Product Name

  • Name

    1,4-Phenylenediacetic acid

  • EINECS 230-801-2
  • CAS No. 7325-46-4
  • Article Data21
  • CAS DataBase
  • Density 1.345 g/cm3
  • Solubility very soluble in water
  • Melting Point 248-252 °C(lit.)
  • Formula C10H10O4
  • Boiling Point 410.7 °C at 760 mmHg
  • Molecular Weight 194.187
  • Flash Point 216.4 °C
  • Transport Information
  • Appearance light yellow to beige powder
  • Safety 26-36-37/39
  • Risk Codes 36/37/38
  • Molecular Structure Molecular Structure of 7325-46-4 (1,4-Phenylenediacetic acid)
  • Hazard Symbols IrritantXi
  • Synonyms p-Phenylenediacetic acid;p-Benzenediaceticacid (6CI,7CI,8CI);1,4-Benzenediaceticacid;
  • PSA 74.60000
  • LogP 0.94080

Synthetic route

1,4-phenylenediacetonitrile
622-75-3

1,4-phenylenediacetonitrile

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

Conditions
ConditionsYield
With hydrogenchloride; acetic acid at 100℃; for 2h;90%
With hydrogenchloride; water at 100℃; for 12h;88%
With hydrogenchloride
carbon monoxide
201230-82-2

carbon monoxide

p-Xylylene dichloride
623-25-6

p-Xylylene dichloride

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

Conditions
ConditionsYield
Stage #1: carbon monoxide With C28H16N2O6Se In butan-1-ol under 750.075 Torr; for 2h; Reflux;
Stage #2: p-Xylylene dichloride With tetrabutylammomium bromide; sodium hydroxide In butan-1-ol at 50℃; under 750.075 Torr; for 24h;
90%
Stage #1: carbon monoxide With C28H22CoN4O6 In butan-1-ol at 60℃; under 760.051 Torr; for 2h; Glovebox; High pressure; Green chemistry;
Stage #2: p-Xylylene dichloride With tetra-(n-butyl)ammonium iodide; sodium hydroxide In butan-1-ol at 60℃; under 760.051 Torr; for 22h; Glovebox; High pressure; Green chemistry; regioselective reaction;
80%
1,4-bis(bromomethyl)benzene
623-24-5

1,4-bis(bromomethyl)benzene

carbon monoxide
201230-82-2

carbon monoxide

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

Conditions
ConditionsYield
With chloro(1,5-cyclooctadiene)rhodium(I) dimer; potassium iodide In formic acid at 90℃; under 760 Torr; for 18h; Carbonylation;89%
1,4-bis(2,2-dibromoethenyl)benzene
77295-67-1

1,4-bis(2,2-dibromoethenyl)benzene

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

Conditions
ConditionsYield
Stage #1: 1,4-bis(2,2-dibromoethenyl)benzene With n-butyllithium In tetrahydrofuran at 0℃; for 1.5h;
Stage #2: With 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane In tetrahydrofuran for 2h;
60%
diethyl 2,2'-(1,4-phenylene)diacetate
36076-26-3

diethyl 2,2'-(1,4-phenylene)diacetate

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

Conditions
ConditionsYield
With sodium hydroxide In ethanol; water for 9h; Heating;57%
carbon monoxide
201230-82-2

carbon monoxide

p-xylylene glycol
589-29-7

p-xylylene glycol

A

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

B

4-tolylacetic acid
622-47-9

4-tolylacetic acid

Conditions
ConditionsYield
With tetrakis(triphenylphosphine) palladium(0); hydrogen iodide In acetone at 90℃; under 68400 Torr; for 42h;A 48%
B 16 % Spectr.
carbon monoxide
201230-82-2

carbon monoxide

p-xylylene glycol
589-29-7

p-xylylene glycol

A

para-xylene
106-42-3

para-xylene

B

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

C

4-tolylacetic acid
622-47-9

4-tolylacetic acid

Conditions
ConditionsYield
With hydrogen iodide; tetrakis(triphenylphosphine) palladium(0) In acetone at 90℃; under 68400 Torr; for 42h; Carbonylation; reduction;A n/a
B 48%
C 16%
octane
111-65-9

octane

para-xylene
106-42-3

para-xylene

n-pentylsodium
1822-71-5

n-pentylsodium

A

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

B

4-tolylacetic acid
622-47-9

4-tolylacetic acid

C

hexanoic acid
142-62-1

hexanoic acid

Conditions
ConditionsYield
Behandlung des Reaktionsprodukts mit festem CO2;
4-acetyl-phenylacetic acid
7398-52-9

