Product Name

  • Name

    2,4-Pyridinedicarboxylic acid

  • EINECS 207-892-2
  • CAS No. 499-80-9
  • Article Data23
  • CAS DataBase
  • Density 1.551 g/cm3
  • Solubility Soluble in water at 20°C 4.5 g/L.
  • Melting Point 243-246 °C
  • Formula C7H5NO4
  • Boiling Point 574.8 °C at 760 mmHg
  • Molecular Weight 167.121
  • Flash Point 301.4 °C
  • Transport Information
  • Appearance white to off-white crystalline powder
  • Safety 24/25-26
  • Risk Codes 36/37/38
  • Molecular Structure Molecular Structure of 499-80-9 (2,4-Pyridinedicarboxylic acid)
  • Hazard Symbols IrritantXi
  • Synonyms 2,4-Dicarboxylpyridine;2,4-Lutidinic acid;Lutidinic acid;NSC 403248;
  • PSA 87.49000
  • LogP 0.47800

Synthetic route

2,4-lutidine
108-47-4

2,4-lutidine

pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

Conditions
ConditionsYield
With 18-crown-6 ether; potassium tert-butylate; oxygen In 1,2-dimethoxyethane at 60℃; under 3800 Torr; for 48h;52%
With potassium permanganate
With permanganate(VII) ion
2-ethyl-4-methylpyridine
2150-18-7

2-ethyl-4-methylpyridine

pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

Conditions
ConditionsYield
With permanganate(VII) ion
4-ethyl-2-methyl-pyridine
536-88-9

4-ethyl-2-methyl-pyridine

pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

Conditions
ConditionsYield
With permanganate(VII) ion
2.2'-dimethyl-dipyridyl-(4.4')

2.2'-dimethyl-dipyridyl-(4.4')

pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

Conditions
ConditionsYield
With permanganate(VII) ion
2-methyl-pyridine-carboxylic acid-(4)

2-methyl-pyridine-carboxylic acid-(4)

pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

Conditions
ConditionsYield
With alkaline permanganate solution
crude lutidine

crude lutidine

pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

Conditions
ConditionsYield
With permanganate(VII) ion
2,4-lutidine
108-47-4

2,4-lutidine

sulfuric acid
7664-93-9

sulfuric acid

selenium

selenium

A

2-methylisonicotinic acid
4021-11-8

2-methylisonicotinic acid

B

pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

Conditions
ConditionsYield
at 300℃;
2-carbamoyl-4-cyanopyridine
54089-05-3

2-carbamoyl-4-cyanopyridine

pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

Conditions
ConditionsYield
With sodium hydroxide In water
3-methoxy-4-hydroxybenzoic acid
121-34-6

3-methoxy-4-hydroxybenzoic acid

pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

Conditions
ConditionsYield
With thiostrepton; ammonium chloride at 30℃; for 168h;
With disodium hydrogenphosphate; potassium dihydrogenphosphate; chloramphenicol; magnesium sulfate; ammonium chloride; thiostrepton A; sodium chloride; calcium chloride In water at 30℃; for 168h; Reagent/catalyst; Enzymatic reaction;
lignocellulose

lignocellulose

pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

Conditions
ConditionsYield
With thiostrepton; ammonium chloride at 30℃; for 168h; Time;
Kraft lignin

Kraft lignin

pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

Conditions
ConditionsYield
With thiostrepton; ammonium chloride at 30℃; for 96h;
With disodium hydrogenphosphate; potassium dihydrogenphosphate; chloramphenicol; magnesium sulfate; ammonium chloride; thiostrepton A; sodium chloride; calcium chloride In water at 30℃; for 96h; Flow reactor; Enzymatic reaction;
wheat straw lignocellulose

wheat straw lignocellulose

pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

Conditions
ConditionsYield
With disodium hydrogenphosphate; potassium dihydrogenphosphate; chloramphenicol; magnesium sulfate; ammonium chloride; thiostrepton A; sodium chloride; calcium chloride In water at 30℃; for 216h; Flow reactor; Enzymatic reaction;
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

