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flamprop-methyl

Editor I.G. Ferris

 

Entity code FLAMP
CAS registry No. 52756-25-9
Family Arylalanine
Functions Herbicide
Chemical name methyl N-benzoyl-N-(3-chloro-4-fluorophenyl)-DL-alaninate (IUPAC, CAS) (EN)
Synonyms methyl (±)-N-benzoyl-N-(3-chloro-4-fluorophenyl)-2-aminopropionate
Trade names Metaven (Shell); Lancer (ICI)
Other names
Last updated 22/10/2008

Fate

Toxicology
In mammals, following oral administration, metabolism and elimination occur within 4 days.
Mammals: Acute oral LD50 for rats 1210, mice 720 mg/kg. Acute percutaneous LD50 for rats >294 mg a.i./kg (as EC formulation). Non-irritating and non-sensitizing to skin. Acute i.p. LD50 for rats 350-500 mg/kg. In 2-year feeding trials, rats receiving 2.5 mg/kg diet and dogs receiving 10 mg/kg diet showed no ill-effects.

Detection

Sampling

Methods

MRLs

Uses
Post-emergence control of wild oats (Avena spp.) in wheat (including crops undersown with clover or grass), sugar beet, and fodder beet. Also control Alopecurus myosuroides.

Notes
Flamprop-methyl is a derivative of flamprop [58667-63-3].
The name “flamprop-méthyle” is used in France.
The D-isomer of this substance has the ISO common name flamprop-M-methyl.

Bibliography
US National Library of Medicine Flamprop-methyl (http://chem.sis.nlm.nih.gov/chemidplus/ProxyServlet?objectHandle=Search&actionHandle=getAll3DMViewFiles&nextPage=jsp%2Fcommon%2FChemFull.jsp%3FcalledFrom%3Dlite&chemid=052756259&formatType=_3D)
Pestizide Flamprop-methyl III–12.3 (http://www.toxcenter.de/stoff-infos/f/flamprop-methyl.pdf)

Mode of action
Selective systemic herbicide, absorbed by the leaves. Undergoes hydrolysis to flamprop, which is translocated readily in the phloem of the leaves basipetally to the stem. Inhibits cell elongation and cell division in the stem, and hence inhibits plant growth.

Ecotoxicology
Birds: Acute oral LD50 for bobwhite quail 4640 mg/kg; pheasants, mallard ducks, domestic fowl, partridges, pigeons >1000 mg/kg.
Fish: LC50 (96 hours) for rainbow trout 4.7 mg/l.
Bees: Not toxic to bees.

Plant metabolism & residues
In plants, flamprop-methyl is hydrolyzed to the biologically-active flamprop, which then undergoes conversion to a biologically-inactive conjugate.


Physicochemical properties
Property Value
Molecular weight  0  
Melting point  0 °C  
Vapour pressure  0 mPa  
Water solubility  0 mg/l  
Octanol/water partition coefficient (log10 Kow)  0  
Dissociation constant  0  

Notes


Toxicological end points
Property Value
Rat LD50 (oral)  0 mg/kg bw  
Acceptable daily intake  0 mg/kg/day  

Notes


Environmental fate values
Property Value
Soil organic carbon partition coefficient (log10 Koc)  0 l/kg  
Soil DT50 aerobic  0 day  

Notes


Ecotoxicological end points
Property Value

Notes