METHOXYACETIC ACID supplier

Name
Methoxyacetic acid
EINECS 210-894-6
CAS No. 625-45-6
Article Data50
CAS DataBase
Density 1.139 g/cm³
Solubility freely soluble in water
Melting Point 7-9 °C(lit.)
Formula C₃H₆O₃
Boiling Point 201 °C at 760 mmHg
Molecular Weight 90.0788
Flash Point 94 °C
Transport Information UN 3265 8/PG 2
Appearance Clear colourless to very slightly yellow liquid
Safety 53-45
Risk Codes 60-61-22-34
Molecular Structure
Hazard Symbols T
Synonyms 2-Methoxyacetic acid;Methoxyacetic acid;Methoxyethanoic acid;Aceticacid, methoxy- (6CI,7CI,8CI,9CI);NSC 7300;
PSA 46.53000
LogP -0.28260

Synthetic route

: 109-86-4
2-methoxy-ethanol

: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
Stage #1: 2-methoxy-ethanol With (6-di-tert-butylphosphinomethyl-2,2’-bipyridyl)Ru(CO)HCl; water; sodium hydroxide for 18h; Inert atmosphere; Reflux; Stage #2: Acidic conditions;	73%
Stage #1: 2-methoxy-ethanol With C12H14ClN2Ru(1+)*F6P(1-); potassium hydroxide In toluene at 110℃; for 6h; Inert atmosphere; Stage #2: With hydrogenchloride In water	52%
Stage #1: 2-methoxy-ethanol With [RuCl2(p-cymene)(iPr2-imy)]; tricyclohexylphosphine tetrafluoroborate; potassium hydroxide In toluene for 18h; Schlenk technique; Inert atmosphere; Reflux; Stage #2: With hydrogenchloride In water pH=1;	51%

: 124-41-4
sodium methylate

: 79-11-8
chloroacetic acid

: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
In methanol	65%
With methanol

: 10312-83-1
methoxyacetaldehyde

: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
With oxygen; cobalt(II) acetate at 50 - 70℃;
With air; manganese(II) acetate at 50 - 70℃;
With air; cobalt(II) acetate at 50 - 70℃;
With oxygen; manganese(II) acetate at 50 - 70℃;

: 107-16-4
glycolonitrile

: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
With hydrogenchloride

: 67-56-1
methanol

: 79-11-8
chloroacetic acid

: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
at 200℃;
With sodium methylate Reflux;

: 16356-02-8
1,4-dimethoxy-2-butyne

: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
With potassium permanganate

: 20605-41-8
methoxyacetic acid hydrazide

: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
With sulfuric acid at 70 - 80℃; Thermodynamic data;

: 124-38-9
carbon dioxide

: 107-30-2
chloromethyl methyl ether

: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
(i) Li, dimethoxymethane, (ii) /BRN= 1900390/; Multistep reaction;

: 67-56-1
methanol

: 143659-33-0
1-Naphthylmethyl methoxyacetate

A: 91909-27-2
2-(1-naphthyl)ethyl methyl ether

B: 5903-23-1
1-(methoxymethyl)naphthalene

C: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
Irradiation;	A 10 % Chromat. B 89 % Chromat. C n/a
Rate constant; Quantum yield; Irradiation; rate of decarboxylation k(CO2);	A 10 % Chromat. B 89 % Chromat. C n/a

...Expand

: 6290-49-9
methyl methoxyacetate

: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
In sodium hydroxide at 25℃; Thermodynamic data;

: 530-55-2
2,6-dimethoxy-p-quinone

A: 2509-15-1
methoxy-maleic acid

B: 15233-65-5
2,6-dimethoxy-1,4-hydroquinone

C: 144-62-7
oxalic acid

D: 64-19-7
acetic acid

E: 77292-35-4
2,6-dimethoxy-3-hydroxy-p-benzoquinone

F: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
With sodium hydroxide; sodium silicate; diethylenetriaminopentaacetic acid; dihydrogen peroxide In water at 25℃; for 1h; Mechanism; pH 9.0;

