1610-18-0 Usage
Chemical Properties
Colorless crystalline solid or white powder.
Odorless.
Uses
Different sources of media describe the Uses of 1610-18-0 differently. You can refer to the following data:
1. Nonselective herbicide.
2. Nonselective preemergence and postemergence herbicide used to control most
annual and perennial broad-leaved weeds, grasses and brush weeds on noncrop land.
Definition
ChEBI: A methoxy-1,3,5-triazine that is 6-methoxy-1,3,5-triazine-2,4-diamine in which the one of the hydrogens of each amino group is substituted by an isopropyl group.
Hazard
Toxic by ingestion.
Agricultural Uses
Herbicide: A non-selective pre-emergence and post-emergence herbicide. Use around buildings, storage areas, industrial sites, fences, recreational areas, rights-of-way, railroads, pipelines, lumberyards, tank farms, and similar areas. Controls broadleaf weeds and grasses over an extended period of time. Not listed for use in EU countries. Registered for use in the U.S.
Trade name
ACME? Prometon; G-31435?; GESAFRAM? 50; GESAFRAM?; GESAGRAM?; GROUND ZERO?; KLEENWALK?; NIX?; NOXALL?; ONTRACK?; PRIMATOL? (prometon); PROMETONE?; WEED-GO?
Potential Exposure
A nonselective pre-emergence and
postemergence triazine herbicide. Use around buildings,
storage areas, industrial sites, fences, recreational areas,
rights-of-way, railroads, pipelines, lumberyards, tank farms,
and similar areas. Controls broadleaf weeds and grasses
over an extended period of time
Environmental Fate
Soil. Degrades in soil yielding hydroxy metabolites and dealkylation of the side chains
(Hartley and Kidd, 1987).
Photolytic. Pelizzetti et al. (1990) studied the aqueous photocatalytic degradation of
prometon and other s-triazines (ppb level) using simulated sunlight (λ >340 nm) and
titanium dioxide as a photocatalyst. Prometon rapidly degraded forming cyanuric acid,
nitrates, the intermediate tentatively identified as 2,4-diamino-6-hydroxy-N,N′-bis(1-methylethyl)-1,3,5-triazine and other intermediate compounds similar to those found for atrazine. Mineralization of cyanuric acid to carbon dioxide was not observed (Pelizzetti et al.,
1990).
Shipping
UN2763 Triazine pesticides, solid, toxic, Hazard
Class: 6.1; Labels: 6.1-Poisonous materials.
Incompatibilities
Incompatible with oxidizers (chlorates,
nitrates, peroxides, permanganates, perchlorates, chlorine,
bromine, fluorine, etc.); contact may cause fires or explo-
sions. Keep away from alkaline materials, strong bases,
strong acids, oxoacids, epoxides. UV causes decomposition.
Waste Disposal
Dissolve or mix the material
with a combustible solvent and burn in a chemical
incinerator equipped with an afterburner and scrubber. All
federal, state, and local environmental regulations must be
observed. In accordance with 40CFR165, follow recom-
mendations for the disposal of pesticides and pesticide
containers. 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 1610-18-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,1 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1610-18:
(6*1)+(5*6)+(4*1)+(3*0)+(2*1)+(1*8)=50
50 % 10 = 0
So 1610-18-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H19N5O/c1-6(2)11-8-13-9(12-7(3)4)15-10(14-8)16-5/h6-7H,1-5H3,(H2,11,12,13,14,15)
1610-18-0Relevant articles and documents
Atrazine transformation using synthetic enzymes prepared by molecular imprinting.
Takeuchi, Toshifumi,Ugata, Satoshi,Masuda, Shuichi,Matsui, Jun,Yane, Takehisa,Takase, Masayoshi
, p. 2563 - 2566 (2007/10/03)
Atrazine imprinted synthetic polymers were prepared using a combination of methacrylic acid and 2-sulfoethyl methacrylate that bound and converted atrazine and other 6-chlorotriazine herbicides to less toxic compounds. A chloride at the 6-position of the triazines was converted to a methoxy group by the polymer in a methanol-containing solvent, where the imprinting effects enhanced the catalytic activity. Competitive inhibition of the atrazine methanolysis was observed in the presence of a structurally related binder, ametryn, suggesting that the catalytic reaction proceeded in the binding sites generated by the molecular imprinting process.
5,6-Dihydro-1,2,4,6-thiatriazin-5-one-1,1-dioxides
-
, (2008/06/13)
5,6-Dihydro-1,2,4,6-thiatriazin-5-one-1,1-dioxides of the formula STR1 where R1 is hydrogen, a metal atom or an unsubstituted or substituted ammonium radical, R2 is a saturated or unsaturated straight-chain aliphatic radical of up to 10 carbon atoms, a cycloaliphatic radical or 3 to 7 carbon atoms, a branched saturated or unsaturated aliphatic radical of 3 to 10 carbon atoms, a halogen-, alkoxy- or alkylmercapto-substituted aliphatic radical of 2 to 10 carbon atoms tetrahydrofuryl substituted methyl, a cycloalkoxy-substituted aliphatic radical of 4 to 10 carbon atoms, unsubstituted or halogen-substituted benzyl or phenyl, halophenyl, or alkylphenyl of a total of up to 10 carbon atoms, R3 is hydrogen, a straight-chain aliphatic radical of up to 10 carbon atoms, a cycloaliphatic radical of 3 to 7 carbon atoms, a branched aliphatic radical of 3 to 10 carbon atoms, haloalkyl, or alkoxyalkyl of 2 to 10 carbon atoms and X is oxygen and may also be sulfur if R2 is unsubstituted or halogen-substituted benzyl, processes for their preparation, and herbicides containing the above compounds.
4,5-Dichloroimidazole-2-carboxylic acid derivatives
-
, (2008/06/13)
4,5-Dichloroimidazole-2-carboxylic acid derivatives of the formula STR1 in which the group STR2 represents a carbon atom which has three bonds to hetero-atoms, and their salts with bases, possess insecticidal, acaricidal, fungicidal, nematicidal and herbicidal properties.
