Product Name

  • Name

    Methoxyammonium chloride

  • EINECS 209-798-7
  • CAS No. 593-56-6
  • Article Data33
  • CAS DataBase
  • Density 0.854 g/cm3
  • Solubility soluble in water
  • Melting Point 151-154 °C(lit.)
  • Formula CH5NO.HCl
  • Boiling Point 49.5 °C at 760 mmHg
  • Molecular Weight 83.5177
  • Flash Point 18.2 °C
  • Transport Information UN 3265 8/PG 2
  • Appearance White to very faintly yellow crystalline powder
  • Safety 3-24-26-36/37/39-45-61-24/25-27
  • Risk Codes 34-36/37/38-50-43-20/21/22
  • Molecular Structure Molecular Structure of 593-56-6 (Methoxyammonium chloride)
  • Hazard Symbols CorrosiveC,IrritantXi,DangerousN
  • Synonyms Hydroxylamine,O-methyl-, hydrochloride (8CI,9CI);(Aminooxy)methane hydrochloride;Hydroxylamine methyl ether hydrochloride;Methoxyammonium chloride;N-Methoxylaminehydrochloride;O-Methoxyamine hydrochloride;O-Methylhydroxyaminehydrochloride;O-Methylhydroxylamine hydrochloride;
  • PSA 35.25000
  • LogP 1.00880

Synthetic route

N-methoxyphthalimide
1914-20-1

N-methoxyphthalimide

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

Conditions
ConditionsYield
Stage #1: N-methoxyphthalimide With methylhydrazine In dichloromethane at 0 - 20℃; for 2h;
Stage #2: With hydrogenchloride In 1,4-dioxane at 0℃;
90%
With hydrogenchloride for 0.5h; Hydrolysis; Heating;
With methylhydrazine In dichloromethane
Stage #1: N-methoxyphthalimide With hydrogenchloride; acetic acid In water for 1.5h; Reflux; Inert atmosphere;
Stage #2: With hydrogenchloride at 0 - 20℃; for 1h; Inert atmosphere;
N-methoxyacetamide
5806-90-6

N-methoxyacetamide

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

Conditions
ConditionsYield
With hydrogenchloride In ethanol; water at 65℃;69.3%
With hydrogenchloride In ethanol; water at 65℃;69.3%
benzyl bromide
100-39-0

benzyl bromide

6-chloropurine
87-42-3

6-chloropurine

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

Conditions
ConditionsYield
With potassium carbonate In dimethyl sulfoxide at 25℃; for 10h;48%
N-Methoxy-acetimidic acid ethyl ester

N-Methoxy-acetimidic acid ethyl ester

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

Conditions
ConditionsYield
With hydrogenchloride for 0.25h; Heating;
N-methoxybenzamide
2446-51-7

N-methoxybenzamide

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

Conditions
ConditionsYield
With hydrogenchloride In ethanol for 0.25h; Hydrolysis; Heating;
hydrogenchloride
7647-01-0

hydrogenchloride

(MeON=C(Me)-CMe=NOMe)
29144-51-2

(MeON=C(Me)-CMe=NOMe)

A

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

B

dimethylglyoxal
431-03-8

dimethylglyoxal

ethylbenzhydroximic acid methyl ester

ethylbenzhydroximic acid methyl ester

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

Conditions
ConditionsYield
With hydrogenchloride
methyl ether of benzaldoxime

methyl ether of benzaldoxime

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

Conditions
ConditionsYield
With hydrogenchloride
N-methoxysuccinimide
5904-50-7

N-methoxysuccinimide

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

Conditions
ConditionsYield
With hydrogenchloride
O-Methylhydroxylamin
67-62-9

O-Methylhydroxylamin

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

Conditions
ConditionsYield
With hydrogenchloride In water
With hydrogenchloride In ethanol
With hydrogenchloride30.2 g
With hydrogenchloride
With hydrogenchloride In water at 0 - 20℃; for 1h;
hydrogenchloride
7647-01-0

hydrogenchloride

(CH3O)H2N*BH3
91572-26-8

(CH3O)H2N*BH3

water
7732-18-5

water

A

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

B

boric acid
11113-50-1

boric acid

Conditions
ConditionsYield
In hydrogenchloride acidic hydrolysis;;
N-phenylacetyl-O-methylhydroxylamine
112403-78-8

N-phenylacetyl-O-methylhydroxylamine

A

phenylacetic acid
103-82-2

phenylacetic acid

B

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

Conditions
ConditionsYield
With Escherichia coli penicillin acylase; potassium chloride; water at 24.84℃; Equilibrium constant; Enzymatic reaction;
dimethyl sulfate
77-78-1

dimethyl sulfate

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

Conditions
ConditionsYield
With hydrogenchloride; sodium meta bi sulfate; sulfur dioxide; sodium nitrite In water at 100℃; for 3h; pH=4; Alkaline conditions;
(butan-2-ylidene)(methoxy)amine
27685-12-7