...Expand

: 34359-77-8
trimethyl orthoester of methoxyacetic acid

: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
In hydrogenchloride at 25℃; Thermodynamic data;

: 133604-76-9
3,5-dimethylphenyl methoxyacetate

A: 625-45-6
2-methoxyacetic acid

B: 108-68-9
3,5-Dimethylphenol

Conditions

Conditions	Yield
With sodium hydroxide; water In ethanol at 30℃; Rate constant;

: 19500-95-9
Methoxyacetic anhydride

: 64-19-7
acetic acid

A: 136684-61-2
acetic 2-methoxyacetic anhydride

B: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
at 80 - 90℃; Equilibrium constant;

...Expand

: 64-19-7
acetic acid

: 136684-61-2
acetic 2-methoxyacetic anhydride

A: 108-24-7
acetic anhydride

B: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
at 80 - 90℃; Equilibrium constant;

...Expand

: Phenylamine; compound with methoxy-acetic acid

A: 62-53-3
aniline

B: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
In hexane at 25℃; Equilibrium constant; the influence of the acid concentration;

: 111-96-6
diethylene glycol dimethyl ether

: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
With hydrogenchloride; sodium hypochlorite

: 625-48-9
2-nitro-1-ethanol

: 20758-58-1
2-methoxyacetate

A: 188819-30-9
C2H4NO3(1-)

B: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
In water at 25℃; Rate constant;

...Expand

: 1794-90-7
2-nitropropane-1,3-diol

: 20758-58-1
2-methoxyacetate

A: 184582-82-9
C3H6NO4(1-)

B: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
In water at 25℃; Rate constant;

...Expand

: 67-56-1
methanol

: 3926-62-3
sodium monochloroacetic acid

: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
With sodium hydride

: 54620-66-5
5-methoxy-2-methoxymethyl-4H-pyran-4-one

aq. barium hydroxide solution: aq. barium hydroxide solution

A: 64-18-6
formic acid

B: 5878-19-3
Methoxyacetone

C: 625-45-6
2-methoxyacetic acid

...Expand

: 54620-66-5
5-methoxy-2-methoxymethyl-4H-pyran-4-one

: 7732-18-5
water

barium hydroxide: barium hydroxide

A: 64-18-6
formic acid

B: 5878-19-3
Methoxyacetone

C: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
at 100℃;

...Expand

: 115-10-6
Dimethyl ether

: 124-38-9
carbon dioxide

: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
With phosphoric acid at 300 - 400℃; under 73550.8 - 183877 Torr;

6-methyl-galactose: 6-methyl-galactose

: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
With water; silver(l) oxide das Silbersalz entsteht;

: 16356-02-8
1,4-dimethoxy-2-butyne

KMnO4: KMnO4

: 625-45-6
2-methoxyacetic acid

: 5-methoxy-pent-3-enenitrile

alkaline KMnO4: alkaline KMnO4

: 625-45-6
2-methoxyacetic acid

: 115-10-6
Dimethyl ether

: 124-38-9
carbon dioxide

: 86119-84-8, 7664-38-2
phosphoric acid

coal: coal

: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
at 300 - 400℃; under 73550.8 - 183877 Torr;

...Expand

: 10312-83-1
methoxyacetaldehyde

air: air

cobalt acetate: cobalt acetate

: 625-45-6
2-methoxyacetic acid

Conditions

Conditions	Yield
at 50 - 70℃;

...Expand

: 22805-71-6
(E)-1,4-dimethoxy-2-butene

KMnO4: KMnO4

: 625-45-6
2-methoxyacetic acid

: 709666-19-3
3,4-diamino-5-methyl-phenol

: 625-45-6
2-methoxyacetic acid

: 1231749-90-8
2-(methoxymethyl)-4-methyl-1H-benzo[d]imidazol-6-ol

Conditions

Conditions	Yield
at 120℃; for 1h;	100%

: 879089-16-4, 155065-88-6
[Cu2(OAc)4(H2O)2]

