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DL-tert-Leucine

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DL-tert-Leucine Basic information

Product Name:
DL-tert-Leucine
Synonyms:
  • Valine, 3-methyl-
  • DL-Tle-OH
  • tert-DL-LEUCINE extrapure
  • tert-leucine
  • (±)-2-Amino-3,3-dimethylbutyric acid, DL-α-tert-Butylglycine
  • DL-tert-Butylglycine,99%
  • DL-tert-ButylglycineDL-tert-Leucine
  • TERT-BUTYLGLYCINE
CAS:
33105-81-6
MF:
C6H13NO2
MW:
131.17
EINECS:
608-831-6
Product Categories:
  • Leucine [Leu, L]
  • Unusual Amino Acids
  • Peptide
Mol File:
33105-81-6.mol
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DL-tert-Leucine Chemical Properties

Melting point:
>300 °C (lit.)
Boiling point:
242.49°C (rough estimate)
Density 
1.0975 (rough estimate)
refractive index 
1.4240 (estimate)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
H2O: 0.1 g/mL, clear, colorless
pka
2.39±0.12(Predicted)
form 
Solid
color 
White to off-white
Water Solubility 
soluble
BRN 
1721823
InChI
InChI=1S/C6H13NO2/c1-6(2,3)4(7)5(8)9/h4H,7H2,1-3H3,(H,8,9)
InChIKey
NPDBDJFLKKQMCM-UHFFFAOYSA-N
SMILES
C(O)(=O)C(C(C)(C)C)N
CAS DataBase Reference
33105-81-6(CAS DataBase Reference)
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3
HS Code 
29224995

MSDS

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DL-tert-Leucine Usage And Synthesis

Chemical Properties

white powder

Uses

peptide synthesis

Definition

ChEBI: Tert-butylglycine is a glycine derivative that is glycine with a tertiary butyl group at position 2. It has a role as a metabolite.

reaction suitability

reaction type: solution phase peptide synthesis

Synthesis

26782-71-8

33105-81-6

The general procedure for synthesizing DL-tert-leucine from D-tert-leucine is as follows: Example 3A: A 30% ammonium hydroxide solution (50 mL) was added to the autoclave, followed by D-tert-leucine (5 g). The autoclave was sealed and the mixture was heated to 85°C under stirring conditions and maintained at this temperature for 12 hours of reaction. Upon completion of the reaction, the reaction mixture was cooled and the solution was transferred to a rotary evaporator and concentrated under vacuum at 55 °C. The solid residue obtained after concentration was mixed with acetone (20 mL) with stirring, followed by filtration and drying to finally obtain DL-tert-leucine (4.6 g, 92% yield, of which the L-isomer accounted for 42% and the D-isomer for 58%).

References

[1] Patent: US2012/245379, 2012, A1. Location in patent: Page/Page column 3
[2] Patent: EP2502896, 2012, A1. Location in patent: Page/Page column 4-5

DL-tert-Leucine Preparation Products And Raw materials

Preparation Products

DL-tert-LeucineSupplier

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