(R)-2-Aminobutanamide hydrochloride

Base Information

• Chemical Name: (R)-2-Aminobutanamide hydrochloride
• CAS No.: 103765-03-3
• Molecular Formula: C4H11ClN2O
• Molecular Weight: 138.60
• Hs Code.: 2924199090
• European Community (EC) Number: 624-494-8
• DSSTox Substance ID: DTXSID70584887
• Mol file: 103765-03-3.mol

Synonyms:103765-03-3;(R)-2-Aminobutanamide hydrochloride;(R)-(-)-2-Aminobutanamide hydrochloride;(R)-2-Aminobutanamide HCl;(2R)-2-Aminobutanamide hydrochloride;(2R)-2-aminobutanamide;hydrochloride;(R)-( C)-2-Aminobutanamide hydrochloride;MFCD09265126;(R)-(-)-2-AMINOBUTANAMIDE HYDROCHLORIDE, 97per cent;L-2-Aminobutanamide hydrochloride;Butanamide, 2-amino-, monohydrochloride, (R)-;(R)-2-Aminobutyramide hydrochloride;Butanamide, 2-amino-, monohydrochloride, (R)- (9CI);AMY725;SCHEMBL2715205;DTXSID70584887;HDBMIDJFXOYCGK-AENDTGMFSA-N;(R)-2-Aminobutanamidehydrochloride;(R)-2-amino-butanamide hydrochloride;2-(R)-amino-butanamide hydrochloride;AKOS016844304;DS-6607;CS-0011806;EN300-225956;F11533;(R)-(-)-2-Aminobutanamide hydrochloride, 96%;(2R)-2-Aminobutanamide--hydrogen chloride (1/1);J-001033

Chemical Property of (R)-2-Aminobutanamide hydrochloride

Chemical Property:

• Vapor Pressure: 0.00424mmHg at 25°C
• Melting Point: 258-262 °C
• Boiling Point: 274.2 °C at 760 mmHg
• Flash Point: 119.6 °C
• PSA: 69.11000
• LogP: 1.41160
• Storage Temp.: Inert atmosphere,Room Temperature
• Solubility.: DMSO (Sparingly), Methanol (Slightly), Water
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 138.0559907
• Heavy Atom Count: 8
• Complexity: 72.1

Purity/Quality:

98%,99%, ^*data from raw suppliers

(R)-2-AminobutyramideHydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC(C(=O)N)N.Cl
• Isomeric SMILES: CC[C@H](C(=O)N)N.Cl
• Uses: (R)-2-Aminobutyramide Hydrochloride is used as a reagent in the synthesis of a new class of 2-[(arylalkyl)amino]alkanamide derivatives which have anticonvulsant activity.