: 625-45-6
2-methoxyacetic acid

: Copper(II) 2-methoxyacetate

Conditions

Conditions	Yield
In toluene at 111℃; for 5h;	100%

: 133217-42-2
thiocarbonic acid S-ethyl ester O-iodomethyl ester

: 625-45-6
2-methoxyacetic acid

: C7H12O5S

Conditions

Conditions	Yield
Stage #1: 2-methoxyacetic acid With tetra(n-butyl)ammonium hydrogensulfate; sodium hydrogencarbonate In dichloromethane; water at 20℃; for 1h; Inert atmosphere; Stage #2: thiocarbonic acid S-ethyl ester O-iodomethyl ester In dichloromethane; water at 20℃; for 3h; Inert atmosphere;	100%

: 111-87-5
octanol

: 625-45-6
2-methoxyacetic acid

: 29267-10-5
1-octyl methoxyacetate

Conditions

Conditions	Yield
With dimesitylammonium pentafluorobenzenesulfonate In n-heptane at 80℃; for 1h;	99%
With sulfonated polypyrene In n-heptane at 110℃; for 1h;	95%
fluorous ammonium triflate In toluene at 80℃; for 1h;	94%
With high p-toluenesulfonate content diphenylamine and terephthalaldehyde resin In neat (no solvent) at 110℃; for 2h;	88%
With ytterbium(III) triflate Yield given;

: 625-45-6
2-methoxyacetic acid

: 1,5-dimethyl-2-cyclohexen-1-ol

: Methoxy-acetic acid (1R,5S)-1,5-dimethyl-cyclohex-2-enyl ester

Conditions

Conditions	Yield
With dmap; dicyclohexyl-carbodiimide In dichloromethane Ambient temperature;	99%

: 186581-53-3, 908094-01-9
diazomethane

: 625-45-6
2-methoxyacetic acid

: 320776-89-4
(1S)-1-(trifluoromethyl)-(2E)-nonenyl methanesulfonate

: (E)-(2S,3R)-2-Methoxy-3-trifluoromethyl-undec-4-enoic acid methyl ester

Conditions

Conditions	Yield
Multistep reaction;	99%

...Expand

: 150-76-5
4-methoxy-phenol

: 625-45-6
2-methoxyacetic acid

: p-methoxyphenyl methoxyacetate

Conditions

Conditions	Yield
With dimesitylammonium pentafluorobenzenesulfonate In n-heptane at 115℃; for 24h;	99%
dimesitylammonium pentafluorobenzenesulfonate In n-heptane at 115℃; for 24h; Product distribution / selectivity;	99%
With toluene-4-sulfonic acid at 80℃; for 26h;	39%

: 75-36-5
acetyl chloride

: 625-45-6
2-methoxyacetic acid

: 136684-61-2
acetic 2-methoxyacetic anhydride

Conditions

Conditions	Yield
Stage #1: 2-methoxyacetic acid With triethylamine In dichloromethane at 20℃; for 1h; Stage #2: acetyl chloride In dichloromethane	99%

: 25944-64-3
diethyl (1-phenylethenyl)phosphonate

: 625-45-6
2-methoxyacetic acid

: diethyl (3-methoxy-1-phenylpropyl)phosphonate

Conditions

Conditions	Yield
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate; caesium carbonate In dimethyl sulfoxide at 20℃; for 24h; Giese Free Radical Synthesis; Schlenk technique; Inert atmosphere; Irradiation;	99%

: N,N-diethyl-N-(2-methoxyethyl)-N-methylammonium methyl carbonate

: 625-45-6
2-methoxyacetic acid

: N,N-diethyl-N-(2-methoxyethyl)-N-methylammonium methoxyacetate

Conditions

Conditions	Yield
In methanol at 20℃; for 1h;	99%

: 105376-04-3, 113214-71-4, 138661-53-7
ethyl 2,3,4,6-tetra-O-benzoyl-1-thio-β-D-galactopyranoside

