Ethanimidamide, hydrochloride (1:1)
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Ethanimidamide, hydrochloride (1:1)
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CAS No:
124-42-5
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Formula:
C2H6N2.ClH
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Chemical Name:
Ethanimidamide, hydrochloride (1:1)
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Synonyms:
Ethanimidamide,hydrochloride (1:1);Acetamidine,monohydrochloride;Ethanimidamide,monohydrochloride;Acetamidine,hydrochloride;Acediamine hydrochloride;α-Amino-α-iminoethane hydrochloride;Ethanamidine hydrochloride;SN 4455;Acetamidinium chloride;Acetimidinium chloride;Ethanimidamide,hydrochloride;Methylamidine hydrochloride;Acetamidine hydrochloride;Acetimidamide hydrochloride;51991-59-4;68473-12-1;143504-21-6
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CAS No:
Ethanimidamide, hydrochloride (1:1) Basic Attributes
94.54
94.029778
3591762
204-700-9
M2026K4JCF
7595
DTXSID2059564
29252000
Characteristics
49.9
1.54430
White to cream Crystalline Powder, Crystals and/or Chunks
1.0596 (rough estimate)
177.5 °C
129.78°C (rough estimate)
26.1ºC
1.5500 (estimate)
1 g/mL
Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.
176mmHg at 25°C
Safety Information
NONH for all modes of transport
3
36/37/38-36/38
26-37/39
Xi
Stable at room temperature in closed containers under normal storage and handling conditions.
P261-P305 + P351 + P338
H315-H319-H335
|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 49 companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Ethanimidamide, hydrochloride (1:1) Use and Manufacturing
It is obtained by addition and ammoniation of acetonitrile, hydrochloric acid and methanol. Make methanol circulate in the turbulent ball tower, the pressure is less than 26.6kPa, and pass dry hydrogen chloride under cooling to make a 45% hydrogen chloride methanol solution. Then put it into the reaction tank, stir and cool to 10-5°C, add acetonitrile dropwise, and keep it at 15-20°C for 6h to obtain iminomethyl ethyl ether hydrochloride. Put it into the pre-prepared 13% ammonia methanol solution, ammolyze it at 0-40℃, keep the pH value 7-8, stir for 2-3h, cool to below 30℃, centrifuge and filter out ammonium chloride. The filtrate recovers methanol, cools and filters to obtain a finished product. Weight feeding ratio: acetonitrile: hydrogen chloride methanol solution (45%): ammonia: methanol=1:3:1.05:4.3. The yield is 82%-85%.
Used in the synthesis of imidazoles, pyrimidines, triazines antibiotics, but also in the synthesis of vitamin B1
Ethanimidamide, hydrochloride (1:1): ACTIVE
Computed Properties
Molecular Weight:94.54
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:1
Exact Mass:94.0297759
Monoisotopic Mass:94.0297759
Topological Polar Surface Area:49.9
Heavy Atom Count:5
Complexity:31
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
Drug Function and Efficacy
Promote gastrointestinal motility, increase gastrointestinal electrical amplitude, etc.
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Ethanimidamide, hydrochloride (1:1)
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