ethanol
64-17-5

ethanol

diethyl pyridine-2,4-dicarboxylate
41438-38-4

diethyl pyridine-2,4-dicarboxylate

Conditions
ConditionsYield
With toluene-4-sulfonic acid for 24h; Heating;100%
With toluene-4-sulfonic acid In toluene at 110℃;88%
Stage #1: ethanol With thionyl chloride at 0℃; for 0.5h; Inert atmosphere;
Stage #2: pyridine-2,4-dicarboxylic acid In ethanol for 3h; Inert atmosphere; Reflux;
82%
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

ethanol
64-17-5

ethanol

2-(ethoxycarbonyl)isonicotinic acid
142074-49-5

2-(ethoxycarbonyl)isonicotinic acid

Conditions
ConditionsYield
With toluene-4-sulfonic acid at 80℃; Fischer-Speier Esterification; Inert atmosphere;100%
at 80℃; Acidic conditions;
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

zinc(II) acetate tetrahydrate

zinc(II) acetate tetrahydrate

zinc 4-carboxypicolinate

zinc 4-carboxypicolinate

Conditions
ConditionsYield
In ethanol; water99.3%
fac-triaquatricarbonyltechnetium-99m(1+)

fac-triaquatricarbonyltechnetium-99m(1+)

pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

[(99)Tc(OH2)(4-carboxypyridine-2-carboxylato)(CO)3]

[(99)Tc(OH2)(4-carboxypyridine-2-carboxylato)(CO)3]

Conditions
ConditionsYield
In water a soln. of acid in water was added to the freshly prepared soln. of complex, the mixt. was stirred at 90°C for 45 min; cooled on ice bath, HPLC analyses;99%
In water
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

water
7732-18-5

water

copper(II) acetate monohydrate
6046-93-1

copper(II) acetate monohydrate

[Cu(pyridine-2,4-dicarboxylic acid(-1H))2(H2O)2]
363176-04-9, 831196-27-1

[Cu(pyridine-2,4-dicarboxylic acid(-1H))2(H2O)2]

Conditions
ConditionsYield
In water 70°C; elem. anal.;99%
4-aminopyridine
504-24-5

4-aminopyridine

pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

N-(pyridin-4-yl)isonicotinamide

N-(pyridin-4-yl)isonicotinamide

Conditions
ConditionsYield
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃;99%
methanol
67-56-1

methanol

pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

pyridine-2,4-dicarboxylic acid dimethyl ester
25658-36-0

pyridine-2,4-dicarboxylic acid dimethyl ester

Conditions
ConditionsYield
With thionyl chloride for 5h; Reflux;98%
With phosphorus pentachloride at 20℃; for 0.75h;96%
With thionyl chloride at 65℃; for 10h;90%
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

N-methylaniline
100-61-8

N-methylaniline

pyridine-2,4-dicarboxylic acid bis-(N-methyl-anilide)
94870-72-1

pyridine-2,4-dicarboxylic acid bis-(N-methyl-anilide)

Conditions
ConditionsYield
Stage #1: pyridine-2,4-dicarboxylic acid With thionyl chloride for 12h; Reflux;
Stage #2: N-methylaniline With dmap; triethylamine In dichloromethane at 0 - 20℃;
97%
1,4-dioxane
123-91-1

1,4-dioxane

pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

2–(2–(2–chloroethoxy)ethoxy)isonicotinic acid

2–(2–(2–chloroethoxy)ethoxy)isonicotinic acid

Conditions
ConditionsYield
With tert-butylhypochlorite; chloranil at 110℃; for 30h; Inert atmosphere;93%
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

uranyl nirate hexahydrate

uranyl nirate hexahydrate

cadmium(II) nitrate tetrhydrate

cadmium(II) nitrate tetrhydrate

O2U(2+)*2C7H3NO4(2-)*Cd(2+)

O2U(2+)*2C7H3NO4(2-)*Cd(2+)

