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3653-48-3

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3653-48-3 Usage

Uses

Herbicide.

General Description

Colorless plates. Corrosive. Used as an herbicide.

Air & Water Reactions

Very soluble in water.

Reactivity Profile

MCPA SODIUM is a salt of a chlorinated benzoic acid.

Safety Profile

Poison by intraperitoneal route. Moderately toxic by ingestion and subcutaneous routes. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of Cland Na2O.

Check Digit Verification of cas no

The CAS Registry Mumber 3653-48-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,5 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3653-48:
(6*3)+(5*6)+(4*5)+(3*3)+(2*4)+(1*8)=93
93 % 10 = 3
So 3653-48-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H9ClO3.Na/c1-6-4-7(10)2-3-8(6)13-5-9(11)12;/h2-4H,5H2,1H3,(H,11,12);/q;+1/p-1

3653-48-3 Well-known Company Product Price

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  • Sigma-Aldrich

  • (45746)  MCPAsodiumsaltmonohydrate  PESTANAL®, analytical standard

  • 3653-48-3

  • 45746-250MG

  • 386.10CNY

  • Detail

3653-48-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name MCPA-sodium

1.2 Other means of identification

Product number -
Other names Dicotex

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:3653-48-3 SDS

3653-48-3Synthetic route

2-(4-chloro-2-methylphenoxy)ethanol
36220-29-8

2-(4-chloro-2-methylphenoxy)ethanol

sodium 2-methyl-4-chlorophenoxyacetate
3653-48-3

sodium 2-methyl-4-chlorophenoxyacetate

Conditions
ConditionsYield
With sodium hydroxide; oxygen; bismuth(III) nitrate; palladium on activated charcoal at 90℃; for 2h;98%
2-methyl-4-chlorophenol
1570-64-5

2-methyl-4-chlorophenol

sodium monochloroacetic acid
3926-62-3

sodium monochloroacetic acid

sodium 2-methyl-4-chlorophenoxyacetate
3653-48-3

sodium 2-methyl-4-chlorophenoxyacetate

Conditions
ConditionsYield
With sodium hydroxide In water for 8h; Reflux;
ortho-cresol
95-48-7

ortho-cresol

sodium 2-methyl-4-chlorophenoxyacetate
3653-48-3

sodium 2-methyl-4-chlorophenoxyacetate

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: potassium carbonate / toluene / 0.5 h / 120 °C
2: iron(III) chloride; tert-butyl methyl sulphide; thionyl chloride / 0.5 h / 40 °C
3: sodium hydroxide / 4 h / 70 °C
View Scheme
n-butyl o-tolyloxyacetate

n-butyl o-tolyloxyacetate

sodium 2-methyl-4-chlorophenoxyacetate
3653-48-3

sodium 2-methyl-4-chlorophenoxyacetate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: iron(III) chloride; tert-butyl methyl sulphide; thionyl chloride / 0.5 h / 40 °C
2: sodium hydroxide / 4 h / 70 °C
View Scheme
n-butyl 4-chloro-2-methylphenoxyacetate
1713-12-8

n-butyl 4-chloro-2-methylphenoxyacetate

sodium 2-methyl-4-chlorophenoxyacetate
3653-48-3

sodium 2-methyl-4-chlorophenoxyacetate

Conditions
ConditionsYield
With sodium hydroxide at 70℃; for 4h;223.74 g
C19H40NO(1+)*Cl(1-)
64632-18-4

C19H40NO(1+)*Cl(1-)

sodium 2-methyl-4-chlorophenoxyacetate
3653-48-3

sodium 2-methyl-4-chlorophenoxyacetate

cyclohexyldecyloxymethyldimethylammonium 4-chloro-2-methylphenoxyacetate
1616668-07-5

cyclohexyldecyloxymethyldimethylammonium 4-chloro-2-methylphenoxyacetate

Conditions
ConditionsYield
In water-d2 at 20℃; for 24h;98%
Cl(1-)*C13H28NO(1+)
64632-06-0

Cl(1-)*C13H28NO(1+)

sodium 2-methyl-4-chlorophenoxyacetate
3653-48-3

sodium 2-methyl-4-chlorophenoxyacetate

butoxymethylcyclohexyldimethylammonium 4-chloro-2-methylphenoxyacetate
1616668-04-2

butoxymethylcyclohexyldimethylammonium 4-chloro-2-methylphenoxyacetate

Conditions
ConditionsYield
In water-d2 at 20℃; for 24h;94%
C21H44NO(1+)*Cl(1-)
64632-17-3

