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Glycine tert-butyl ester hydrochloride, 99%, Thermo Scientific Chemicals
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Catalog number L17116.06
also known as L17116-06
Price (USD)/ Each
153.65
Online exclusive
171.00 Save 17.35 (10%)
-
Quantity:
5 g
Price (USD)/ Each
153.65
Online exclusive
171.00 Save 17.35 (10%)
Glycine tert-butyl ester hydrochloride, 99%, Thermo Scientific Chemicals
Catalog numberL17116.06
Price (USD)/ Each
153.65
Online exclusive
171.00 Save 17.35 (10%)
-
Chemical Identifiers
CAS27532-96-3
IUPAC Name2-(tert-butoxy)-2-oxoethan-1-aminium
Molecular FormulaC6H14NO2
InChI KeySJMDMGHPMLKLHQ-UHFFFAOYSA-O
SMILESCC(C)(C)OC(=O)C[NH3+]
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Specifications
Specification Sheet
Specification SheetAssay (Freebase GC)≥96.0%
Appearance (Color)White to pale cream
Assay (Titration ex Chloride)≥96.0 to ≤104.0%
FormCrystals or powder or crystalline powder or lumps
Identification (FTIR)Conforms
Glycine t-butyl ester hydrochloride is a substituted Glycine used as parakeratosis inhibitor.
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 t-butyl ester hydrochloride is a substituted Glycine used as parakeratosis inhibitor.
Solubility
Soluble in methanol and water
Notes
Keep container tightly closed. Store away from oxidizing agents.
Glycine t-butyl ester hydrochloride is a substituted Glycine used as parakeratosis inhibitor.
Solubility
Soluble in methanol and water
Notes
Keep container tightly closed. Store away from oxidizing agents.
RUO – Research Use Only
General References:
- H. R. Allcock.; T. J. Fuller.; D. P. Mack.; K. Matsumura.; Karen M. Smeltz. Synthesis of Poly[(amino acid alkyl ester)phosphazenes]. Macromolecules. 1977, 10 (4), 824-830.
- Hiroyuki Ishiwata.; Hiroki Sone.; Hideo Kigoshi.; Kiyoyuki Yamada. Total Synthesis of Doliculide, a Potent Cytotoxic Cyclodepsipeptide from the Japanese Sea Hare Dolabella auricularia. J. Org. Chem. 1994, 59 (17), 4712-4713.