Conditions
ConditionsYield
With perchloric acid at 120℃; for 72h;90%
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

potassium tetrachloropalladate(II)
10025-98-6

potassium tetrachloropalladate(II)

cobalt(II) chloride hydrate

cobalt(II) chloride hydrate

potassium hydroxide

potassium hydroxide

3Co(2+)*2Pd(2+)*4C5H3N(COO)2(2-)*2OH(1-)*4H2O=[Co3Pd2(OH)2(C5H3N(COO)2)4]*4H2O

3Co(2+)*2Pd(2+)*4C5H3N(COO)2(2-)*2OH(1-)*4H2O=[Co3Pd2(OH)2(C5H3N(COO)2)4]*4H2O

Conditions
ConditionsYield
In water High Pressure; aq. soln. of Pd complex, dicarboxylic acid, and 1M KOH mixed; aq. soln. of metal chloride added (Pd:metal:ligand:base = 1:2:2:6); heated in a Teflon-lined autoclave at 200°C for 15 h, cooled to room temp. overa period of 8 h; ppt. filtered off, washed (H2O), dried; elem. anal.;89%
copper(ll) sulfate pentahydrate

copper(ll) sulfate pentahydrate

pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

water
7732-18-5

water

[Cu(pyridine-2,4-dicarboxylic acid(-1H))2(H2O)2]
363176-04-9, 831196-27-1

[Cu(pyridine-2,4-dicarboxylic acid(-1H))2(H2O)2]

Conditions
ConditionsYield
In methanol; water MeOH soln. of ligand (2 equiv.) added to aq. soln. of Cu salt; filtered; ppt. washed with MeOH; dried under vac. for 1 h; elem. anal.;88%
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

cadmium(II) nitrate tetrhydrate

cadmium(II) nitrate tetrhydrate

hydrazine hydrate
7803-57-8

hydrazine hydrate

[Cd(pyridine-2,4-dicarboxylic acid-2H)(hydrazine)(H2O)]*H2O

[Cd(pyridine-2,4-dicarboxylic acid-2H)(hydrazine)(H2O)]*H2O

Conditions
ConditionsYield
In water by addn. of an aq. soln. of a ligand (0.5 mmol) and hydrazine hydrate (2mmol) to the aq. soln. of metal nitrate hydrate (0.5 mmol); the ppt. was collected, washed with water, ethanol, and diethyl ether, and air-dried; elem. anal.;88%
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

copper(II) nitrate trihydrate

copper(II) nitrate trihydrate

terbium(III) nitrate hexahydrate

terbium(III) nitrate hexahydrate

[Tb2Cu3(pyridine-2,4-dicarboxylic acid-2H)6(H2O)6]n

[Tb2Cu3(pyridine-2,4-dicarboxylic acid-2H)6(H2O)6]n

Conditions
ConditionsYield
In water High Pressure; a mixt. of Tb-contg. compd. (0.1 mmol), Cu-contg. compd. (0.15 mmol) anda ligand (0.3 mmol) in H2O was sealed in a Teflon-lined bomb at 160.deg ree.C for 6 d; slow cooling to room temp. by 5°C/h; crystals were recovered by filtration, washed by distd. water, and air-dried; elem. anal.;87%
Creatinine
60-27-5

Creatinine

pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

cobalt(II) chloride hexahydrate

cobalt(II) chloride hexahydrate

(creatinine)2[Co(Pyridine-2,4-dicarboxylic acid(-2H))2(H2O)2]*2H2O

(creatinine)2[Co(Pyridine-2,4-dicarboxylic acid(-2H))2(H2O)2]*2H2O

Conditions
ConditionsYield
Stage #1: Creatinine; pyridine-2,4-dicarboxylic acid In water at 80℃; for 1h;
Stage #2: cobalt(II) chloride hexahydrate In water at 80℃; for 1h;
85.54%
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

water
7732-18-5

water

copper(II) acetate monohydrate
6046-93-1

copper(II) acetate monohydrate

trans-1,2-bis(pyridin-4-yl)ethene
13362-78-2

trans-1,2-bis(pyridin-4-yl)ethene

[Cu(2,4-pyridinedicarboxylate)(trans-1,2-bis(4-pyridyl)ethylene)2]*3H2O

[Cu(2,4-pyridinedicarboxylate)(trans-1,2-bis(4-pyridyl)ethylene)2]*3H2O

Conditions
ConditionsYield
With Et3N In methanol; water aq. soln. of copper compd. mixed with soln. of pyridinedicarboxylic acidand Et3N (1:1:2), stirred for 15 min, methanolic soln. of bpe (2 equiv. )added; stored for several d at room temp., crystd., elem. anal.;85%
(2-aminomethylpyridine)
3731-51-9