(butan-2-ylidene)(methoxy)amine

A

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

B

butanone
78-93-3

butanone

Conditions
ConditionsYield
With hydrogenchloride at 120℃; for 2.33333h; Temperature; Overall yield = 91 percent;
6-phenyl-hex-5-en-2-one
69371-59-1

6-phenyl-hex-5-en-2-one

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

N-Methoxy-1-phenyl-1-hexen-5-one oxime
134025-31-3

N-Methoxy-1-phenyl-1-hexen-5-one oxime

Conditions
ConditionsYield
With sodium acetate In water Heating;100%
N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

4-methoxy-benzaldehyde
123-11-5

4-methoxy-benzaldehyde

4-methoxybenzaldehyde O-methyl oxime
70286-37-2, 87861-04-9, 33499-40-0

4-methoxybenzaldehyde O-methyl oxime

Conditions
ConditionsYield
With sodium hydroxide In methanol; water at 0 - 20℃; for 1h;100%
With sodium acetate In ethanol92%
N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

4-methyl-benzoyl chloride
874-60-2

4-methyl-benzoyl chloride

N-methoxy-4-methylbenzamide
25563-06-8

N-methoxy-4-methylbenzamide

Conditions
ConditionsYield
With potassium carbonate In water; ethyl acetate at 0 - 20℃; for 2h; Inert atmosphere;100%
With potassium carbonate In water; ethyl acetate at 0 - 20℃;99%
With potassium carbonate In water; ethyl acetate at 0 - 20℃;93%
N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

4-methoxy-benzoyl chloride
100-07-2

4-methoxy-benzoyl chloride

N-methoxy-4-methoxylbenzamide
24056-08-4

N-methoxy-4-methoxylbenzamide

Conditions
ConditionsYield
With pyridine In dichloromethane at 20℃; for 2h;100%
With sodium carbonate In water; benzene at 20℃; for 18h; Cooling;98%
With potassium carbonate In water; ethyl acetate at 0 - 20℃;98%
N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

benzyl chloroformate
501-53-1

benzyl chloroformate

O-benzyl-N-methoxycarbamate
121989-74-0

O-benzyl-N-methoxycarbamate

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0 - 20℃; for 5h;100%
With sodium carbonate In water; benzene for 5h; Ambient temperature;98%
With sodium carbonate In water; toluene at 20℃; for 5h;54%
N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

2α-azido-5α-cholestan-3-one
35647-02-0

2α-azido-5α-cholestan-3-one

2α-Azido-3-(methoxyimino)cholestane

2α-Azido-3-(methoxyimino)cholestane

Conditions
ConditionsYield
With pyridine at 0℃; for 3.5h;100%
2-(4-methoxyphenyl)-2,3-dihydro-1H-inden-1-one
1086-43-7

2-(4-methoxyphenyl)-2,3-dihydro-1H-inden-1-one

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

2-(4-methoxyphenyl)-1-indanone oxime methyl ether
145962-42-1

2-(4-methoxyphenyl)-1-indanone oxime methyl ether

Conditions
ConditionsYield
With sodium acetate In methanol Ambient temperature;100%
N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

2-(N-allylbenzylamino)-4-oxo-4H-pyrido<1,2-a>pyrimidine 3-carboxaldehyde

2-(N-allylbenzylamino)-4-oxo-4H-pyrido<1,2-a>pyrimidine 3-carboxaldehyde

2-(Allyl-benzyl-amino)-4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carbaldehyde O-methyl-oxime
183968-81-2

2-(Allyl-benzyl-amino)-4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carbaldehyde O-methyl-oxime

Conditions
ConditionsYield
With sodium acetate In methanol for 3h; Ambient temperature;100%
N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

2--4-oxo-4H-pyrido<1,2-a>pyrimidine-3-carbaldehyde

2--4-oxo-4H-pyrido<1,2-a>pyrimidine-3-carbaldehyde

2-[Benzyl-((E)-but-2-enyl)-amino]-4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carbaldehyde O-methyl-oxime

2-[Benzyl-((E)-but-2-enyl)-amino]-4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carbaldehyde O-methyl-oxime

