1698-60-8

Usage

Uses

Used in Agriculture:
Poly (acrylic acid-co-hypophosphite) sodium salt is used as a herbicide for controlling weed growth in agricultural fields. It works by perturbing cell membranes, disrupting the normal functioning of the plant cells and ultimately leading to the death of the weed.
Used in Chemical Industry:
In the chemical industry, Poly (acrylic acid-co-hypophosphite) sodium salt can be utilized as a component in the formulation of various products due to its unique chemical properties, such as its ability to form complexes with other molecules and its reactivity with different chemical groups.
Used in Water Treatment:
Poly (acrylic acid-co-hypophosphite) sodium salt can be employed in water treatment processes as a flocculant or coagulant. Its ability to bind with impurities and form larger particles facilitates the removal of contaminants from water, making it a valuable asset in the water treatment industry.
Used in Pharmaceutical Industry:
The unique properties of Poly (acrylic acid-co-hypophosphite) sodium salt may also make it a potential candidate for use in the pharmaceutical industry, particularly in the development of drug delivery systems or as a component in the synthesis of new drugs.
Used in Environmental Applications:
Due to its ability to interact with various contaminants, Poly (acrylic acid-co-hypophosphite) sodium salt can be used in environmental applications for the remediation of polluted sites, such as soil and water treatment, by helping to remove or neutralize harmful substances.

Safety Profile

Moderately toxic by ingestion and intraperitoneal routes. A severe eye irritant. Experimental reproductive effects. Used as a preemergence and early post-emergence herbicide. When heated to decomposition it emits very toxic fumes of Cland NOx.

InChI:InChI=1/C10H8ClN3O/c11-9-8(12)6-13-14(10(9)15)7-4-2-1-3-5-7/h1-6H,12H2

Upstream product

• 1698-53-9 4,5-dichloro-1-phenylpyridazin-6-one 
• 99-96-7 4-hydroxy-benzoic acid 
• 98-67-9 p-hydoroxybenzenesulfonic acid 
• 156-38-7 4-hydroxyphenylacetate 
• 80-09-1 4,4'-sulfonediphenol 
• 100-02-7 4-nitro-phenol 
• 611-99-4 4,4'-Dihydroxybenzophenone 

Downstream Products

• 1698-53-9 4,5-dichloro-1-phenylpyridazin-6-one 
• 30578-37-1 4-amino-6-methoxy-1-phenyl-pyridazinium methyl sulfate 
• 13589-77-0 5-amino-2-phenyl-3(2H)-pyridazinone 
• 113478-90-3 4-(5-Chloro-6-oxo-1-phenyl-1,6-dihydro-pyridazin-4-yl-diazenyl)-6-phenyl-3-thioxo-3,4-dihydro-2H-[1,2,4]triazin-5-one 
• 136353-42-9 6-Phenyl-2-p-tolylamino-6H-thiazolo[4,5-d]pyridazin-7-one 
• 136353-41-8 2-(4-Ethoxy-phenylamino)-6-phenyl-6H-thiazolo[4,5-d]pyridazin-7-one 
• 67322-81-0 2-methyl-1,1,4-trioxo-1,2,3,4-tetrahydro-1λ⁶-benzo[e][1,2]thiazine-3-carboxylic acid 5-chloro-6-oxo-1-phenyl-1,6-dihydro-pyridazin-4-ylamide 
• 3137-31-3 6-phenyl-2-thioxo-2,3-dihydro-6H-thiazolo[4,5-d]pyridazin-7-one 
• 52112-91-1 2-hydrazino-6-phenyl-6H-thiazolo[4,5-d]pyridazin-7-one 
• 3042-95-3 2-methylsulfanyl-6-phenyl-6H-thiazolo[4,5-d]pyridazin-7-one 

Relevant academic research and scientific papers

Method for producing 4-amino-5-chloro-1-phenyl pyridazinone-(6)

In a process for preparing 4-amino-5-chloro-1-phenylpyridazin-6-one by reacting 4,5-dichloro-1-phenylpyridazin-6-one with aqueous ammonia in the presence of a catalyst, the catalyst used is soluble in the aqueous alkaline reaction medium but is essentially insoluble in the reaction medium which has been acidified after removal of the 4-amino-5-chloro-1-phenylpyridazin-6-one. The process of the present invention makes it possible for the catalyst to be recovered and reused in a simple manner.

