 13 NO 2
External identifiers / databases
EC number	219-364-9
ECHA InfoCard	100.017.605
PubChem	17040
Wikidata	Q2598558
properties
Molar mass	179.22 g mol −1
Physical state	firmly
Melting point	79.5 ° C
solubility	in water: 580 mg l −1 at 20 ° C
safety instructions
H and P phrases	H: 302-410
	P: ?
Toxicological data	290 mg kg −1 ( LD 50 , rat , oral ) ; 1000 mg kg −1 ( LD 50 , rat , transdermal ) ;
	As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Xylylcarb is a chemical compound from the group of carbamates .

Extraction and presentation

Xylyl carb can be obtained by reacting 3,4-xylenol with methyl isocyanate or alternatively with phosgene and methylamine .

properties

Xylyl carb is a solid. It hydrolyzes under alkaline conditions.

use

Xylylcarb is used as an insecticide . It is mainly used to control cicadas and other biting insects on rice and fruits. The effect is based on the inhibition of cholinesterase .

Admission

In the states of the European Union and thus in Germany, Austria and Switzerland, no pesticides with this active ingredient are permitted.

Individual evidence

↑ ^a ^b S. D. Gangolli: The Dictionary of Substances and their Effects (DOSE): TZ and Index . Royal Society of Chemistry, 1999, ISBN 0-85404-838-3 , pp. 661 ( limited preview in Google Book search).
↑ ^a ^b ^c Terry R. Roberts, David H. Hutson, Philip W. Lee, Peter H. Nicholls: Metabolic Pathways of Agrochemicals: Part 2: Insecticides and Fungicides . Royal Society of Chemistry, 1999, ISBN 0-85404-499-X , pp. 75 ( limited preview in Google Book search).
↑ ^a ^b ^c ^d Entry for CAS no. 2425-10-7 in the GESTIS substance database of the IFA , accessed on September 18, 2012(JavaScript required) .
↑ Entry on 3,4-xylyl methylcarbamate in the Classification and Labeling Inventory of the European Chemicals Agency (ECHA), accessed on August 1, 2016. Manufacturers or distributors can expand the harmonized classification and labeling .
↑ Thomas A. Unger: Pesticide Synthesis Handbook . William Andrew, 1996, ISBN 0-8155-1401-8 , pp. 98 ( limited preview in Google Book search).
^ Directorate-General for Health and Food Safety of the European Commission: EU pesticide database ; Entry in the national registers of plant protection products in Switzerland , Austria and Germany ; accessed on March 12, 2016.

[S._D._Gangolli-1] S. D. Gangolli: The Dictionary of Substances and their Effects (DOSE): TZ and Index . Royal Society of Chemistry, 1999, ISBN 0-85404-838-3 , pp. 661 ( limited preview in Google Book search).

[Terry_R._Roberts,_David_H._Hutson,_Philip_W._Lee,_Peter_H._Nicholls-2] Terry R. Roberts, David H. Hutson, Philip W. Lee, Peter H. Nicholls: Metabolic Pathways of Agrochemicals: Part 2: Insecticides and Fungicides . Royal Society of Chemistry, 1999, ISBN 0-85404-499-X , pp. 75 ( limited preview in Google Book search).

[GESTIS-3] Entry for CAS no. 2425-10-7 in the GESTIS substance database of the IFA , accessed on September 18, 2012(JavaScript required) .

[CLP_100.017.605-4] Entry on 3,4-xylyl methylcarbamate in the Classification and Labeling Inventory of the European Chemicals Agency (ECHA), accessed on August 1, 2016. Manufacturers or distributors can expand the harmonized classification and labeling .

[Thomas_A._Unger-5] Thomas A. Unger: Pesticide Synthesis Handbook . William Andrew, 1996, ISBN 0-8155-1401-8 , pp. 98 ( limited preview in Google Book search).

[PSM-6] Directorate-General for Health and Food Safety of the European Commission: EU pesticide database ; Entry in the national registers of plant protection products in Switzerland , Austria and Germany ; accessed on March 12, 2016.