Conditions
ConditionsYield
With sodium acetate In methanol for 3.5h; Ambient temperature;100%
N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

benzaldehyde
100-52-7

benzaldehyde

(E)-benzaldehyde O-methyloxime
10229-53-5

(E)-benzaldehyde O-methyloxime

Conditions
ConditionsYield
With sodium acetate In tetrahydrofuran; water at 20℃; for 4h;100%
With hydrogenchloride In ethanol Heating;71%
With sodium acetate In ethanol; water for 2h; Reflux;68%
platanic acid
6060-06-6

platanic acid

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-9-Hydroxy-1-{1-[(Z)-methoxyimino]-ethyl}-5a,5b,8,8,11a-pentamethyl-icosahydro-cyclopenta[a]chrysene-3a-carboxylic acid

(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-9-Hydroxy-1-{1-[(Z)-methoxyimino]-ethyl}-5a,5b,8,8,11a-pentamethyl-icosahydro-cyclopenta[a]chrysene-3a-carboxylic acid

Conditions
ConditionsYield
With sodium acetate In methanol100%
N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

C17H24O5

C17H24O5

N-methoxy-4-(4-methoxy-3-methyl-phenyl)-butyramide
626239-69-8

N-methoxy-4-(4-methoxy-3-methyl-phenyl)-butyramide

Conditions
ConditionsYield
With triethylamine at 0℃; for 1h;100%
3-(2,4-dimethoxy-phenyl)-2-methyl-propionic acid

3-(2,4-dimethoxy-phenyl)-2-methyl-propionic acid

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

O-methyl (+/-)-3-(2,4-dimethoxyphenyl)-2-methylpropiohydroxamate

O-methyl (+/-)-3-(2,4-dimethoxyphenyl)-2-methylpropiohydroxamate

Conditions
ConditionsYield
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 20℃; for 9h;100%
5-formyl-1-methyl-2-tert-butylindolizine
906361-94-2

5-formyl-1-methyl-2-tert-butylindolizine

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

2-tert-butyl-1-methyl-indolizine-5-carbaldehyde O-methyl-oxime

2-tert-butyl-1-methyl-indolizine-5-carbaldehyde O-methyl-oxime

Conditions
ConditionsYield
With pyridine In ethanol at 20℃; for 5h;100%
N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

indole-2,3-dione
91-56-5

indole-2,3-dione

1H-indole-2,3-dione 3-(O-methyloxime)
107976-78-3

1H-indole-2,3-dione 3-(O-methyloxime)

Conditions
ConditionsYield
With dipotassium hydrogenphosphate In methanol at 20℃; for 2h;100%
With sodium hydrogencarbonate In methanol; water at 50℃; for 8h;92%
With sodium hydrogencarbonate In methanol; water at 20℃; for 1.08333h;80%
methyl 2-[(4-hydroxyphenyl)methyl]-3-oxopentanoate
361576-47-8

methyl 2-[(4-hydroxyphenyl)methyl]-3-oxopentanoate

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

2-(4-hydroxy-benzyl)-3-methoxyimino-pentanoic acid methyl ester
851181-19-6

2-(4-hydroxy-benzyl)-3-methoxyimino-pentanoic acid methyl ester

Conditions
ConditionsYield
With sodium acetate In methanol at 20℃; for 5h;100%
With sodium acetate In methanol90%
N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

4-methoxy-benzaldehyde
123-11-5

4-methoxy-benzaldehyde

4-methoxy-benzaldehyde-(O-methyl-seqtrans-oxime )
70286-37-2

4-methoxy-benzaldehyde-(O-methyl-seqtrans-oxime )

Conditions
ConditionsYield
100%
methyl (E)-3-methoxy-2-trans[2-(3-(2-(1-oxoheptyl-1-yl)cyclopropyl)phenoxymethyl)phenyl]-2-propenoate

methyl (E)-3-methoxy-2-trans[2-(3-(2-(1-oxoheptyl-1-yl)cyclopropyl)phenoxymethyl)phenyl]-2-propenoate

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

methyl 3-methoxy-2-trans-[2-(3-(2-(methoximinohept-1-yl)cyclopropyl)phenoxymethyl)phenyl]-2-propenoate

methyl 3-methoxy-2-trans-[2-(3-(2-(methoximinohept-1-yl)cyclopropyl)phenoxymethyl)phenyl]-2-propenoate

Conditions
ConditionsYield
In methanol at 20℃; for 12h;100%
C19H15N5O
672318-77-3

C19H15N5O

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

C20H18N6O
672319-03-8

C20H18N6O

Conditions
ConditionsYield
With pyridine In tetrahydrofuran; dichloromethane at 25℃; for 72h;100%
2-(2,3,5-trimethylcyclopentadienyl)benzaldehyde

