1982-49-6 Usage
Description
SIDURON is a pre-emergence and post-emergence phenylurea herbicide, primarily used for the control of annual grass weeds. It functions by inhibiting photosynthesis and is characterized as a colorless or white crystalline solid or powder that is odorless. The commercial product is available as an emulsifiable concentrate.
Uses
Used in Agricultural Industry:
SIDURON is used as a selective pre-emergence herbicide for controlling annual weed grasses, such as crabgrass, foxtail, and barnyard grass. It is applied to newly seeded or established turf and lawn grasses, as well as a pre-emergence treatment to bare soil following spring seeding. It is registered for use in the U.S. but not listed for use in EU countries.
Trade name
GREENFIELD?; GRO-TONE?[C]; H-1318?; TREY?; TUPERSAN?
Potential Exposure
A phenyl urea preemergence herbicide
used to control annual grasses (e. g., crabgrass, foxtail, and
barnyard grass) and on newly seeded or established turf
and lawn grasses and as bare soil treatment following
spring seeding.
Environmental Fate
Soil. A fungus and two Pseudomonas spp. isolated from soil degraded siduron to form
the major metabolites: 1-(4-hydroxy-2-methylcyclohexyl)-3-(p-hydroxyphenyl)urea, 1-(4-
hydroxy-2-methylcyclohexyl)-3-phenylurea and 1-(4-hydroxyphenyl)-3-(2-methycyclohexyl)urea (Belasco and Langsdorf, 1969).
Plant. After 8 days following absorption in barley plants, no metabolites were detected
(Splittstoesser and Hopen, 1968).
Shipping
UN2767 Phenyl urea pesticides, solid, toxic,
Hazard Class: 6.1; Labels: 6.1-Poisonous materials.
UN3002 Phenyl urea pesticides, liquid, toxic, Hazard
Class: 6.1; Labels: 6.1-Poisonous materials.
Waste Disposal
Incinerate in a unit with efflu-
ent gas scrubbing. Containers must be disposed of properly
by following package label directions or by contacting your
local or federal environmental control agency, or by
contacting your regional EPA office.
Check Digit Verification of cas no
The CAS Registry Mumber 1982-49-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,8 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1982-49:
(6*1)+(5*9)+(4*8)+(3*2)+(2*4)+(1*9)=106
106 % 10 = 6
So 1982-49-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H11F3N2O/c1-15(2)9(16)14-8-5-3-4-7(6-8)10(11,12)13/h3-6H,1-2H3,(H,14,16)
1982-49-6Relevant articles and documents
A novel synthesis of isocyanates and ureas via β-elimination of haloform
Braverman,Cherkinsky,Kedrova,Reiselman
, p. 3235 - 3238 (2007/10/03)
A novel synthesis of isocyanates via base-induced β-elimination of haloform from N-monosubstituted trihaloacetamides is described. The rate of reaction exhibits a strong dependence on the nature of the trihalomethyl group. Thus, while the reaction of tribromoacetamides proceeds at room temperature and the reaction of trichloroacetamides requires heating in polar solvents, no reaction could be observed for any of the corresponding trifluoro derivatives. This novel β-elimination of haloform from stable and readily available trihaloacetamides was applied to a 'one-pot' synthesis of ureas which avoids the use of phosgene and isolation of isocyanates.
Process of improving activity of herbicides and fertilizers using N-(2-hydroxyethyl)-acetamide or -propanamide
-
, (2008/06/13)
The invention is related to the use of certain water-soluble compounds known as such and having the Formula for the modulation of membrane dependent metabolism processes within living cells, in particular with relation to transport phenomena and cell procedures which are induced or influenced by active agents supplied from outside the cell, products containing these substances for the above described uses and processes using these products.
HYPOGLYCAEMIC AGENTS.
HAYMAN,PETROW,STEPHENSON
, p. 538 - 548 (2007/10/07)
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