4-acetyl-phenylacetic acid

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

Conditions
ConditionsYield
With morpholine; sulfur Erwaermen des Reaktionsprodukts mit aethanol. Kalilauge;
ethyl 4-acetylphenylacetate
1528-42-3

ethyl 4-acetylphenylacetate

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

Conditions
ConditionsYield
With morpholine; sulfur Erwaermen des Reaktionsprodukts mit aethanol. Kalilauge;
para-xylene
106-42-3

para-xylene

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

Conditions
ConditionsYield
With octane; n-pentylsodium anschliessendes Behandeln mit festem Kohlendioxid;
p-phenylene-bis-thioacetic acid diamide

p-phenylene-bis-thioacetic acid diamide

alcoholic potash

alcoholic potash

A

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

B

hydrogen sulfide
7783-06-4

hydrogen sulfide

C

ammonia
7664-41-7

ammonia

p-Xylylene dichloride
623-25-6

p-Xylylene dichloride

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 87 percent / triethylene glycol / 1 h / 90 °C
2: 90 percent / conc. HCl; acetic acid / 2 h / 100 °C
View Scheme
Multi-step reaction with 2 steps
1: aq. ethanol / Heating
2: aq. H2SO4 / Heating
View Scheme
Ethyl 2-phenylethanoate
101-97-3

Ethyl 2-phenylethanoate

butylamine salts

butylamine salts

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 78 percent / SnCl4 / CH2Cl2 / 24 h / Ambient temperature
2: 86 percent / Raney nickel / ethanol / 4 h / Heating
3: 57 percent / sodium hydroxide / ethanol; H2O / 9 h / Heating
View Scheme
diethyl α-methylthio-1,4-benzenediacetate
105077-01-8

diethyl α-methylthio-1,4-benzenediacetate

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 86 percent / Raney nickel / ethanol / 4 h / Heating
2: 57 percent / sodium hydroxide / ethanol; H2O / 9 h / Heating
View Scheme
diethyl 2,2'-(1,4-phenylene)diacetate
36076-26-3

diethyl 2,2'-(1,4-phenylene)diacetate

A

2-(4-(2-ethoxy-2-oxoethyl)phenyl)acetic acid
113520-36-8

2-(4-(2-ethoxy-2-oxoethyl)phenyl)acetic acid

B

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

Conditions
ConditionsYield
With lithium hydroxide monohydrate; water In tetrahydrofuran; ethanol
C10H8O4(2-)*Zn(2+)*C10H8N2*CH4O

C10H8O4(2-)*Zn(2+)*C10H8N2*CH4O

A

4,4'-bipyridine
553-26-4

4,4'-bipyridine

B

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

Conditions
ConditionsYield
With sulfuric acid-d2 In dimethylsulfoxide-d6
1,4-diethynylbenzene
935-14-8

1,4-diethynylbenzene

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

Conditions
ConditionsYield
Stage #1: 1,4-diethynylbenzene With n-butyllithium In tetrahydrofuran at -78℃; for 1h;
Stage #2: With 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane In tetrahydrofuran for 2h;
Stage #3: With oxone In acetone at 50℃; for 12h;
Multi-step reaction with 2 steps
1.1: n-butyllithium / tetrahydrofuran; hexane / 1 h / -78 °C / Inert atmosphere
1.2: 2 h / -78 °C / Inert atmosphere
2.1: oxone||potassium monopersulfate triple salt; water / acetone / 12 h / 50 °C / Inert atmosphere
View Scheme
1,4-bis((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethynyl)benzene