2-(2,3,5-trimethylcyclopentadienyl)benzaldehyde

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

O-methyl-2-(2,3,5-trimethylcyclopentadienyl)benzaldehyde oxime

O-methyl-2-(2,3,5-trimethylcyclopentadienyl)benzaldehyde oxime

Conditions
ConditionsYield
With sodium acetate In tetrahydrofuran; water at 25℃; for 0.5h;100%
(5-fluoro-4-methyl-3-thioxo-3,4-dihydro-2H-benzo[1,4]oxazin-7-yl)-carbamic acid benzyl ester
864074-10-2

(5-fluoro-4-methyl-3-thioxo-3,4-dihydro-2H-benzo[1,4]oxazin-7-yl)-carbamic acid benzyl ester

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

(5-fluoro-3-methoxyimino-4-methyl-3,4-dihydro-2H-benzo[1,4]oxazin-7-yl)-carbamic acid benzyl ester

(5-fluoro-3-methoxyimino-4-methyl-3,4-dihydro-2H-benzo[1,4]oxazin-7-yl)-carbamic acid benzyl ester

Conditions
ConditionsYield
With pyridine at 70℃;100%
4-Trifluoromethylbenzaldehyde
455-19-6

4-Trifluoromethylbenzaldehyde

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

(E)-4-trifluoromethylbenzaldehyde O-methyloxime
1012051-66-9

(E)-4-trifluoromethylbenzaldehyde O-methyloxime

Conditions
ConditionsYield
100%
With sodium acetate In ethanol; water at 70℃; for 2h;
3,4 difluorobenzaldehyde
34036-07-2

3,4 difluorobenzaldehyde

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

3,4-difluorobenzaldehyde O-methyloxime
646051-28-7

3,4-difluorobenzaldehyde O-methyloxime

Conditions
ConditionsYield
100%
N-(3-oxobutyl)phthalimide
3783-77-5

N-(3-oxobutyl)phthalimide

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

N-[3-(N-methoxyimino)butyl]-phthalimide

N-[3-(N-methoxyimino)butyl]-phthalimide

Conditions
ConditionsYield
With sodium hydroxide In methanol100%
3-(3-acetyl-4-chloro-6-fluoro-2-methylbenzofuran-7-yl)-1-methyl-6-trifluoromethyluracil
193676-14-1

3-(3-acetyl-4-chloro-6-fluoro-2-methylbenzofuran-7-yl)-1-methyl-6-trifluoromethyluracil

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

3-[4-chloro-6-fluoro-3-(1-methoxyiminoethyl)-2-methylbenzofuran-7-yl]-1-methyl-6-trifluoromethyluracil

3-[4-chloro-6-fluoro-3-(1-methoxyiminoethyl)-2-methylbenzofuran-7-yl]-1-methyl-6-trifluoromethyluracil

Conditions
ConditionsYield
With potassium acetate In methanol; ethyl acetate100%
C18H20O4
1029697-36-6

C18H20O4

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

C20H26N2O4

C20H26N2O4

Conditions
ConditionsYield
With pyridine; acetic acid at 20 - 40℃; for 2h;100%
1-ethyl-2,3,4,10,10a-pentaaza-cyclopenta[b]fluoren-9-one
941568-39-4

1-ethyl-2,3,4,10,10a-pentaaza-cyclopenta[b]fluoren-9-one

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

1-ethyl-2,3,4,10,10a-pentaaza-cyclopenta[b]fluoren-9-one O-methyl-oxime
1022084-11-2

1-ethyl-2,3,4,10,10a-pentaaza-cyclopenta[b]fluoren-9-one O-methyl-oxime

Conditions
ConditionsYield
With pyridine at 60℃; for 2 - 3h; Molecular sieve;100%
C26H35BrN4O2
1149581-07-6

C26H35BrN4O2

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

4-bromo-2-{2-[4-(diethylamino)phenyl]-2-(methoxyimino)ethyl}-5-[(1R,2R,3R,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-ylamino]pyridazin-3(2H)-one
1149581-81-6

4-bromo-2-{2-[4-(diethylamino)phenyl]-2-(methoxyimino)ethyl}-5-[(1R,2R,3R,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-ylamino]pyridazin-3(2H)-one

Conditions
ConditionsYield
In ethanol at 80℃; for 1h;100%
Stanolone
521-18-6

Stanolone

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

stanolone 3-Z,E-methyloxime

stanolone 3-Z,E-methyloxime

Conditions
ConditionsYield
With triethylamine; sodium hydroxide In tetrahydrofuran; water at 20 - 60℃; for 5h;100%
8-fluoro-2,2-dimethyl-7-(piperidin-1-yl)chroman-4-one
1221444-84-3