(2-aminomethylpyridine)

pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

copper(II) nitrate trihydrate

copper(II) nitrate trihydrate

water
7732-18-5

water

[Cu(pyridine-2,4-dicarboxylate)(2-picolylamine)(H2O)]*H2O

[Cu(pyridine-2,4-dicarboxylate)(2-picolylamine)(H2O)]*H2O

Conditions
ConditionsYield
Stage #1: pyridine-2,4-dicarboxylic acid; copper(II) nitrate trihydrate; water With triethylamine In methanol for 0.166667h;
Stage #2: 2-(Aminomethyl)pyridine In methanol for 1h; pH=Ca. 7 - 8; Reflux;
84%
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

copper(II) nitrate trihydrate

copper(II) nitrate trihydrate

erbium(III) nitrate hexahydrate

erbium(III) nitrate hexahydrate

[Er2Cu3(pyridine-2,4-dicarboxylic acid-2H)6(H2O)6]n

[Er2Cu3(pyridine-2,4-dicarboxylic acid-2H)6(H2O)6]n

Conditions
ConditionsYield
In water High Pressure; a mixt. of Er-contg. compd. (0.1 mmol), Cu-contg. compd. (0.15 mmol) anda ligand (0.3 mmol) in H2O was sealed in a Teflon-lined bomb at 160.deg ree.C for 6 d; slow cooling to room temp. by 5°C/h; crystals were recovered by filtration, washed by distd. water, and air-dried; elem. anal.;83%
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

potassium tetrachloropalladate(II)
10025-98-6

potassium tetrachloropalladate(II)

zinc(II) chloride hydrate

zinc(II) chloride hydrate

potassium hydroxide

potassium hydroxide

3Zn(2+)*2Pd(2+)*4C5H3N(COO)2(2-)*2OH(1-)*4H2O=[Zn3Pd2(OH)2(C5H3N(COO)2)4]*4H2O

3Zn(2+)*2Pd(2+)*4C5H3N(COO)2(2-)*2OH(1-)*4H2O=[Zn3Pd2(OH)2(C5H3N(COO)2)4]*4H2O

Conditions
ConditionsYield
In water High Pressure; aq. soln. of Pd complex, dicarboxylic acid, and 1M KOH mixed; aq. soln. of metal chloride added (Pd:metal:ligand:base = 1:2:2:6); heated in a Teflon-lined autoclave at 200°C for 15 h, cooled to room temp. overa period of 8 h; ppt. filtered off, washed (H2O), dried; elem. anal.;82%
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

palladium dichloride

palladium dichloride

Pd(NC5H3(COO)(COOH))2*3H2O

Pd(NC5H3(COO)(COOH))2*3H2O

Conditions
ConditionsYield
In sulfuric acid dissoln. on heating; ppt. filtration off, washing, drying (over CaCl2); elem. anal.;82%
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

nickel(II) nitrate hexahydrate

nickel(II) nitrate hexahydrate

hydrazine hydrate
7803-57-8

hydrazine hydrate

[Ni(pyridine-2,4-dicarboxylic acid-2H)(hydrazine)]*3H2O

[Ni(pyridine-2,4-dicarboxylic acid-2H)(hydrazine)]*3H2O

Conditions
ConditionsYield
In water by addn. of an aq. soln. of a ligand and hydrazine hydrate to the aq. soln. of metal nitrate hydrate (1:1:6 molar ratio of Ni nitrate, acid, andhydrazine hydrate); the ppt. was collected, washed with water, ethanol, and diethyl ether, and air-dried; elem. anal.;79%
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

(NEt4)2[rhenium(I)(bromide)3(carbonyl)3]

(NEt4)2[rhenium(I)(bromide)3(carbonyl)3]

fac-[Re(CO)3(2,4-pyridinedicarboxylate(1-))(H2O)]

fac-[Re(CO)3(2,4-pyridinedicarboxylate(1-))(H2O)]

