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Glycine methyl ester hydrochloride, 99%, Thermo Scientific Chemicals
化学物質識別子
CAS5680-79-5
IUPAC Namehydrogen methyl 2-aminoacetate chloride
Molecular FormulaC3H8ClNO2
InChI KeyCOQRGFWWJBEXRC-UHFFFAOYSA-N
SMILES[H+].[Cl-].COC(=O)CN
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仕様
スペックシート
スペックシートAppearance (Color)White
FormCrystals or powder or crystalline powder or fused/lumpy solid
Assay (Titration ex Chloride)≥98.5 to ≤101.5%
Identification (FTIR)Conforms
Glycine methyl ester hydrochloride a non-essential amino acid used for human development.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Glycine methyl ester hydrochloride a non-essential amino acid used for human development.
Solubility
Soluble in water (2% w/v) and methanol (50 mg/ml).
Notes
Hygroscopic. Store in cool, dry place in tightly closed containers. Store away from oxidizing agent and water/moisture.
Glycine methyl ester hydrochloride a non-essential amino acid used for human development.
Solubility
Soluble in water (2% w/v) and methanol (50 mg/ml).
Notes
Hygroscopic. Store in cool, dry place in tightly closed containers. Store away from oxidizing agent and water/moisture.
RUO – Research Use Only
General References:
- Reuben G. Jones. Studies on imidazoles. II. The Synthesis of 5-imidazolecarboxylates from glycine and substituted glycine esters. J. Am. Chem. Soc. 1949, 71 (2), 644-647.
- Kim L. Dueholm, Michael Egholm; Ole Buchardta. An Efficient Synthesis Of Boc-Aminoacetaldehyde And Its Application To The Synthesis Of N-(2-Boc-Aminoethyl)Glycine Esters. J. Am. Chem. Soc. 1993, 25 (4), 457-461.