Substituted pyridinesulfonamide compound or its salt, process for preparing the same, and herbicide containing the same

A substituted pyridinesulfonamide compound or its salt represented by the following general formula (I): STR1 wherein A is CH or N; when A is CH, R1 and R2 may be either each independently a member selected from the group consisting of unsubstituted or substituted alkyl groups, unsubstituted or substituted alkenyl groups, unsubstituted or substituted cycloalkyl groups, and unsubstituted or substituted phenyl groups; when A is N, R1 is an unsubstituted or substituted alkyl group, R2 is an unsubstituted or substituted alkyl group, or an unsubstituted or substituted alkoxy group; and X and Y are each independently a member selected from the group consisting of alkyl groups and alkoxy groups, is disclosed. This compound is useful as the effective ingredient of a herbicide showing a wide weed-control spectrum even if used in a small amount.

Substituted pyridinesulfonamide compounds or their salts, process for preparing the same, and herbicides containing the same

A substituted pyridinesulfonamide compound or its salt represented by the following general formula (I): wherein R1 is an unsubstituted or substituted alkyl group; R2 is an unsubstituted or substituted alkyl group, or an unsubstituted or substituted alkoxy group; and X and Y are each independently a member selected from the group consisting of alkyl groups and alkoxy groups, is disclosed. This compound is useful as the effective ingredient of a herbicide showing a wide weed-control spectrum even if used in a small amount.

Controlled release pesticides

Controlled release pesticide-polymers are prepared by reacting a polymer having a pendant group containing a reactive hydrogen with a chloroformamide derivative of a pesticide. In a preferred embodiment, metribuzin chloroformamide is prepared by reacting metribuzin with phosgene at a temperature of about 40° C. The metribuzin chloroformamide is then reacted with cellulose to form a pesticide-polymer from which the metribuzin is released under use conditions by hydrolytic degradation of the carbamate bond attaching the metribuzin to the polymer.

SYNTHESIS, SPECTRAL PROPERTIES, AND PESTICIDAL ACTIVITY OF 4-AMINO(ALKYLAMINO, DIALKYLAMINO)-5-CHLORO-2-SUBSTITUTED-3-OXO-2H-PYRIDAZINES AND 5-AMINO(ALKYLAMINO, DIALKYLAMINO)-4-CHLORO-2-SUBSTITUTED-3-OXO-2H-PYRIDAZINES

4-Amino(alkylamino)-5-chloro-2-substituted-3-oxo-2H-pyridazines and 5-amino(alkylamino, dialkylamino)-4-chloro-2-substituted-3-oxo-2H-pyridazines have been prepared by nucleophilic substitution reactions of 4,5-dichloro-2-substituted-3-oxo-2H-pyridazines with amines in aprotic solvent.Structure of the compounds prepared has been proved by IR and UV spectra.Fungicidal and herbicidal activity of the compounds prepared have been tested.None of the compounds prepared exceeds the standard Vitavax in the fungicidal activity tests.Compounds VIII and XII show equal or better activity on the Hill reaction as compared with the standard pyrazone.

Method for producing 4-chloro-5-amino-2-phenyl-3(2H)-pyridazinone from 4,5-dichloro-2-phenyl-3(2H)-pyridazione and ammonia

4-Chloro-5-amino-2-phenyl-3(2H)-pyridazinone is prepared from 4,5-dichloro-2-phenyl-3(2H)-pyridazinone and ammonia in high yield and substantially free from 4-amino-5-chloro-2-phenyl-3(2 H)-pyridazinone in a method comprising reacting 4,5-dichloro-2-phenyl-3(2H)-pyridazinone with aqueous ammonia in the presence of a catalyst which is capable of selectively exchanging the 5-chlorine atom in 4,5-dichloro-2-phenyl-3(2H)-pyridazinone with a leaving group of such a nature that the resulting intermediate compound is capable of alkylating ammonia to 4-chloro-5-amino-2-phenyl-3(2H)-pyridazinone in high yield in the reaction medium, thereby regenerating the catalyst. The end product is isolated by filtration after the reaction and washed with water, and the mother liquor plus the wash water are used as reaction medium for the next batch.

5,6-Dihydro-1,2,4,6-thiatriazin-5-one-1,1-dioxides

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.

Pesticide-polymer systems prepared from vinyl monomers

Controlled release pesticide-polymer systems are prepared by the polymerization of vinyl monomers containing pendant pesticides. The vinyl monomers are prepared by reacting an acrylic acid derivative with a pesticide or a pesticide derivative having an active hydrogen. The pesticide-polymer systems prepared from the pesticide vinyl monomers release the active pesticide material by hydrolysis or chemical depolymerization under conditions of use.

4,5-Dichloroimidazole-2-carboxylic acid derivatives

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.