Conditions
ConditionsYield
With AgNO3 In water byproducts: AgBr; to soln. Re complex in water (pH 2.2) AgNO3 was added, stirred at room temp. for 24 h, soln. was filtered, 2,4-pyridinedicarboxylic acid was added, stirred for 36 h; ppt. was filtered off and dried; elem. anal.;79%
potassium tetrachloroplatinate(II)
10025-99-7

potassium tetrachloroplatinate(II)

pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

cobalt(II) chloride hydrate

cobalt(II) chloride hydrate

potassium hydroxide

potassium hydroxide

3Co(2+)*2Pt(2+)*4C5H3N(COO)2(2-)*2OH(1-)*4H2O=[Co3Pt2(OH)2(C5H3N(COO)2)4]*4H2O

3Co(2+)*2Pt(2+)*4C5H3N(COO)2(2-)*2OH(1-)*4H2O=[Co3Pt2(OH)2(C5H3N(COO)2)4]*4H2O

Conditions
ConditionsYield
In water High Pressure; aq. soln. of Pt complex, dicarboxylic acid, and 1M KOH mixed; aq. soln. of metal chloride added (Pt:metal:ligand:base = 1:2:2:7); heated in a Teflon-lined autoclave at 200°C for 15 h, cooled to room temp. overa period of 8 h; ppt. filtered off, washed (H2O), dried; elem. anal.;78%
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

water
7732-18-5

water

nickel
7440-02-0

nickel

[Ni(2,4-pyridinedicarboxylate)(H2O)2]

[Ni(2,4-pyridinedicarboxylate)(H2O)2]

Conditions
ConditionsYield
In water High Pressure; hydrothermal conditions; mixt. of Ni powder and 2,4-pyridinedicarboxylicacid (molar ratio 1.5:1) in H2O placed in stainless steel autoclave; he ated at 170°C under autogenous pressure for 3 d; cooled to room temp. (5°C/h); crystals isolated; elem. anal.;78%
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

manganese(II) chloride tetrahydrate

manganese(II) chloride tetrahydrate

copper dichloride

copper dichloride

[CuMn(pyridine-2,5-dicarboxylate)2]

[CuMn(pyridine-2,5-dicarboxylate)2]

Conditions
ConditionsYield
With KOH In water High Pressure; 2 equiv. of the N-compd. in 1.0 M KOH and H2O were added to a CuCl2 soln., 1 equiv. of aq. MnCL2 was added to this soln., Cu:OH:ratio was 1:4, teflon-lined steel autoclave, 200 °C for 17 h; cooling to room temp. over 10 mins, crystals were filtered off, elem. anal.;78%
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

cobalt(II) chloride hexahydrate

cobalt(II) chloride hexahydrate

potassium hydroxide

potassium hydroxide

[Co3(pyridine-2,4-dicarboxylate)2(μ3-OH)2]*9H2O

[Co3(pyridine-2,4-dicarboxylate)2(μ3-OH)2]*9H2O

Conditions
ConditionsYield
In water at 199.84℃; for 0.5h; pH=8; Time; Microwave irradiation;78%
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

[Re2Cl4(μ-bis(diphenylphosphino)methane)2]
58298-10-5

[Re2Cl4(μ-bis(diphenylphosphino)methane)2]

dichloromethane
75-09-2

dichloromethane

benzene
71-43-2

benzene

Re2[η2(N,O)-O2C-2-C5H3N(-4-COOH)]Cl3(μ-Ph2PCH2PPh2)2*CH2Cl2*C6H6

Re2[η2(N,O)-O2C-2-C5H3N(-4-COOH)]Cl3(μ-Ph2PCH2PPh2)2*CH2Cl2*C6H6

Conditions
ConditionsYield
In ethanol mixt. Re2Cl4(μ-dppm)2 and pyridine-2,4-dicarboxylic acid in EtOH was refluxed for 24 h; react. mixt. was filtered, residue was washed with EtOH and Et2O and dried in vacuo, recrystn. from benzene-CH2Cl2; elem. anal.;77%
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

dysprosium(III) chloride hexahydrate

dysprosium(III) chloride hexahydrate

[Dy(PDC)2(H2O)2]*5H2O*NH4

[Dy(PDC)2(H2O)2]*5H2O*NH4

Conditions
ConditionsYield
With sodium hydroxide In dimethyl sulfoxide at 159.99℃; for 96h; Sealed tube;77%
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