: 625-45-6
2-methoxyacetic acid

: C37H32O12

Conditions

Conditions	Yield
With N-iodo-succinimide In diethyl ether; 1,2-dichloro-ethane at 20℃; for 0.333333h;	98%

: 91001-09-1
(E,Z)-hepta-2,5-dien-4-ol

: 625-45-6
2-methoxyacetic acid

: Methoxy-acetic acid (Z)-((E)-1-propenyl)-but-2-enyl ester

Conditions

Conditions	Yield
With dmap; dicyclohexyl-carbodiimide In dichloromethane Ambient temperature;	98%

: 52755-38-1
(Z)-1-phenyl-but-2-en-1-ol

: 625-45-6
2-methoxyacetic acid

: Methoxy-acetic acid (Z)-1-phenyl-but-2-enyl ester

Conditions

Conditions	Yield
With dmap; dicyclohexyl-carbodiimide In dichloromethane Ambient temperature;	98%

: 72777-19-6
(3S,8R,9S,10R,13S,14S,16R)-17-Eth-(E)-ylidene-10,13-dimethyl-3-(tetrahydro-pyran-2-yloxy)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-16-ol

: 625-45-6
2-methoxyacetic acid

: Methoxy-acetic acid (3S,8R,9S,10R,13S,14S,16R)-17-eth-(E)-ylidene-10,13-dimethyl-3-(tetrahydro-pyran-2-yloxy)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-16-yl ester

Conditions

Conditions	Yield
With dmap; dicyclohexyl-carbodiimide In dichloromethane Ambient temperature;	98%

: 529-02-2, 18649-91-7, 22472-79-3, 22472-80-6, 29910-20-1, 118760-35-3
cis-pulegol

: 625-45-6
2-methoxyacetic acid

: Methoxy-acetic acid (1S,5S)-2-isopropylidene-5-methyl-cyclohexyl ester

Conditions

Conditions	Yield
With dmap; dicyclohexyl-carbodiimide In dichloromethane Ambient temperature;	98%

: 625-45-6
2-methoxyacetic acid

: 188637-63-0
(6-bromopyridin-2-yl)methanamine

: 914947-25-4
C9H11BrN2O2

Conditions

Conditions	Yield
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide	98%

: 3-bromo-4-fluoro-benzylamine hydrochloride

: 625-45-6
2-methoxyacetic acid

: N-[(3-bromo-4-fluorophenyl)methyl]-2-methoxyacetamide

Conditions

Conditions	Yield
With 4-methyl-morpholine; 1-hydroxybenzotriazol-hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; for 16h; Inert atmosphere;	98%

: (R)-5-(2-methyl-4-phenoxyphenyl)-4-oxo-N-(piperidin-3-yl)-4,5-dihydro-3H-1-thia-3,5,8-triazaacenaphthylene-2-carboxamide

: 625-45-6
2-methoxyacetic acid

: (R)-N-(1-(2-methoxyacetyl)piperidin-3-yl)-5-(2-methyl-4-phenoxyphenyl)-4-oxo-4,5-dihydro-3H-1-thia-3,5,8-triazaacenaphthylene-2-carboxamide

Conditions

Conditions	Yield
With triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 20℃; for 3h; Reagent/catalyst;	98%
With N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 20℃; Inert atmosphere;	63%

: 2999-46-4
Ethyl isocyanoacetate

: 625-45-6
2-methoxyacetic acid

: ethyl 5-(methoxymethyl)oxazole-4-carboxylate

Conditions

Conditions	Yield
Stage #1: 2-methoxyacetic acid With 1,1'-carbonyldiimidazole In tetrahydrofuran at 55℃; for 1h; Stage #2: Ethyl isocyanoacetate With 1,8-diazabicyclo[5.4.0]undec-7-ene In tetrahydrofuran at 0 - 20℃; for 12h;	98%

