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88-82-4 Usage

Chemical Properties

beige powder

Uses

2,3,5-Triiodobenzoic Acid is a polar auxin transport inhibitor that inhibits and promotes endoreduplication in hypocotyls and cotyledons.

Definition

ChEBI: A member of the class of benzoic acids that is benzoic acid in which the hydrogens at positions 2, 3 and 5 are replaced by iodine atoms. It is an auxin polar transport inhibitor.

Biochem/physiol Actions

2,3,5-Triiodobenzoic acid (TIBA) inhibits the translocation of indole-3-acetic acid transport.TIBA inhibits the colonization of the main root cortex by Laccaria bicolor S238 N and the formation of the Hartig net.

Check Digit Verification of cas no

The CAS Registry Mumber 88-82-4 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88-82:
(4*8)+(3*8)+(2*8)+(1*2)=74
74 % 10 = 4
So 88-82-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H3I3O2/c8-3-1-4(7(11)12)6(10)5(9)2-3/h1-2H,(H,11,12)/p-1

88-82-4 Well-known Company Product Price

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  • (Code)Product description
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  • Detail
  • TCI America

  • (T0451)  2,3,5-Triiodobenzoic Acid  >98.0%(HPLC)(T)

  • 88-82-4

  • 5g

  • 333.00CNY

  • Detail
  • TCI America

  • (T0451)  2,3,5-Triiodobenzoic Acid  >98.0%(HPLC)(T)

  • 88-82-4

  • 25g

  • 1,200.00CNY

  • Detail
  • Alfa Aesar

  • (L02679)  2,3,5-Triiodobenzoic acid, 98+%   

  • 88-82-4

  • 5g

  • 411.0CNY

  • Detail
  • Alfa Aesar

  • (L02679)  2,3,5-Triiodobenzoic acid, 98+%   

  • 88-82-4

  • 25g

  • 1226.0CNY

  • Detail
  • Alfa Aesar

  • (L02679)  2,3,5-Triiodobenzoic acid, 98+%   

  • 88-82-4

  • 100g

  • 3883.0CNY

  • Detail

88-82-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,5-triiodobenzoic acid

1.2 Other means of identification

Product number -
Other names 2,3,5-triiodo-benzoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:88-82-4 SDS

88-82-4Synthetic route

2-amino-3,5-diiodobenzoic acid
609-86-9

2-amino-3,5-diiodobenzoic acid

2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

Conditions
ConditionsYield
With potassium iodide Diazotization;
potassium anthranilate
37960-65-9

potassium anthranilate

2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: water; iodine
2: diluted hydrochloric acid; iodine monochloride
3: potassium iodide / Diazotization
View Scheme
anthranilic acid
118-92-3

anthranilic acid

2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: diluted hydrochloric acid; iodine monochloride
2: potassium iodide / Diazotization
View Scheme
2-amino-5-iodobenzoic acid
5326-47-6

2-amino-5-iodobenzoic acid

2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: diluted hydrochloric acid; iodine monochloride
2: potassium iodide / Diazotization
View Scheme
2-octylmethanesulfonate

2-octylmethanesulfonate

3-hydroxy-2,4,6-triiodo-benzoic acid ethyl ester
98589-35-6

3-hydroxy-2,4,6-triiodo-benzoic acid ethyl ester

2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

Conditions
ConditionsYield
With hydrogenchloride; potassium carbonate In ethyl acetate; N,N-dimethyl-formamide11.4 g (94%)
ethanol
64-17-5

ethanol

2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

2,3,5-triiodobenzoic acid ethyl ester
25546-12-7

2,3,5-triiodobenzoic acid ethyl ester

Conditions
ConditionsYield
With sulfuric acid Heating;95%
3-(tetrahydropyran-2'-yloxy)propyne
6089-04-9