potassium tetrachloropalladate(II)
10025-98-6

potassium tetrachloropalladate(II)

nickel(II) dichloride hydrate

nickel(II) dichloride hydrate

potassium hydroxide

potassium hydroxide

3Ni(2+)*2Pd(2+)*4C5H3N(COO)2(2-)*2OH(1-)*4H2O=[Ni3Pd2(OH)2(C5H3N(COO)2)4]*4H2O

3Ni(2+)*2Pd(2+)*4C5H3N(COO)2(2-)*2OH(1-)*4H2O=[Ni3Pd2(OH)2(C5H3N(COO)2)4]*4H2O

Conditions
ConditionsYield
In water High Pressure; aq. soln. of Pd complex, dicarboxylic acid, and 1M KOH mixed; aq. soln. of metal chloride added (Pd:metal:ligand:base = 1:2:2:6); heated in a Teflon-lined autoclave at 200°C for 15 h, cooled to room temp. overa period of 8 h; ppt. filtered off, washed (H2O), dried; elem. anal.;75%
pyridine-2,4-dicarboxylic acid
499-80-9

pyridine-2,4-dicarboxylic acid

copper nitrate hemi(pentahydrate)

copper nitrate hemi(pentahydrate)

Cu(C5H3N(CO2)2H)2*2H2O

Cu(C5H3N(CO2)2H)2*2H2O

Conditions
ConditionsYield
With KOH; H2O In water A mixt. of Cu-salt, acid, KOH (pH 3) and H2O was heated at 180°C for 3 days, cooled to room temp. by air-cooling; ppt. was filtered, washed with H2O and air-dried; elem. anal.;75%

2,4-Pyridinedicarboxylic acid Specification

The 2,4-Pyridinedicarboxylic acid, with the CAS registry number 499-80-9, is also known as Lutidinic acid. Its EINECS registry number is 207-892-2. This chemical's molecular formula is C7H5NO4 and molecular weight is 167.12. What's more, both its IUPAC name and systematic name are the same which is called Pyridine-2,4-dicarboxylic acid. It is used as organic synthetic reagent.

Physical properties about 2,4-Pyridinedicarboxylic acid are: (1)ACD/LogP: -0.20; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -3.84; (4)ACD/LogD (pH 7.4): -4.34; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 1; (8)ACD/KOC (pH 7.4): 1; (9)#H bond acceptors: 5; (10)#H bond donors: 2; (11)#Freely Rotating Bonds: 2; (12)Polar Surface Area: 65.49 Å2; (13)Index of Refraction: 1.627; (14)Molar Refractivity: 38.2 cm3; (15)Molar Volume: 107.7 cm3; (16)Surface Tension: 83.5 dyne/cm; (17)Density: 1.551 g/cm3; (18)Flash Point: 301.4 °C; (19)Enthalpy of Vaporization: 90.58 kJ/mol; (20)Boiling Point: 574.8 °C at 760 mmHg; (21)Vapour Pressure: 4.71E-14 mmHg at 25 °C.

Preparation of 2,4-Pyridinedicarboxylic acid: this chemical can be prepared by 2,4-Dimethyl-pyridine. This reaction needs reagents oxygen, Cu(NO3)2, H2O at temperature of 225-230 °C.

2,4-Pyridinedicarboxylic acid can be prepared by 2,4-Dimethyl-pyridine.

When you are dealing with this chemical, you should be very careful. This chemical is inflammation to the skin, eyes and respiratory system or other mucous membranes. Therefore, you should avoid contacting with skin and eyes. In case of contacting with eyes, you should rinse immediately with plenty of water and seek medical advice.

You can still convert the following datas into molecular structure:
(1) SMILES: O=C(O)c1nccc(C(=O)O)c1
(2) InChI: InChI=1S/C7H5NO4/c9-6(10)4-1-2-8-5(3-4)7(11)12/h1-3H,(H,9,10)(H,11,12)
(3) InChIKey: MJIVRKPEXXHNJT-UHFFFAOYSA-N

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