: 71-23-8
propan-1-ol

: 625-45-6
2-methoxyacetic acid

: 17640-20-9
propyl 2-methoxyacetate

Conditions

Conditions	Yield
diphenyltin(IV) dichloride for 2h; Heating;	97%

: 625-45-6
2-methoxyacetic acid

: (E)-Non-2-en-5-yn-4-ol

: Methoxy-acetic acid ((E)-1-propenyl)-hex-2-ynyl ester

Conditions

Conditions	Yield
With dmap; dicyclohexyl-carbodiimide In dichloromethane Ambient temperature;	97%

: 2325-10-2
(S,S)-hydrobenzoin

: 625-45-6
2-methoxyacetic acid

: 1105044-26-5
(1S,2S)-1,2-diphenylethane-1,2-diyl bis(2-methoxyacetate)

Conditions

Conditions	Yield
With dmap; dicyclohexyl-carbodiimide In dichloromethane for 24h; Inert atmosphere;	97%

: 4-(trans-2,3-dihydro-2-hydroxy-1-indenyloxy)-6-(N,N-dimethylaminocarbonyl)-1,2-dimethyl-1H-benzimidazole

: 625-45-6
2-methoxyacetic acid

: 4-[trans-2,3-dihydro-2-(methoxymethylcarbonyloxy)-1-indenyloxy]-6-(N,N-dimethylamincarbonyl)-1,2-dimethyl-1H-benzimidazole

Conditions

Conditions	Yield
Stage #1: 2-methoxyacetic acid With 1,1'-carbonyldiimidazole In tetrahydrofuran for 0.25h; Stage #2: 4-(trans-2,3-dihydro-2-hydroxy-1-indenyloxy)-6-(N,N-dimethylaminocarbonyl)-1,2-dimethyl-1H-benzimidazole With 1,8-diazabicyclo[5.4.0]undec-7-ene In tetrahydrofuran for 1h;	97%

: (-)-englerin B

: 625-45-6
2-methoxyacetic acid

: C27H36O6

Conditions

Conditions	Yield
With dmap; 2,4,6-trichlorobenzoyl chloride; triethylamine In toluene at 20℃; Yamaguchi esterification; Inert atmosphere;	97%
With dmap; 2,4,6-trichlorobenzoyl chloride; triethylamine In toluene at 0 - 20℃; Inert atmosphere;

: 952-23-8
proflavine hydrochloride

: 625-45-6
2-methoxyacetic acid

: 3,6-(methoxyethylamino)acridine

Conditions

Conditions	Yield
With sodium tetrahydroborate for 72h; Inert atmosphere;	97%

: 64-19-7
acetic acid

: 625-45-6
2-methoxyacetic acid

: 320776-73-6
1-(trifluoromethyl)-(2E)-nonenyl methanesulfonate

: 1-(3,3,3-trifluoro-(1E)-propenyl)heptyl methoxyacetate

Conditions

Conditions	Yield
With triethylamine; tetrakis(triphenylphosphine) palladium(0) In tetrahydrofuran at 0℃; Substitution;	96%

...Expand

: 625-45-6
2-methoxyacetic acid

: 320776-73-6
1-(trifluoromethyl)-(2E)-nonenyl methanesulfonate

: 1-(3,3,3-trifluoro-(1E)-propenyl)heptyl methoxyacetate

Conditions

Conditions	Yield
Stage #1: 1-(trifluoromethyl)-(2E)-nonenyl methanesulfonate With tetrakis(triphenylphosphine) palladium(0) In tetrahydrofuran at 0℃; for 0.166667h; Stage #2: 2-methoxyacetic acid With triethylamine In tetrahydrofuran at 0℃; for 3h; Further stages.;	96%

