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N-(tert-Butoxycarbonyl)glycylglycine

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Products Intro: Product Name:N-(tert-Butoxycarbonyl)glycylglycine
CAS:31972-52-8
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CAS:31972-52-8
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CAS:31972-52-8
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Products Intro: Product Name:Boc-Gly-Gly-OH
CAS:31972-52-8
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Products Intro: Product Name:Boc-Gly.Gly
CAS:31972-52-8
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N-(tert-Butoxycarbonyl)glycylglycine manufacturers

  • BOC-Gly-Gly
  • BOC-Gly-Gly pictures
  • $0.00/ kg
  • 2025-09-15
  • CAS:31972-52-8
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 1T+
  • Boc-Gly-Gly
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  • $0.00 / 100g
  • 2025-06-07
  • CAS:31972-52-8
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  • Purity: >95.00%
  • Supply Ability: 100g
N-(tert-Butoxycarbonyl)glycylglycine Basic information
Product Name:N-(tert-Butoxycarbonyl)glycylglycine
Synonyms:BOC-L-GLYCYL GLYCINE;BOC-GLY-GLY-OH;(2-TERT-BUTOXYCARBONYLAMINO-ACETYLAMINO)-ACETIC ACID;N-(2-N-BOC-AMINO-ACETYL)-GLYCINE;BOC-GLYCYLGLYCINE;2-(2-(tert-butoxycarbonylamino)acetamido)acetic acid;N-(tert-Butoxycarbonyl)glycylglycine;Boc-Glycine-Glycine
CAS:31972-52-8
MF:C9H16N2O5
MW:232.23
EINECS:1533716-785-6
Product Categories:amino acid
Mol File:31972-52-8.mol
N-(tert-Butoxycarbonyl)glycylglycine Structure
N-(tert-Butoxycarbonyl)glycylglycine Chemical Properties
Melting point 132 °C
Boiling point 488.1±30.0 °C(Predicted)
density 1.222±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Store in freezer, under -20°C
solubility soluble in Methanol
form Powder
pka3.41±0.10(Predicted)
color White
CAS DataBase Reference31972-52-8(CAS DataBase Reference)
Safety Information
Risk Statements 43
Safety Statements 24/25-36/37
HS Code 2922.19.9690
HazardClass IRRITANT
MSDS Information
N-(tert-Butoxycarbonyl)glycylglycine Usage And Synthesis
Chemical PropertiesWhite powder
UsesBoc-Gly-Gly-OH is a Glycine.html" class="link-product" target="_blank">Glycine (HY-Y0966) derivative[1].
Synthesis
Glycylglycine

556-50-3

Di-tert-butyl dicarbonate

24424-99-5

N-(tert-Butoxycarbonyl)glycylglycine

31972-52-8

GENERAL METHODS: Amino acids or peptides (1 mmol) were added dropwise to a solution of ethanol (1 mL) containing guanidine hydrochloride (15 mmol) and di-tert-butyl dicarbonate (2.5-3 mmol) under stirring conditions, and the temperature of the reaction was maintained at 35-40°C. The reaction mixture was stirred continuously until a clarified solution was formed. Subsequently, the ethanol was removed by evaporation under reduced pressure. The residue was washed sequentially with distilled water (2 mL) and hexane or petroleum ether (2 mL) to obtain high purity N-Boc amino acids or N-Boc peptides. If further improvement of product purity is required, the crude product can be purified by recrystallization.

References[1] Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144. DOI:10.1080/10408398.2012.708368
N-(tert-Butoxycarbonyl)glycylglycine Preparation Products And Raw materials
Raw materialsGlycylglycine-->Di-tert-butyl dicarbonate-->Guanidine hydrochloride-->Ethanol
Tag:N-(tert-Butoxycarbonyl)glycylglycine(31972-52-8) Related Product Information
Ethyl 2-(Chlorosulfonyl)acetate L-Alanyl-L-Glutamine EC 2.3.2.2 Glycylglycine BOC-Glycine N-Carbobenzyloxyglycine tert-Butanol Glycine 4-Hydroxy-D-(-)-2-phenylglycine Phenylacetic acid Acetic anhydride BOC-VAL-GLY-OH BOC-GLY-PRO-OH BOC-LEU-PRO-OH BOC-ALA-ALA-OH BOC-GLN-PRO-OH BOC-ILE-GLY-OH BOC-PHE-PRO-OH

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