3-(tetrahydropyran-2'-yloxy)propyne

2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

3-[(tetrahydro-2H-pyran-2-yloxy)methyl]-5,7-diiodoisocoumarin

3-[(tetrahydro-2H-pyran-2-yloxy)methyl]-5,7-diiodoisocoumarin

Conditions
ConditionsYield
Stage #1: 2,3,5-triiodobenzoic acid With potassium carbonate In N,N-dimethyl-formamide at 25℃; for 0.166667h; Inert atmosphere; Schlenk technique;
Stage #2: 3-(tetrahydropyran-2'-yloxy)propyne With copper(l) iodide In N,N-dimethyl-formamide at 25℃; for 16h; Inert atmosphere; Schlenk technique; regioselective reaction;
93%
2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

phenylacetylene
536-74-3

phenylacetylene

3-phenyl-5,7-diiodoisocoumarin

3-phenyl-5,7-diiodoisocoumarin

Conditions
ConditionsYield
Stage #1: 2,3,5-triiodobenzoic acid With potassium carbonate In N,N-dimethyl-formamide at 25℃; for 0.166667h; Inert atmosphere; Schlenk technique;
Stage #2: phenylacetylene With copper(l) iodide In N,N-dimethyl-formamide at 25℃; for 16h; Inert atmosphere; Schlenk technique; regioselective reaction;
89%
2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

2,3,5-triiodobenzoyl chloride
42860-33-3

2,3,5-triiodobenzoyl chloride

Conditions
ConditionsYield
With thionyl chloride85%
With thionyl chloride for 16h; Reflux;60%
With thionyl chloride In tetrahydrofuran for 0.666667h; Heating / reflux;49%
N-BOC-1,2-diaminoethane
57260-73-8

N-BOC-1,2-diaminoethane

2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

C14H17I3N2O3
819079-61-3

C14H17I3N2O3

Conditions
ConditionsYield
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; for 13.5h; Inert atmosphere; Cooling with ice;82%
With dmap; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide In dichloromethane
1-hydroxy-pyrrolidine-2,5-dione
6066-82-6

1-hydroxy-pyrrolidine-2,5-dione

2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

2,5-dioxopyrrolidin-1-yl 2,3,5-triiodobenzoate
161234-25-9

2,5-dioxopyrrolidin-1-yl 2,3,5-triiodobenzoate

Conditions
ConditionsYield
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 3h; Inert atmosphere;82%
2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

1-phenylbut-3-yn-1-ol
1743-36-8

1-phenylbut-3-yn-1-ol

3-(2-hydroxy-2-phenylethyl)-5,7-diiodoisocoumarin

3-(2-hydroxy-2-phenylethyl)-5,7-diiodoisocoumarin

Conditions
ConditionsYield
Stage #1: 2,3,5-triiodobenzoic acid With potassium carbonate In N,N-dimethyl-formamide at 25℃; for 0.166667h; Inert atmosphere; Schlenk technique;
Stage #2: 1-phenylbut-3-yn-1-ol With copper(l) iodide In N,N-dimethyl-formamide at 25℃; for 16h; Inert atmosphere; Schlenk technique; regioselective reaction;
81%
2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

benzoic-2,3,5-d3 acid
87976-29-2

benzoic-2,3,5-d3 acid

Conditions
ConditionsYield
With H2O*(2)H2O2P(1-)*Na(1+); α,α'-azodiizobutyramidine-dihydrochloride; sodium hydrogencarbonate In water at 80℃; for 8h; Inert atmosphere;81%
2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

1-amino-2,3,6,7,10,11-hexa(heptyloxy)triphenylene
221147-26-8

1-amino-2,3,6,7,10,11-hexa(heptyloxy)triphenylene

1-(2,3,5-triiodobenzoylamino)-2,3,6,7,10,11-hexaheptyloxytriphenylene

1-(2,3,5-triiodobenzoylamino)-2,3,6,7,10,11-hexaheptyloxytriphenylene

Conditions
ConditionsYield
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 25℃; for 9h;80%
2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

propargyl alcohol methyl ether
627-41-8

propargyl alcohol methyl ether

3-methoxymethyl-5,7-diiodoisocoumarin

3-methoxymethyl-5,7-diiodoisocoumarin

Conditions
ConditionsYield
Stage #1: 2,3,5-triiodobenzoic acid With potassium carbonate In N,N-dimethyl-formamide at 25℃; for 0.166667h; Inert atmosphere; Schlenk technique;
Stage #2: propargyl alcohol methyl ether With copper(l) iodide In N,N-dimethyl-formamide at 25℃; for 16h; Inert atmosphere; Schlenk technique; regioselective reaction;
77%
vitamin E
59-02-9

vitamin E

2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

α-tocopheryl 2,3,5-triiodobenzoate

α-tocopheryl 2,3,5-triiodobenzoate

Conditions
ConditionsYield
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 22h;75%
2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