C21H44NO(1+)*Cl(1-)

sodium 2-methyl-4-chlorophenoxyacetate
3653-48-3

sodium 2-methyl-4-chlorophenoxyacetate

cyclohexyldodecyloxymethyldimethylammonium 4-chloro-2-methylphenoxyacetate
1616668-08-6

cyclohexyldodecyloxymethyldimethylammonium 4-chloro-2-methylphenoxyacetate

Conditions
ConditionsYield
In water-d2 at 20℃; for 24h;94%
C15H32NO(1+)*Cl(1-)
64632-22-0

C15H32NO(1+)*Cl(1-)

sodium 2-methyl-4-chlorophenoxyacetate
3653-48-3

sodium 2-methyl-4-chlorophenoxyacetate

cyclohexylhexyloxymethyldimethylammonium 4-chloro-2-methylphenoxyacetate
1616668-05-3

cyclohexylhexyloxymethyldimethylammonium 4-chloro-2-methylphenoxyacetate

Conditions
ConditionsYield
In water-d2 at 20℃; for 24h;93%
sodium 2-methyl-4-chlorophenoxyacetate
3653-48-3

sodium 2-methyl-4-chlorophenoxyacetate

1-octyl-8-hydroxyquinolinium bromide

1-octyl-8-hydroxyquinolinium bromide

8-hydroxy-1-octyl-quinolinium (4-chloro-2-methylphenoxy)acetate
1082249-33-9

8-hydroxy-1-octyl-quinolinium (4-chloro-2-methylphenoxy)acetate

Conditions
ConditionsYield
In methanol for 12h;90%
C17H36NO(1+)*Cl(1-)
64632-20-8

C17H36NO(1+)*Cl(1-)

sodium 2-methyl-4-chlorophenoxyacetate
3653-48-3

sodium 2-methyl-4-chlorophenoxyacetate

cyclohexyldimethyloctyloxymethylammonium 4-chloro-2-methylphenoxyacetate
1616668-06-4

cyclohexyldimethyloctyloxymethylammonium 4-chloro-2-methylphenoxyacetate

Conditions
ConditionsYield
In water-d2 at 20℃; for 24h;90%
C23H48NO(1+)*Cl(1-)
1616668-18-8

C23H48NO(1+)*Cl(1-)

sodium 2-methyl-4-chlorophenoxyacetate
3653-48-3

sodium 2-methyl-4-chlorophenoxyacetate

cyclohexyldimethyltetradecyloxymethylammonium 4-chloro-2-methylphenoxyacetate
1616668-10-0

cyclohexyldimethyltetradecyloxymethylammonium 4-chloro-2-methylphenoxyacetate

Conditions
ConditionsYield
In water-d2 at 20℃; for 24h;86%
1,2,3-trimethyl-benzimidazolium; chloride
3653-04-1

1,2,3-trimethyl-benzimidazolium; chloride

sodium 2-methyl-4-chlorophenoxyacetate
3653-48-3

sodium 2-methyl-4-chlorophenoxyacetate

C10H13N2(1+)*C9H8ClO3(1-)

C10H13N2(1+)*C9H8ClO3(1-)

Conditions
ConditionsYield
In methanol at 65℃;71%
methanol
67-56-1

methanol

salicylhydroxamic acid
89-73-6

salicylhydroxamic acid

di-2-pyridyl ketone oxime
1562-95-4

di-2-pyridyl ketone oxime

nickel(II) chloride hexahydrate

nickel(II) chloride hexahydrate

sodium 2-methyl-4-chlorophenoxyacetate
3653-48-3

sodium 2-methyl-4-chlorophenoxyacetate

(Ni(II)(MCPA))2(12-MCNi(II)N(shi)2(pko)2-4)(12-MCNi(II)(shi)3(pko)-4)(MreOH)3(H2O)

(Ni(II)(MCPA))2(12-MCNi(II)N(shi)2(pko)2-4)(12-MCNi(II)(shi)3(pko)-4)(MreOH)3(H2O)

Conditions
ConditionsYield
With sodium methoxide In methanol salicylhydroxamic acid, di(2pyridyl)ketonoxime, excess MeONa and NaCl2*6H2O were dissolved in MeOH and stirred for 1 h, sodium salt MCPA was added; elem. anal.;60%
copper(II) nitrate

copper(II) nitrate

sodium 2-methyl-4-chlorophenoxyacetate
3653-48-3

sodium 2-methyl-4-chlorophenoxyacetate

copper(II) 2-methyl-4-chlorophenoxyacetate

copper(II) 2-methyl-4-chlorophenoxyacetate

Conditions
ConditionsYield
In water elem. anal.;
zinc(II) nitrate
10196-18-6

zinc(II) nitrate

sodium 2-methyl-4-chlorophenoxyacetate
3653-48-3

sodium 2-methyl-4-chlorophenoxyacetate

bis(2-methyl-4-chlorophenoxyacetato)tetra-aquozinc

bis(2-methyl-4-chlorophenoxyacetato)tetra-aquozinc

Conditions
ConditionsYield
With H2O In water double decompn. react. between zinc nitrate and the sodium butyrate in aq. soln.; elem. anal.;
With H2O In water ion exchange react. in aq. soln.; pptn.;
methanol
67-56-1