: 95-14-7
1,2,3-Benzotriazole

: 625-45-6
2-methoxyacetic acid

: 1-(1H-1,2,3-benzotriazol-1-yl)-2-methoxy-1-ethanone

Conditions

Conditions	Yield
With thionyl chloride In dichloromethane at 25℃; for 2h;	96%
With thionyl chloride In dichloromethane at 20℃; for 2h;

: copper(II) choride dihydrate

: 7732-18-5
water

: 625-45-6
2-methoxyacetic acid

: 15660-52-3, 22239-89-0, 38426-73-2
trans-diaquabis(methoxyacetato)copper(II)

Conditions

Conditions	Yield
In methanol; water soln. of acid in CH3OH added to stirred soln. of CuCl2 in H2O; soln. filtered, washed with H2O, CH3OH, stand in air for 4 d.; elemn. anal.;	96%

...Expand

: 91-01-0
1,1-Diphenylmethanol

: 625-45-6
2-methoxyacetic acid

: 1533457-98-5
benzhydryl 2-methoxyacetate

Conditions

Conditions	Yield
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 12h;	96%

METHOXYACETIC ACID Chemical Properties

Product Name: Methoxyacetic acid
The MF of Methoxyacetic acid(625-45-6) is C₃H₆O₃.

The MW of Methoxyacetic acid(625-45-6) is 90.08.
Synonyms: 2-methoxyacetic;CH3OCH2COOH;Glycollicacid,methylether;methoxy-aceticaci;Methoxyethanoic acid;Methylglycolicacid;2-Methoxyacetic acid
Product Categories: Heterocyclic Compounds;C1 to C5;Carbonyl CompoundsMol File: 625-45-6.mol
EINECS: 210-894-6
Surface Tension: 35.5 dyne/cm
Density: 1.139 g/ml
Flash Point: 94 °C
MP: 7-9 °C(lit.)
Enthalpy of Vaporization: 48.19 kJ/mol
Boiling Point: 201 °C at 760 mmHg
Vapour Pressure: 0.131 mmHg at 25°C
Water Solubility: freely soluble
Sensitive: Hygroscopic
BRN: 635800
CAS DataBase Reference: 625-45-6(CAS DataBase Reference)
NIST Chemistry Reference: 625-45-6(NIST)
EPA Substance Registry System: 625-45-6(EPA Substance)

METHOXYACETIC ACID Toxicity Data With Reference

1.		dni-mus:emb25 mmol/L		TOLED5 Toxicology Letters. 45 (1989),111.
2.		orl-rat LDLo:2 g/kg		FAATDF Fundamental and Applied Toxicology. 2 (1982),158.

METHOXYACETIC ACID Consensus Reports

Reported in EPA TSCA Inventory.

METHOXYACETIC ACID Safety Profile

Moderately toxic by ingestion. An experimental teratogen. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes.
Safety information of Methoxyacetic acid(625-45-6):
Hazard Codes:

T
Risk Statements: 60-61-22-34
R60:May impair fertility ;
R61:May cause harm to the unborn child ;
R22:Harmful if swallowed ;
R34:Causes burns ;
Safety Statements: 53-45
S53:May cause long-term adverse effects in the aquatic environment ;
S45:May cause cancer ;
RIDADR: UN 3265 8/PG 2
WGK Germany: 1
RTECS: AI8650000
F: 10-21
HazardClass: 8
PackingGroup: II
HS Code: 29189090

METHOXYACETIC ACID Standards and Recommendations

DFG MAK: 5 ppm

METHOXYACETIC ACID Specification

The Methoxyacetic acid(625-45-6) is stable and soluble in water but incompatible with alkalis and metals.Hazardous decomposition products are carbon monoxide, carbon dioxide.

Product Name

Methoxyacetic acid

Synthetic route

METHOXYACETIC ACID Chemical Properties

METHOXYACETIC ACID Toxicity Data With Reference

METHOXYACETIC ACID Consensus Reports

METHOXYACETIC ACID Safety Profile

METHOXYACETIC ACID Standards and Recommendations

METHOXYACETIC ACID Specification

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