2,2,6,6-tetramethylpiperidine-1-oxyl-4-yl 2,3,5-triiodobenzoate

2,2,6,6-tetramethylpiperidine-1-oxyl-4-yl 2,3,5-triiodobenzoate

Conditions
ConditionsYield
With dmap; dicyclohexyl-carbodiimide In dichloromethane; N,N-dimethyl-formamide at 0 - 20℃; for 26h; Inert atmosphere;75%
2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

thioacetic acid S-(2-acetylamino-phenyl)ester
1204-55-3

thioacetic acid S-(2-acetylamino-phenyl)ester

3-iodo-10H-phenothiazine-1-carboxylic acid

3-iodo-10H-phenothiazine-1-carboxylic acid

Conditions
ConditionsYield
With caesium carbonate In N,N-dimethyl-formamide at 130℃; for 10h; Inert atmosphere;75%
2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

C7H7ClF5O5S(1-)*C9H14N(1+)

C7H7ClF5O5S(1-)*C9H14N(1+)

C14H9F5I3O7S(1-)*C9H14N(1+)

C14H9F5I3O7S(1-)*C9H14N(1+)

Conditions
ConditionsYield
With potassium carbonate; sodium iodide In N,N-dimethyl-formamide at 90℃;71%
2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

Pregnenolone
145-13-1

Pregnenolone

pregnenolone 2,3,5-triiodobenzoat
97545-42-1

pregnenolone 2,3,5-triiodobenzoat

Conditions
ConditionsYield
With dmap; 2`,3`-dideoxycytidine In dichloromethane for 24h; Ambient temperature;69%
2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

phenylacetylene
536-74-3

phenylacetylene

A

1,4-diphenyl-1,3-butadiyne
886-66-8

1,4-diphenyl-1,3-butadiyne

B

3-phenyl-5,7-diiodoisocoumarin

3-phenyl-5,7-diiodoisocoumarin

Conditions
ConditionsYield
With copper(l) iodide; potassium carbonate In N,N-dimethyl-formamide at 50℃; Inert atmosphere; Schlenk technique;A 19%
B 68%
2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

1-(p-bromophenyl)-but-3-yn-1-ol
94612-95-0

1-(p-bromophenyl)-but-3-yn-1-ol

3-[2-(4-bromophenyl)-2-hydroxyethyl]-5,7-diiodoisocoumarin

3-[2-(4-bromophenyl)-2-hydroxyethyl]-5,7-diiodoisocoumarin

Conditions
ConditionsYield
Stage #1: 2,3,5-triiodobenzoic acid With potassium carbonate In N,N-dimethyl-formamide at 25℃; for 0.166667h; Inert atmosphere; Schlenk technique;
Stage #2: 1-(p-bromophenyl)-but-3-yn-1-ol With copper(l) iodide In N,N-dimethyl-formamide at 25℃; for 16h; Inert atmosphere; Schlenk technique; regioselective reaction;
68%
2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

