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L-tert-Leucine

L-tert-Leucine Structure
CAS No.
20859-02-3
Chemical Name:
L-tert-Leucine
Synonyms
LEUCINE;LEU;H-LEU-OH;Tle;L-tertiary leucine;H-L-LEU-OH;L-Tle-OH;L-tert-Leu-OH;L-A-AMINOISOCAPROIC ACID;(S)-2-Amino-3,3-dimethylbutanoicacid
CBNumber:
CB9853319
Molecular Formula:
C6H13NO2
Molecular Weight:
131.17
MOL File:
20859-02-3.mol
MSDS File:
SDS
Modify Date:
2024/8/21 22:41:43

L-tert-Leucine Properties

Melting point ≥300 °C (lit.)
alpha 6.3 º (c=4, 6 N HCl 200 ºC)
Boiling point 217.7±23.0 °C(Predicted)
Density 1.1720 (estimate)
refractive index -9 ° (C=3, H2O)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility 1 M HCl: 50 mg/mL
form powder
pka 2.39±0.12(Predicted)
color White to almost white
optical activity [α]20/D 9.5°, c = 3 in H2O
Water Solubility 125.5 g/L (20 ºC)
BRN 1721824
InChIKey NPDBDJFLKKQMCM-SCSAIBSYSA-N
CAS DataBase Reference 20859-02-3(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362
Hazard Codes  Xi
Safety Statements  22-24/25
WGK Germany  3
RTECS  OH2850000
Hazard Note  Irritant
HS Code  29224999
NFPA 704
1
0 0

L-tert-Leucine price More Price(5)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 269107 L-tert-Leucine 99% 20859-02-3 5G ₹8172.88 2022-06-14 Buy
Sigma-Aldrich(India) 269107 L-tert-Leucine 99% 20859-02-3 25G ₹27755.3 2022-06-14 Buy
TCI Chemicals (India) L0147 L-tert-Leucine 20859-02-3 1G ₹2500 2022-05-26 Buy
TCI Chemicals (India) L0147 L-tert-Leucine 20859-02-3 5G ₹6500 2022-05-26 Buy
TCI Chemicals (India) L0147 L-tert-Leucine 20859-02-3 25G ₹20700 2022-05-26 Buy
Product number Packaging Price Buy
269107 5G ₹8172.88 Buy
269107 25G ₹27755.3 Buy
L0147 1G ₹2500 Buy
L0147 5G ₹6500 Buy
L0147 25G ₹20700 Buy

L-tert-Leucine Chemical Properties,Uses,Production

Chemical Properties

White to almost white powder

Uses

L-tert-Leucine is an essential amino acid and makes up one third of our muscle protein. It can be used as a food additive. It is used in the formation of sterols. It is used in the production of cobalt oxazoline palladacycles complex, which acts as a catalyst in the rearrangement of prochiral N-aryl trifluoroacetimidates to allylic amides yielded in significantly higher enantioselectivities with the (S)-(pR)-diasteroisomer.

Production Methods

The synthesis method of L-tert-Leucine (L-Tle) includes chemical and biological methods. Compared with traditional chemical synthesis, the enzymatic reduction of chiral keto acid to synthesize the corresponding unnatural amino acid has the advantages of high optical purity, mild reaction conditions, high conversion rate, and environmental friendliness. Currently, enzymatic methods have gradually replaced chemical methods. Some previous research on preparing L-tert-leucine using hydrolase, acyltransferase, and amino acid dehydrogenase has been reported. Among them, the preparation of L-tert-leucine using NADH-dependent L-leucine dehydrogenase (LeuDH, EC 1.4.1.9) has exhibited the most industrial potential. In the presence of NADH and free ammonium, LeuDH can catalyze trimethylpyruvate (TMP) to L-tert-leucine[1-3].

Synthesis Reference(s)

Organic Syntheses, Coll. Vol. 3, p. 523, 1955
Tetrahedron Letters, 19, p. 4625, 1978 DOI: 10.1016/S0040-4039(01)85688-4

General Description

L-tert-Leucine (L-Tle) is an essential non-natural amino acid often used as a template to induce asymmetric synthesis, and the product has high stereoselectivity. It is a non-polar amino acid, and its tert-butyl group has significant hydrophobicity and steric hindrance, which can control molecular conformation in a chemical reaction and form a chiral compound. Hence, L-tert-leucine is commonly used as an inducer or a template in asymmetric synthesis. As a vital chiral intermediate, L-tert-leucine is widely used to synthesise anti-cancer, anti-viral, and biological inhibitors. In addition, L-tert-leucine is an essential additive in the food and cosmetic industry[1].

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(S)-(+)-LEUCINE RARECHEM AB PP 3754 L-A-AMINO-G-METHYL VALERIC ACID L-A-AMINOISOCAPROIC ACID L-2-AMINO-4-METHYLVALERIC ACID LEUCINE, L- LEU LEUCINE FEMA 3297 H-L-LEU-OH H-LEU-OH L-α-tert-Butylglycine L-TERT-LEUCINE, 99% (99% EE/GLC) L-2-(T-BUTYL)GLYCINE (2S)-2-Amino-3,3-dimethylbutanoicacid l-2-tert-butylglycine LEUCINE, L-(P) α-aminoisocaproic acid L-tert-Leucine 99% L-tert-Leucine, 95+% L-α-tert-Butyl-Gly-OH L-tert-Leu-OH L-Tle-OH L-α-tert-Butyl-Gly-OH≥ 99% (Titration) L-tert-Leucine,99%e.e. Tle 3-Methyl-L-valine 97% L-2-Amino-3,3-dimethylbutanoic acid CAS -tert-L T-LEUCINE, T-BUTYLGLYCINE (S)-2-Amino-3,3-dimethylbutanoicacid L-2-Amino-3,3-dimethylbutanoic acid L-tert-Leucine t-Leucine, t-Butylglycine, (S)-2-Amino-3,3-dimethyl-butyric acid (S)-2-Amino-3,3-dimethylbutyric acid L-α-tert-Butylglycine L-tert-Leucine, 99+% L-tert-B-leucine, 99% (-)-L-Pseudoleucine L-Pseudoleucine (2S)-2-AMino-3,3-diMethylbutanoic acid/l-t-leucine by express 2-L-aMino-3,3-diMethylbutyric acid L-(+)-TERT-LEUCINE FOR SYNTHESIS L-tert-Leucine 3 L-tertiary leucine L-tert-Leucine, (2S)-2-Amino-3,3-dimethylbutanoic acid L-tert-Leucine> L-tert-Leucine USP/EP/BP L-α-tert-Butyl-Gly-OH NSC203785 Enzymatic Hydrolysis Amino Acid Powder 80% (OMRI Listed ) L-tert-Leucine,97% L-tert-Butyl-Glycine 20859-02-3 RCHNH2COOH CH33CCHNH2CO2H CH32CHCH2CHNH2COOH H2NCHRCOOH AMINE