DL-tert-Leucine
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
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)
Safety Information
- Safety Statements
- 22-24/25
- WGK Germany
- 3
- HS Code
- 29224995
MSDS
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
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
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DL-tert-Leucine(33105-81-6)Related Product Information
- 6-Aminocaproic acid
- N-CARBOBENZOXY-DL-LEUCINE
- Methyl 4-tert-butylbenzoate
- Diethylstilbestrol
- tert-Butanol
- Glycine
- tert-Butyl methyl ether
- L-Leucine
- 4-tert-Butylcatechol
- ALTRENOGEST
- L-tert-Leucine
- tert-Butyl hydroperoxide
- tert-Butylbenzene
- tert-Butyldimethylsilyl chloride
- 2-tert-Butylphenol
- D-tert-Butylglycine
- Tris(hydroxymethyl)aminomethane
- DL-Leucine