8-bromooctyl acrylate
123563-83-7

8-bromooctyl acrylate

2,3,5-triiodobenzoic acid 8-acryloyloxyoctyl ester

2,3,5-triiodobenzoic acid 8-acryloyloxyoctyl ester

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 85℃; for 2.5h; Inert atmosphere; Sealed tube;66%
2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

hex-1-yne
693-02-7

hex-1-yne

3-butyl-5,7-diiodoisocoumarin

3-butyl-5,7-diiodoisocoumarin

Conditions
ConditionsYield
Stage #1: 2,3,5-triiodobenzoic acid With potassium carbonate In N,N-dimethyl-formamide at 25℃; for 0.166667h; Inert atmosphere; Schlenk technique;
Stage #2: hex-1-yne With copper(l) iodide In N,N-dimethyl-formamide at 25℃; for 16h; Inert atmosphere; Schlenk technique; regioselective reaction;
60%
dichloromethane
75-09-2

dichloromethane

2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

6,8-diiodo-4H-benzo[d][1,3]dioxin-4-one

6,8-diiodo-4H-benzo[d][1,3]dioxin-4-one

Conditions
ConditionsYield
With 8-quinolinol; copper diacetate; sodium hydrogencarbonate; potassium hydroxide In N,N-dimethyl-formamide at 110℃; for 12h;60%
2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

propargyl alcohol
107-19-7

propargyl alcohol

3-(hydroxymethyl)-5,7-diiodoisocoumarin

3-(hydroxymethyl)-5,7-diiodoisocoumarin

Conditions
ConditionsYield
Stage #1: 2,3,5-triiodobenzoic acid With potassium carbonate In N,N-dimethyl-formamide at 25℃; for 0.166667h; Inert atmosphere; Schlenk technique;
Stage #2: propargyl alcohol With copper(l) iodide In N,N-dimethyl-formamide at 25℃; for 16h; Inert atmosphere; Schlenk technique; regioselective reaction;
59%
2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

silver(I) acetate
563-63-3

silver(I) acetate

Ag(1+)*C6H2I3COO(1-)=C6H2I3COOAg
271790-47-7

Ag(1+)*C6H2I3COO(1-)=C6H2I3COOAg

Conditions
ConditionsYield
In methanol; water aq. soln. AgCH3COO was layered with methanolic soln. triiodobenzoic acid and was alloweed to stand at room temp. for 1 day; elem. anal.;57%
n-octyne
629-05-0

n-octyne

2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

3-hexyl-5,7-diiodoisocoumarin

3-hexyl-5,7-diiodoisocoumarin

Conditions
ConditionsYield
Stage #1: 2,3,5-triiodobenzoic acid With potassium carbonate In N,N-dimethyl-formamide at 25℃; for 0.166667h; Inert atmosphere; Schlenk technique;
Stage #2: n-octyne With copper(l) iodide In N,N-dimethyl-formamide at 25℃; for 16h; Inert atmosphere; Schlenk technique; regioselective reaction;
53%
1,7-Octadiyne
871-84-1

1,7-Octadiyne

2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

3-(hex-5-ynyl)-5,7-diiodoisocoumarin

3-(hex-5-ynyl)-5,7-diiodoisocoumarin

Conditions
ConditionsYield
Stage #1: 2,3,5-triiodobenzoic acid With potassium carbonate In N,N-dimethyl-formamide at 25℃; for 0.166667h; Inert atmosphere; Schlenk technique;
Stage #2: 1,7-Octadiyne With copper(l) iodide In N,N-dimethyl-formamide at 25℃; for 16h; Inert atmosphere; Schlenk technique; regioselective reaction;
38%
2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

C30H56NO12S(1-)*Na(1+)

C30H56NO12S(1-)*Na(1+)

C37H57I3NO13S(1-)*Na(1+)

C37H57I3NO13S(1-)*Na(1+)

Conditions
ConditionsYield
With pyridine; dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 18h;36.3%
2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

6-(aminooxy)-N-(triphenylmethoxy)hexanamide

6-(aminooxy)-N-(triphenylmethoxy)hexanamide

2,3,5-triiodo-N-((6-oxo-6-((trityloxy)amino)hexyl)oxy)benzamide

2,3,5-triiodo-N-((6-oxo-6-((trityloxy)amino)hexyl)oxy)benzamide

Conditions
ConditionsYield
Stage #1: 2,3,5-triiodobenzoic acid With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide for 0.25h;
Stage #2: 6-(aminooxy)-N-(triphenylmethoxy)hexanamide In N,N-dimethyl-formamide at 20℃; for 16h;
35%
2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