8-fluoro-2,2-dimethyl-7-(piperidin-1-yl)chroman-4-one

N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

(E)-8-fluoro-2,2-dimethyl-7-(piperidin-1-yl)chroman-4-one O-methyl oxime
1221444-85-4

(E)-8-fluoro-2,2-dimethyl-7-(piperidin-1-yl)chroman-4-one O-methyl oxime

Conditions
ConditionsYield
With pyridine at 20℃; for 16h;100%
With pyridine at 20℃; for 16h;100%

Methoxyammonium chloride Chemical Properties

Detail of METHYLOXYLAMMONIUM CHLORIDE(593-56-6).
Molecular Structure:

Name:METHYLOXYLAMMONIUM CHLORIDE
CAS Number:593-56-6
Molecular Formula:CH5NO.ClH
Molecular Weight:83.53
EINECS:209-798-7
Density:0.854g/cm3
Melting Point:148-153°
Boiling Point:105-110°
liansport Information:UN 3261
Properties:Prisms.
density:1.1 g/mL at 25°
refractive index:n20/D 1.4021 
Water Solubility:SOLUBLE
Sensitive:Hygroscopic
Merck:14,5989
BRN:3589723
CAS DataBase Reference:593-56-6(CAS DataBase Reference)
EPA Substance Registry System:593-56-6(EPA Substance)
Synonyms of METHYLOXYLAMMONIUM CHLORIDE(593-56-6):O-METHYLHYDROXYAMINE HYDROCHLORIDE;O-METHYLHYDROXYLAMINE HCL;O-METHYLHYDROXYLAMINE HYDROCHLORIDE;O-METHYLHYDROXYLAMMONIUM CHLORIDE;MOX REAGENT;MOX(TM) REAGENT;HYDROXYLAMINE METHYL ETHER HYDROCHLORIDE;MAH
 

Methoxyammonium chloride Uses

METHYLOXYLAMMONIUM CHLORIDE(593-56-6) can be used as methoxy amine, but also used in the production of drugs cefuroxime side chain and other drugs.

Methoxyammonium chloride Toxicity Data With Reference

1.    

oms-bcs 900 mmol/L

    DKBSAS    Doklady Biological Sciences (English Translation). 257 (1981),154.
2.    

msc-ham:lng 2 g/L

    SOGEBZ    Soviet Genetics. Translation of GNKAA5. 11 (1975),475.

Methoxyammonium chloride Consensus Reports

Reported in EPA TSCA Inventory. EPA Genetic Toxicology Program.

Methoxyammonium chloride Safety Profile

Mutation data reported. When heated to decomposition it emits very toxic fumes of HCl, NH3 and NOx. See also AMINES.
Safety Information of METHYLOXYLAMMONIUM CHLORIDE(593-56-6).
Hazard Codes:C,Xi,N
Risk Statements:34-36/37/38-50-43-20/21/22
Safety Statements:3-24-26-36/37/39-45-61-24/25-27
RIDADR:UN 3265 8/PG 2
WGK Germany:3
RTECS:NC3980000
F:3-10
Hazard Note:Corrosive/Hygroscopic
HazardClass:8
PackingGroup:III
 

Methoxyammonium chloride Specification

Stability and Reactivity of METHYLOXYLAMMONIUM CHLORIDE(593-56-6).
Chemical Stability: Hygroscopic: absorbs moisture or water from the air. 
Conditions to Avoid: Incompatible materials, exposure to moist air or water. 
Incompatibilities with Other Materials Exposure to moist air or water, strong bases, acid chlorides, acid anhydrides. 
Hazardous Decomposition Products Hydrogen chloride, nitrogen oxides, carbon monoxide, irritating and toxic fumes and gases, carbon dioxide, nitrogen. 
Hazardous Polymerization Has not been reported. 
First Aid Measures of METHYLOXYLAMMONIUM CHLORIDE(593-56-6).
Eyes: Immediately flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Get medical aid immediately.
Skin: Get medical aid immediately. Immediately flush skin with plenty of water for at least 15 minutes while removing contaminated clothing and shoes. 
Ingestion: Do not induce vomiting. Get medical aid immediately. 
Inhalation: Get medical aid immediately. Remove from exposure and move to fresh air immediately. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. 
Notes to Physician: Treat symptomatically and supportively. 
Handling and Storage of METHYLOXYLAMMONIUM CHLORIDE(593-56-6).
Handling: Do not breathe dust, vapor, mist, or gas. Do not get in eyes, on skin, or on clothing. Do not ingest or inhale. Use only in a chemical fume hood. 
Storage: Store in a cool, dry place. Store in a tightly closed container. Corrosives area. 
 

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