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SU0006399 SSCRPT
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SU0006399 SSCRPT
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Last modified
5/7/2020 11:32:22 AM
Creation date
9/6/2019 10:40:41 AM
Metadata
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Template:
EHD - Public
ProgramCode
2600 - Land Use Program
FileName_PostFix
SSCRPT
RECORD_ID
SU0006399
PE
2622
FACILITY_NAME
PA-0600679
STREET_NUMBER
7500
Direction
W
STREET_NAME
KILE
STREET_TYPE
RD
City
LODI
APN
00118012 13
ENTERED_DATE
1/17/2007 12:00:00 AM
SITE_LOCATION
7500 W KILE RD
RECEIVED_DATE
1/16/2007 12:00:00 AM
P_LOCATION
99
P_DISTRICT
004
QC Status
Approved
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\MIGRATIONS\K\KILE\7500\PA-0600679\SU0006399\SSC RPT.PDF
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EHD - Public
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EXTOXNET PIP -IMIDACLOPRID Page 3 of 4 <br /> • Breakdown of Chemical in Soil and Groundwater: The half-life of imidacloprid in soil is 48-190 days, <br /> depending on the amount of ground cover(it breaks down faster in soils with plant ground cover than in fallow <br /> soils) (334). Organic material aging may also affect the breakdown rate of imidacloprid. Plots treated with cow <br /> manure and allowed to age before sowing showed longer persistence of imidacloprid in soils than in plots where the <br /> manure was more recently applied, and not allowed to age (335). Imidacloprid is degraded stepwise to the primary <br /> metabolite 6-chloronicotinic acid, which eventually breaks down into carbon dioxide(336). There is generally not a <br /> high risk of groundwater contamination with imidacloprid if used as directed. The chemical is moderately soluble, <br /> and has moderate binding affinity to organic materials in soils. However, there is a potential for the compound to <br /> move through sensitive soil types including porous, gravelly, or cobbly soils, depending on irrigation practices <br /> (337). <br /> • Breakdown of Chemical in Surface Water: The half-life in water is much greater than 31 days at pH 5, 7 and 9. <br /> No other information was found. <br /> • Breakdown of Chemical in Vegetation: Imidacloprid penetrates the plant, and moves from the stem to the tips of <br /> the plant. It has been tested in a variety of application and crop types, and is metabolized following the same <br /> pathways. The most important steps were loss of the nitro group, hydroxylation at the imidazolidine ring, hydrolysis <br /> to 6-chloronicotinic acid and formation of conjugates (1). <br /> • Analytical Methods: Methods are available for determining imidacloprid residues (the 6-chloropicolyl moiety) in <br /> plant materials using HPLC with u.v. detection(338). <br /> PHYSICAL PROPERTIES AND GUIDELINES <br /> Physical Properties: <br /> • Appearance: Colorless crystals with a weak characteristic odor. <br /> • Chemical Name: 1-(6-chloro-3-pyridylmethyl)-N-nitroimidazolidin-2-ylideneamine, 1-[(6-chloro-3-pyridinyl) <br /> methyl]-N-nitro-2-imidazolidinimine. <br /> • CAS Number: 13826-41-3 <br /> • Molecular Weight: 255.7 <br /> • Water Solubility: 0.51 g/I (200 degrees C) <br /> • Solubility in Other Solvents: @ 20 degrees C: dichloromethane - 50.0 - 100.0 g/1; isopropanol- 1.0-2.0 g/1; <br /> toluene- 0.5-1.0 g/l; n-hexane - <0.1 g/1; fat- 0.061 g/100g <br /> • Melting Point: 136.4-143.8 degrees C., 143.8 degrees C (crystal form 1) 136.4 degrees C (crystal form 2) <br /> • Vapor Pressure: 0.2 uPa(20 degrees C) (1.5 X 10 to the minus 9 mmHg) <br /> • Partition Coefficient: 0.57 (22 degrees C). (1) <br /> • Adsorption Coefficient: Not Available <br /> Exposure Guidelines: <br /> • ADI: Not Available <br /> • MCL:Not Available <br /> • RID: 0.057 mg/kg/day (328) <br /> • PEL: Not Available <br /> • HA: Not Available <br /> • TLV:Not Available <br /> BASIC MANUFACTURER <br /> Bayer Agricultural Products <br /> P. O. Box 4913 <br /> Kansas City, MO 64120 <br /> http://extoxnet.orst.edu/pips/imidacio.htrn 12/20/2006 <br />
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