Ethyl iminioformate chloride

Ethyl iminioformate chloride - Names and Identifiers

Name	ethyl formimidate hydrochloride
Synonyms	ethyl imidoformate ETHYL FORMALIMIDATE HCL Ethyl iminioformate chloride ethyl formimidate hydrochloride ETHYL FORMIMIDATE HYDROCHLORIDE Ethylformalimidatehydrochloride (Ethoxymethane)imine hydrochloride Formimidic acid ethyl·hydrochloride Methanimidic acid ethyl·hydrochloride
CAS	16694-46-5
InChI	InChI=1/C3H7NO/c1-2-5-3-4/h3-4H,2H2,1H3/b4-3+

Ethyl iminioformate chloride - Physico-chemical Properties

Molecular Formula	C3H8ClNO
Molar Mass	109.55
Density	0.78512 g/cm3(Temp: 25 °C)
Melting Point	75°C (dec.)(lit.)
Boling Point	31.7°C at 760 mmHg
Vapor Presure	597mmHg at 25°C
Storage Condition	2-8°C
Refractive Index	1.388

Ethyl iminioformate chloride - Risk and Safety

Hazard Symbols	Xi - Irritant
Risk Codes	36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description	S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S37/39 - Wear suitable gloves and eye/face protection
WGK Germany	3

Ethyl iminioformate chloride - Introduction

ethyl formimidate hydrochloride, chemical formula C4H11N2O · HCl, is an organic compound. The following is a description of the properties, uses, preparation and safety information of the compound:

Nature:
-Appearance: ethyl formimidate hydrochloride is usually a colorless or light yellow liquid.
-Solubility: It has high solubility in water and can be dissolved in many organic solvents.
-Stability: The compound is usually stable, but care should be taken to avoid contact with strong oxidants or strong acids.

Use:
-medical use: ethyl formimidate hydrochloride is often used as an intermediate or catalyst for the synthesis of drugs, especially in the preparation of amino acids and polypeptide compounds.

Method:
The preparation of ethyl formimidate hydrochloride can be completed through a series of reaction steps. A common method is:
1. The reaction of methyl mercaptan and carbon monoxide to generate formyl mercaptan.
2. Reaction of formyl mercaptan with methylamine acetate to give methylimine ethyl ester.
3. React methylimine ethyl ester with hydrochloric acid to generate ethyl formimidate hydrochloride.

Safety Information:
- ethyl formimidate hydrochloride is generally considered harmful. Appropriate protective equipment such as gloves, glasses and laboratory coats should be worn during operation.
-Avoid inhaling the vapors of the compound to prevent possible respiratory irritation.
-When handling the compound, follow Good Laboratory Practices and ensure that the work area is well ventilated.
-During handling and storage, avoid contact with strong oxidants or strong acids to avoid possible reactions and dangers.

Last Update：2024-04-09 02:00:42