Piproctanyl
Last updated: 11/09/2023
(Also known as: glyphosate diammonium)
The following alerts are based on the data in the tables below. An absence of an alert does not imply the substance has no implications for human health, biodiversity or the environment but just that we do not have the data to form a judgement.
Environmental fate
Ecotoxicity
Human health
 
 
An obsolete growth inhibitor
Growth
Cereals
-
Considered obsolete but may be available in some countries
1976, first report
Not approved
Not applicable
No UK approval for use
EC Regulation 1107/2009 (repealing 91/414)
Not approved
Not applicable
Not applicable
Not applicable
No
ATAustria
BEBelgium
BGBulgaria
CYCyprus
CZCzech Republic
DEGermany
DKDenmark
EEEstonia
ELGreece
 
 
 
 
 
 
 
 
 
ESSpain
FIFinland
FRFrance
HRCroatia
HUHungary
IEIreland
ITItaly
LTLithuania
LULuxembourg
 
 
 
 
 
 
 
 
 
LVLatvia
MTMalta
NLNetherlands
PLPoland
PTPortugal
RORomania
SESweden
SISlovenia
SKSlovakia
 
 
 
 
 
 
 
 
 
ISIceland
NONorway
 
 
 
 
 
 
 
 
 
Piproctanyl is a chiral molecule. The technical material is an isomeric mixture.
C₁₈H₃₆N
CC(C)CCCC(C)CC[N+]1(CCCCC1)CC=C
No data
NTHCPJMKRGXODE-UHFFFAOYSA-N
InChI=1S/C18H36N/c1-5-13-19(14-7-6-8-15-19)16-12-18(4)11-9-10-17(2)3/h5,17-18H,1,6-16H2,2-4H3/q+1
Yes
Herbicide, Plant Growth Regulator
Quaternary ammonium compound
-
-
Synthetic
-
69309-47-3
No data found
None allocated
-
92514
No data found
266.49
rac-1-[(3R)-3,7-dimethyloctyl]-1-(prop-2-en-1-yl)piperidin-1-ium
(RS)-1-allyl-1-(3,7-dimethyloctyl)piperidinium
1-(3,7-dimethyloctyl)-1-(2-propenyl)piperidinium
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-
Not known
Not known
Not applicable
Not applicable
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-
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-
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-
-
-
-
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Soil adsorption and mobility
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Cannot be calculated
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None
Terrestrial ecotoxicology
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> 100
E2 E = Manufacturers safety data sheets 2 = Unverified data of unknown source
Low
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HUMAN HEALTH AND PROTECTION
High (class III)
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EU MRL pesticide database 
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Carcinogen
Endocrine disruptor
No data found
A0 A = Chromosome aberration (EFSA database) 0 = No data
; B0 B = DNA damage/repair (EFSA database) 0 = No data
; C0 C = Gene mutation (EFSA database) 0 = No data
; D0 D = Genome mutation (EFSA database) 0 = No data
; E0 E = Unspecified genotoxicity type (miscellaneous data source) 0 = No data
No data found
Reproduction / development effects
Acetyl cholinesterase inhibitor
Neurotoxicant
No data found
No data found
No data found
Respiratory tract irritant
Skin irritant
Skin sensitiser
No data found
No data found
No data found
Eye irritant
Phototoxicant
 
No data found
No data found
 
No information available
No information available
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Not classified: Obsolete (Not classified: Obsolete)
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piproctanyl
piproctanyl
Piproctanylium
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Record last updated:
11/09/2023
Contact:
aeru@herts.ac.uk
Please cite as:
Lewis, K.A., Tzilivakis, J., Warner, D. and Green, A. (2016) An international database for pesticide risk assessments and management. Human and Ecological Risk Assessment: An International Journal , 22 (4), 1050-1064. DOI: 10.1080/10807039.2015.1133242