methanol

di-2-pyridyl ketone oxime
1562-95-4

di-2-pyridyl ketone oxime

nickel(II) chloride hexahydrate

nickel(II) chloride hexahydrate

Salicylhydroxamic acid
89-73-6

Salicylhydroxamic acid

sodium 2-methyl-4-chlorophenoxyacetate
3653-48-3

sodium 2-methyl-4-chlorophenoxyacetate

10Ni(2+)*5OC6H4C(O)NO(3-)*3ONC(C5H4N)2(1-)*2CH3C6H3(Cl)OCH2CO2(1-)*6.25CH3OH*2.2H2O=C92.25H89.4Cl2N14Ni10O32.45

10Ni(2+)*5OC6H4C(O)NO(3-)*3ONC(C5H4N)2(1-)*2CH3C6H3(Cl)OCH2CO2(1-)*6.25CH3OH*2.2H2O=C92.25H89.4Cl2N14Ni10O32.45

Conditions
ConditionsYield
With NaOH In methanol addn. of Na-salt of substituted phenoxyacetic acid to mixt. of other educts and NaOH; crystn. on slow evapn. (48 h); elem. anal.;
4-dodecyl-4-methyl-morpholine chloride
14866-50-3

4-dodecyl-4-methyl-morpholine chloride

sodium 2-methyl-4-chlorophenoxyacetate
3653-48-3

sodium 2-methyl-4-chlorophenoxyacetate

4-dodecyl-4-methyl-morpholine (4-chloro-2-methylphenoxy)acetate
1082249-21-5

4-dodecyl-4-methyl-morpholine (4-chloro-2-methylphenoxy)acetate

Conditions
ConditionsYield
In water at 20℃; for 24h;
3,5-diphenyl-1,2-dimethylpyrazolium chloride
53050-16-1

3,5-diphenyl-1,2-dimethylpyrazolium chloride

sodium 2-methyl-4-chlorophenoxyacetate
3653-48-3

sodium 2-methyl-4-chlorophenoxyacetate

3,5-diphenyl-1,2-dimethylpyrazolium (4-chloro-2-methylphenoxy)acetate

3,5-diphenyl-1,2-dimethylpyrazolium (4-chloro-2-methylphenoxy)acetate

Conditions
ConditionsYield
In water at 19.84℃; for 24h;
sodium 2-methyl-4-chlorophenoxyacetate
3653-48-3

sodium 2-methyl-4-chlorophenoxyacetate

MCPA
94-74-6

MCPA

Conditions
ConditionsYield
With hydrogenchloride In water pH=1;

3653-48-3Relevant articles and documents

Preparation method of phenoxycarboxylate herbicide

-

Paragraph 0075; 0078, (2019/01/08)

The invention provides a preparation method of a phenoxycarboxylate herbicide, wherein the preparation method includes the steps: S1, carrying out condensation reaction of phenol or o-cresol with chlorocarboxylic ester under the action of alkaline substances to obtain phenoxycarboxylic ester, wherein chlorocarboxylic ester has the general formula of ClR1COOR, R1 is C1-3 alkylene or alkylidene, R is C1-10 alkyl of or C3-10 cycloalkyl; and S2, under the action of a first catalyst and a second catalyst, carrying out selective chlorination of the phenoxycarboxylic ester with a chlorinating agent to obtain the chlorophenoxycarboxylic ester represented by the formula I, R3 is H, Cl or CH3, the first catalyst is selected from Lewis acid, and the second catalyst is selected from C5-22 thioether, thiazole, isothiazole or thiophene compounds; and S3, mixing chlorophenoxycarboxylic ester with an alkaline compound, and carrying out alkaline hydrolysis to obtain the phenoxycarboxylate herbicide. The preparation method can improve the product quality and production operation environment, and has low quantity of three wastes.

Process for preparing solid, free-flowing water-soluble salts of aryloxy-C1 -C4 -alkanecarboxylic acids

-

, (2008/06/13)

Process for preparing solid, free-flowing water-soluble salts of aryloxy-C1 -C4 -alkanecarboxylic acids by reacting the aryloxy-C1 -C4 -alkanecarboxylic acids with a salt-forming base, the salt formation taking place in the melt in the presence or absence of an entraining agent suitable for the azeotropic removal of water or in solution in the presence of an entraining agent suitable for the azeotropic removal of water and, if appropriate, removing the entraining agent from the reaction mixture during the reaction or subsequently and then isolating the solid salts in a customary manner.

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