1,4-bis((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethynyl)benzene

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

Conditions
ConditionsYield
With oxone||potassium monopersulfate triple salt; water In acetone at 50℃; for 12h; Inert atmosphere;689 mg
methanol
67-56-1

methanol

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

(4-methoxycarbonylmethylphenyl)acetic acid methyl ester
36076-25-2

(4-methoxycarbonylmethylphenyl)acetic acid methyl ester

Conditions
ConditionsYield
With sulfuric acid Reflux;100%
With sulfuric acid at 80℃; for 94h; Inert atmosphere;90%
With thionyl chloride for 4h; Reflux;85%
ethanol
64-17-5

ethanol

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

(4-methoxycarbonylmethylphenyl)acetic acid methyl ester
36076-25-2

(4-methoxycarbonylmethylphenyl)acetic acid methyl ester

Conditions
ConditionsYield
With sulfuric acid In water at 80℃; for 12h; Inert atmosphere;99%
N(1),N(2)-bis(t-butyloxycarbonyl)-1,2,4-butanetriamine
139024-81-0

N(1),N(2)-bis(t-butyloxycarbonyl)-1,2,4-butanetriamine

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

C38H64N6O10

C38H64N6O10

Conditions
ConditionsYield
With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine In acetonitrile at 0 - 20℃; Reflux;97%
1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

phenylenediacetic acid-2,2,2',2'-d4
104183-03-1

phenylenediacetic acid-2,2,2',2'-d4

Conditions
ConditionsYield
With potassium hydroxide; water-d2 at 160℃; for 28h;95%
1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

2,3-dihydro-1H-isoindole-5,6-dicarboxylic acid 5-{[2-(4-fluoro-phenyl)-ethyl]-amide} 6-(4-methyl-benzylamide)

2,3-dihydro-1H-isoindole-5,6-dicarboxylic acid 5-{[2-(4-fluoro-phenyl)-ethyl]-amide} 6-(4-methyl-benzylamide)

C62H58F2N6O6

C62H58F2N6O6

Conditions
ConditionsYield
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 25℃; for 12h;94%
1,2-bis(5-methylisoxazol-3-yl)hydrazine
2632-99-7

1,2-bis(5-methylisoxazol-3-yl)hydrazine

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

zinc(II) acetate dihydrate
5970-45-6

zinc(II) acetate dihydrate

[Zn(μ4-1,4-phenylenediacetate)(μ-4,4′-azobis(pyridine))0.5]n

[Zn(μ4-1,4-phenylenediacetate)(μ-4,4′-azobis(pyridine))0.5]n

Conditions
ConditionsYield
In water at 70 - 120℃; for 72.5h;93%
1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

2-[4-(2-hydroxyethyl)phenyl]ethan-1-ol
5140-03-4

2-[4-(2-hydroxyethyl)phenyl]ethan-1-ol

Conditions
ConditionsYield
With lithium aluminium tetrahydride In tetrahydrofuran Ambient temperature;92%
Stage #1: 1,4-phenylenediacetic acid With dimethyl sulfide borane In tetrahydrofuran for 18h;
Stage #2: With hydrogenchloride In tetrahydrofuran; water
87%
With dimethylsulfide borane complex In tetrahydrofuran at 0 - 20℃; for 24h; Inert atmosphere;81.8%
1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

4'-methoxy-N-(azulen-1-ylmethylene)aniline
854154-95-3

4'-methoxy-N-(azulen-1-ylmethylene)aniline

1,4-bis[(E)-2-(azulen-1-yl)vinyl]benzene

1,4-bis[(E)-2-(azulen-1-yl)vinyl]benzene

Conditions
ConditionsYield
for 10h; Heating;91%
pyrrolidine
123-75-1

pyrrolidine

trimethylsilyl cyanide
7677-24-9

trimethylsilyl cyanide

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

C20H26N4

C20H26N4

Conditions
ConditionsYield
Stage #1: pyrrolidine; 1,4-phenylenediacetic acid With (dimethoxy)methylsilane; molybdenum hexacarbonyl at 65℃;
Stage #2: trimethylsilyl cyanide In 2,2,2-trifluoroethanol at 20℃; for 1h; chemoselective reaction;
91%
ethanol
64-17-5

ethanol

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

diethyl 2,2'-(1,4-phenylene)diacetate
36076-26-3

diethyl 2,2'-(1,4-phenylene)diacetate

Conditions
ConditionsYield
With sulfuric acid for 15h; Reflux;90%
With sulfuric acid at 80℃;87%
With sulfuric acid for 18h; Heating;74%
acetyl chloride for 18h; Heating / reflux;
1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