C47H96O9SSi3
1234307-18-6

C47H96O9SSi3

C54H97I3O10SSi3
1234307-24-4

C54H97I3O10SSi3

Conditions
ConditionsYield
With dmap; 2,2'-dipyridyl carbonate In dichloromethane at 20℃; for 48h;34.4%
Propiolaldehyde diethyl acetal
10160-87-9

Propiolaldehyde diethyl acetal

2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

3-diethoxymethyl-5,7-diiodoisocoumarin

3-diethoxymethyl-5,7-diiodoisocoumarin

Conditions
ConditionsYield
Stage #1: 2,3,5-triiodobenzoic acid With potassium carbonate In N,N-dimethyl-formamide at 25℃; for 0.166667h; Inert atmosphere; Schlenk technique;
Stage #2: Propiolaldehyde diethyl acetal With copper(l) iodide In N,N-dimethyl-formamide at 25℃; for 16h; Inert atmosphere; Schlenk technique; regioselective reaction;
32%
4,4-diethoxybut-1-yne
13397-78-9

4,4-diethoxybut-1-yne

2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

3-(2,2-diethoxyethyl)-5,7-diiodoisocoumarin

3-(2,2-diethoxyethyl)-5,7-diiodoisocoumarin

Conditions
ConditionsYield
Stage #1: 2,3,5-triiodobenzoic acid With potassium carbonate In N,N-dimethyl-formamide at 25℃; for 0.166667h; Inert atmosphere; Schlenk technique;
Stage #2: 4,4-diethoxybut-1-yne With copper(l) iodide In N,N-dimethyl-formamide at 25℃; for 16h; Inert atmosphere; Schlenk technique; regioselective reaction;
31%
1-undecyne
2243-98-3

1-undecyne

2,3,5-triiodobenzoic acid
88-82-4

2,3,5-triiodobenzoic acid

3-nonyl-5,7-diiodoisocoumarin

3-nonyl-5,7-diiodoisocoumarin

Conditions
ConditionsYield
Stage #1: 2,3,5-triiodobenzoic acid With potassium carbonate In N,N-dimethyl-formamide at 25℃; for 0.166667h; Inert atmosphere; Schlenk technique;
Stage #2: 1-undecyne With copper(l) iodide In N,N-dimethyl-formamide at 25℃; for 16h; Inert atmosphere; Schlenk technique; regioselective reaction;
30%

88-82-4Relevant articles and documents

X-ray contrast agent

-

, (2008/06/13)

The present invention refers to a phospholipid-based compound, that is a phospholipid to which an X-ray contrast-giving moiety has been covalently linked, liposomes comprising said compound as well as the use of said liposomes as a diagnostic or contrast agent.

Compositions of iodobenzoic acid derivatives and cellulose derivatives for visualization of the gastrointestinal tract

-

, (2008/06/13)

Disclosed are x-ray contrast compositions for oral or retrograde examination of the gastrointestinal tract comprising an x-ray producing agent of the formula or a pharmaceutically acceptable salt thereof STR1 wherein Z is H, halo, C1 -C20 alkyl, cycloalkyl, lower alkoxy, cyano, where the alkyl and cycloalkyl groups can be substituted with halogen or halo-lower-alkyl groups; R is C1 -C25 alkyl, cycloalkyl, or halo-lower-alkyl, each of which may be optionally substituted with halo, fluoro-lower-alkyl, aryl, lower-alkoxy, hydroxy, carboxy, lower-alkoxy carbonyl or lower-alkoxy-carbonyloxy; (CR1 R2)p -- (CR3 =CR4)m Q, or (CR1 R2)p -- C=C--Q; R1, R2, R3 and R4 are independently lower-alkyl, optionally substituted with halo; x is 1--3 y is 1--4; n is 1--5; m is 1--15; p is 1--10; and Q is H, lower-alkyl, lower-alkenyl, lower-alkynyl, lower-alkylene, aryl, or aryl-lower alkyl in a pharmaceutically acceptable carrier comprising a cellulose derivative.

Pesticide-polymer systems prepared from vinyl monomers

-

, (2008/06/13)

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.

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