Name | Ethoxyamine hydrochloride |
Synonyms | EHH 2-ETHYLHYDROXYAMINEHCL ETHOXYAMINE HYDROCHLORIDE Ethoxyamine hydrochloride ethoxylamine hydrochloride O-ETHYLHYDROXYLAMMONIUM CHLORIDE o-ethyl-hydroxylaminhydrochloride Ethylhydroxylammoniumhydrochloride O-ETHYLHYDROXYLAMINE HYDROCHLORIDE O-Ethylhydroxylamine hydrochloride |
CAS | 3332-29-4 |
EINECS | 222-060-9 |
InChI | InChI=1/C2H7NO.ClH/c1-2-4-3;/h2-3H2,1H3;1H |
InChIKey | NUXCOKIYARRTDC-UHFFFAOYSA-N |
Molecular Formula | C2H8ClNO |
Molar Mass | 97.54 |
Melting Point | 130-133°C(lit.) |
Boling Point | 75.8°C at 760 mmHg |
Flash Point | 5.9°C |
Water Solubility | Soluble in water |
Vapor Presure | 104mmHg at 25°C |
Appearance | Powder, Crystals or Flakes |
Color | Dark gray |
BRN | 3606639 |
PH | pH(50g/l, 25℃) : 2.3~2.7 |
Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
Sensitive | Easily absorbing moisture |
MDL | MFCD00799598 |
Physical and Chemical Properties | Appearance: white or yellowish crystals
Melting Point: 130.0-133.0 ° C moisture: ≤ 0.5% purity G C :≥ 99.0% solubility: soluble in water, soluble in ethanol |
Use | It is an important pesticide raw material for the production of herbicides such as benzene ketone, benzene ketone, and |
Hazard Symbols | Xi - Irritant |
Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. R34 - Causes burns R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. |
UN IDs | 3261 |
WGK Germany | 3 |
FLUKA BRAND F CODES | 3-10 |
HS Code | 29280000 |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
Uses | Ethoxyamine hydrochloride is an intermediate of the herbicides rare pyridine, thiacidone and trimoloxone. It is an intermediate for the production of the pesticide alkynidine It is used to produce herbicides such as phenoxone, alkenone, and dilute oxadir. It is an important pesticide raw material |
Production method | The preparation method is to react ethyl acetate and hydroxylamine sulfate in the presence of alkali, and the resulting reactant is ethylated with ethyl sulfate, and then Reacts in hydrochloric acid to obtain the product. If the product reacts with a base, ethoxyamine is obtained. |