1,4-benzenediacetaldehyde
39246-00-9

1,4-benzenediacetaldehyde

Conditions
ConditionsYield
With triethylsilane; tris(pentafluorophenyl)borate In benzene at 23℃; for 6h; Schlenk technique; Inert atmosphere;90%
Multi-step reaction with 3 steps
1: 74 percent / aq. H2SO4 / 18 h / Heating
2: 84 percent / LiAlH4 / diethyl ether / 3 h / Heating
3: 62 percent / Dess-Matin periodinane / CH2Cl2 / 4 h / 20 °C
View Scheme
europium(III) nitrate hexahydrate

europium(III) nitrate hexahydrate

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

[(europium(III))2(1,4-phenylenediacetate)3(H2O)] dihydrate

[(europium(III))2(1,4-phenylenediacetate)3(H2O)] dihydrate

Conditions
ConditionsYield
In N,N-dimethyl acetamide; water High Pressure; mixt. of Eu(NO3)3*6H2O (0.4 mmol), H2pda (0.6 mmol), H2O and dimethylacetamide heated in Teflon-lined autoclave at 105°C for 2 d, cooled slowly to room temp.; elem. anal.;90%
yttrium(lll) nitrate hexahydrate

yttrium(lll) nitrate hexahydrate

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

[Y2(1,4-phenylenediacetate)3(H2O)1]*2H2O

[Y2(1,4-phenylenediacetate)3(H2O)1]*2H2O

Conditions
ConditionsYield
In ethanol; water at 180℃; for 1.16667h;90%
1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

(3S,4S)-N3,N4-bis(((1S,2R)-2-phenylcyclopropyl)carbamoyl)pyrrolidine-3,4-dicarboxamide hydrochloride

(3S,4S)-N3,N4-bis(((1S,2R)-2-phenylcyclopropyl)carbamoyl)pyrrolidine-3,4-dicarboxamide hydrochloride

(3S,3’S,4S,4’S)-1,1’-((1,4-phenylene)diacetyl)-bis(N3,N4-bis((1S,2R)-2-phenylcyclopropyl)pyrrolidine-3,4-dicarboxamide)

(3S,3’S,4S,4’S)-1,1’-((1,4-phenylene)diacetyl)-bis(N3,N4-bis((1S,2R)-2-phenylcyclopropyl)pyrrolidine-3,4-dicarboxamide)

Conditions
ConditionsYield
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 23℃; for 18h;89%
1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

phenylglyoxylic acid potassium salt
63468-90-6

phenylglyoxylic acid potassium salt

1,4-Phenylene bis(phenylmaleic anhydride)
104595-14-4

1,4-Phenylene bis(phenylmaleic anhydride)

Conditions
ConditionsYield
With acetic anhydride for 1h; Heating;88%
nickel(II) nitrate hexahydrate

nickel(II) nitrate hexahydrate

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

1,3-bis(1H-imidazol-4-yl)benzene
794485-43-1

1,3-bis(1H-imidazol-4-yl)benzene

water
7732-18-5

water

C12H10N4*C10H8O4(2-)*H2O*Ni(2+)

C12H10N4*C10H8O4(2-)*H2O*Ni(2+)

Conditions
ConditionsYield
With sodium hydroxide at 120℃; for 72h; Sealed tube; Autoclave;88%
1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

Diphenylphosphine oxide
4559-70-0

Diphenylphosphine oxide

(1,4-phenylenebis(methylene))bis(diphenylphosphine oxide)
38661-56-2

(1,4-phenylenebis(methylene))bis(diphenylphosphine oxide)

Conditions
ConditionsYield
With sodium persulfate; silver carbonate In acetonitrile at 80℃;88%
1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

1,4-benzenediacetyl dichloride
21062-19-1

1,4-benzenediacetyl dichloride

Conditions
ConditionsYield
With Vilsmeier reagent In toluene at 35 - 40℃; for 0.25h;87%
With thionyl chloride
With phosphorus pentachloride
1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

L-Leu-L-Pro-OMe
72087-28-6

L-Leu-L-Pro-OMe

1,4-phenylenedi(acetyl-L-leucyl-L-proline methyl ester)
668479-44-5

1,4-phenylenedi(acetyl-L-leucyl-L-proline methyl ester)

Conditions
ConditionsYield
Stage #1: 1,4-phenylenediacetic acid With diisopropyl-carbodiimide In dichloromethane for 0.75h;
Stage #2: L-Leu-L-Pro-OMe In dichloromethane for 16h;
86%
gadolinium(III) nitrate hexahydrate

gadolinium(III) nitrate hexahydrate

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

[(gadolinium(III))2(1,4-phenylenediacetate)3(H2O)] dihydrate

[(gadolinium(III))2(1,4-phenylenediacetate)3(H2O)] dihydrate

Conditions
ConditionsYield
In N,N-dimethyl acetamide; water High Pressure; mixt. of Gd(NO3)3*6H2O (0.4 mmol), H2pda (0.6 mmol), H2O and dimethylacetamide heated in Teflon-lined autoclave at 105°C for 2 d, cooled slowly to room temp.; elem. anal.;86%
1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

zinc(II) nitrate hexahydrate

zinc(II) nitrate hexahydrate

4,4'-di(4-pyridyl)stilbene

4,4'-di(4-pyridyl)stilbene

[Zn(1,4-pda)(4,4'-di(4-pyridyl)stilbene)]n

[Zn(1,4-pda)(4,4'-di(4-pyridyl)stilbene)]n

Conditions
ConditionsYield
In water for 72h; Autoclave; High pressure;86%
cobalt(II) chloride hexahydrate

cobalt(II) chloride hexahydrate

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

water
7732-18-5

water

[Co(1,4-phenylenediacetate)(H2O)2]

[Co(1,4-phenylenediacetate)(H2O)2]

Conditions
ConditionsYield
With sodium carbonate In water High Pressure; addn. of aq. soln. of sodium carbonate to aq. soln. of carbon compd., addn. of aq. soln. of cobalt compd. at room temp., sealing in stainless steel reactor, heating at 120°C for 48 h; cooling, isolation of crystals by hand, washing with water, drying over filter paper, elem. anal.;85%
yttrium(lll) nitrate hexahydrate

yttrium(lll) nitrate hexahydrate

europium(III) nitrate hexahydrate

europium(III) nitrate hexahydrate

1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

[Y1.8Eu0.2(1,4-phenylenediacetate)3(H2O)1]*2H2O

[Y1.8Eu0.2(1,4-phenylenediacetate)3(H2O)1]*2H2O

Conditions
ConditionsYield
In ethanol; water at 180℃; for 1.16667h; Milling;85%
1,4-phenylenediacetic acid
7325-46-4

1,4-phenylenediacetic acid

Benzoylformic acid
611-73-4

Benzoylformic acid

1,4-Phenylene bis(phenylmaleic anhydride)
104595-14-4

1,4-Phenylene bis(phenylmaleic anhydride)

Conditions
ConditionsYield
With acetic anhydride; sodium hydride Reflux;85%

1,4-PHENYLENEDIACETIC ACID Chemical Properties

The MF of 1,4-PHENYLENEDIACETIC ACID(7325-46-4): C10H10O4
The MW of 1,4-PHENYLENEDIACETIC ACID(7325-46-4): 194.18
EINECS: 230-801-2
mp: 248-252 °C(lit.)
Density: 1.345 g/cm3 
Flash Point: 216.4 °C 
Boiling Point: 410.7 °C at 760 mmHg 
Index of Refraction: 1.586
Categories: Aromatic Phenylacetic Acids and Derivatives;C10;Carbonyl Compounds;Carboxylic Acids
Synonyms: BENZENE-1,4-DIACETIC ACID;1,4-PHENYLENEDIACETIC ACID;P-BENZENEDIACETIC ACID;P-PHENYLENEDIACETIC ACID;RARECHEM AL BO 0138;1,4-Benzenediacetic acid;4-Phenylenediacetic acid;1,4-Phenylenebis(acetic acid)
The Structure of 1,4-PHENYLENEDIACETIC ACID(7325-46-4):

1,4-PHENYLENEDIACETIC ACID Safety Profile

Hazard Codes: Xi
Risk Statements: 36/37/38
Risk Statements: 36/37/38
36/37/38:  Irritating to eyes, respiratory system and skin 
Safety Statements: 26-36-37/39
26:  In case of contact with eyes, rinse immediately with plenty of water and seek medical advice 
36:  Wear suitable protective clothing 
37/39:  Wear suitable gloves and eye/face protection 
WGK Germany: 3
TSCA: T
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