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N-6-Trifluoroacetyl-L-lysine

CAS No.
10009-20-8
Chemical Name:
N-6-Trifluoroacetyl-L-lysine
Synonyms
H-LYS(TFA)-OH;N6-(2,2,2-Trifluoroacetyl)-L-lysine;Ε-TFA-LYSINE;LYR(TFA)-TYR;LYS(TFA)-TYR;L-Lys(Tfa)-OH;LYSINE(TFA)-OH;H-LYS(CF3CO)-OH;EPSILON-TFA-LYSINE;n(epsilon)-trifluoro
CBNumber:
CB4249490
Molecular Formula:
C8H13F3N2O3
Molecular Weight:
242.2
MDL Number:
MFCD00037223
MOL File:
10009-20-8.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 02:02:48
Product description Number Pack Size Price
Nε-Trifluoroacetyl-L-lysine ≥96.0% (TLC) 53604 5G $77.8
Nε-Trifluoroacetyl-L-lysine ≥96.0% (TLC) 53604 25g $229
Nε-Trifluoroacetyl-L-lysine >98.0%(T) T2815 5g $19
Nε-Trifluoroacetyl-L-lysine >98.0%(T) T2815 25g $51
Ne-Trifluoroacetyl-L-lysine Asreported 285625 10g $333
More product size

N-6-Trifluoroacetyl-L-lysine Properties

Melting point 258
Boiling point 382.5±42.0 °C(Predicted)
Density 1.4
storage temp. Keep in dark place,Sealed in dry,2-8°C
solubility 2 M HCl: 10 mg/mL, clear, colorless
pka 2.51±0.24(Predicted)
form Solid
color Off-White
BRN 2122429
Major Application peptide synthesis
InChI InChI=1S/C8H13F3N2O3/c9-8(10,11)7(16)13-4-2-1-3-5(12)6(14)15/h5H,1-4,12H2,(H,13,16)(H,14,15)/t5-/m0/s1
InChIKey PZZHRSVBHRVIMI-YFKPBYRVSA-N
SMILES C(O)(=O)[C@H](CCCCNC(C(F)(F)F)=O)N
UNSPSC Code 12352209
NACRES NA.26

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
PPE Eyeshields, Gloves, type N95 (US)
Safety Statements  22-24/25
WGK Germany  1
10
HS Code  29241990
Storage Class 11 - Combustible Solids
REACH Registrations Active

N-6-Trifluoroacetyl-L-lysine price More Price(88)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 53604 Nε-Trifluoroacetyl-L-lysine ≥96.0% (TLC) 10009-20-8 5G $77.8 2025-07-31 Buy
Sigma-Aldrich 53604 Nε-Trifluoroacetyl-L-lysine ≥96.0% (TLC) 10009-20-8 25g $229 2023-06-20 Buy
TCI Chemical T2815 Nε-Trifluoroacetyl-L-lysine >98.0%(T) 10009-20-8 5g $19 2026-04-30 Buy
TCI Chemical T2815 Nε-Trifluoroacetyl-L-lysine >98.0%(T) 10009-20-8 25g $51 2026-04-30 Buy
Usbiological 285625 Ne-Trifluoroacetyl-L-lysine Asreported 10009-20-8 10g $333 2026-06-03 Buy
Product number Packaging Price Buy
53604 5G $77.8 Buy
53604 25g $229 Buy
T2815 5g $19 Buy
T2815 25g $51 Buy
285625 10g $333 Buy

N-6-Trifluoroacetyl-L-lysine Chemical Properties,Uses,Production

Chemical Properties

Off-White Solid

Uses

A cysteine conjugate metabolite adduct formation with specific mitochondrial proteins using antibodies raised against halothane metabolite adducts.

Definition

ChEBI: An N6-acyl-L-lysine where the N6-acyl group is trifluoroacetyl.

Biological Activity

Nε-Trifluoroacetyl-L-lysine is an inhibitor of L-lysine cyclodeaminase.', 'Nε-Trifluoroacetyl-L-lysine may be used to create synthetic organic polypeptides useful for nonaqueous capillary electrophoresis (NACE).

Synthesis

Ethyl trifluoroacetate

383-63-1

L-Lysine hydrochloride

657-27-2

N-6-Trifluoroacetyl-L-lysine

10009-20-8

1. Sodium ethanolate solution was prepared by dissolving sodium metal (4.6 g, 0.2 mol) in 200 mL of anhydrous ethanol. 2. L-lysine hydrochloride (18.25 g, 0.1 mol) was slowly added to the above solution under stirring conditions. 3. The reaction mixture was stirred continuously for 1 hour, followed by filtration to remove the insoluble precipitate. 4. The filtrate was cooled in an ice bath and ethyl trifluoroacetate (21.3 g, 0.15 mol) was added slowly and dropwise with vigorous stirring. 5. The reaction mixture was gradually warmed to room temperature and stirring was continued for 2 hours. 6. Acetic acid (6 g, 0.1 mol) was added to neutralize the reaction system and the resulting precipitate was subsequently collected by filtration. 7. The precipitate was washed sequentially with ethanol and acetone and dried to give the target product trifluoroacetyl lysine. 8. Yield: 15 g (62% yield). 9. MALDI-TOF mass spectrometry (positive ion mode): m/z 242.455 ([M+H]+, relative abundance 67%).

References

[1] Russian Journal of Organic Chemistry, 2007, vol. 43, # 10, p. 1427 - 1431
[2] Patent: WO2009/114809, 2009, A1. Location in patent: Page/Page column 7
[3] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 1, p. 255 - 258

N-6-Trifluoroacetyl-L-lysine Preparation Products And Raw materials

Global( 426)Suppliers
Supplier Tel Email Country ProdList Advantage
airuikechemical co., ltd.
+86-18353166132 sales02@airuikechemical.com China 983 58
Capot Chemical Co.,Ltd.
+86-(0)57185586718 +86-13336195806 sales@capot.com China 29640 60
Shanghai Daken Advanced Materials Co.,Ltd
+86-2158073036 info@dakenam.com China 14014 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21586 55
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 33024 60
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29812 58
Jinan Finer Chemical Co., Ltd
+86-531-88989536 +86-15508631887 sales@finerchem.com China 2950 58
Shandong chuangyingchemical Co., Ltd.
18853181302 sale@chuangyingchem.com CHINA 5906 58
BOC Sciences
+1-631-485-4226 inquiry@bocsci.com United States 19936 58
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63687 58

View Lastest Price from N-6-Trifluoroacetyl-L-lysine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
H-Lys(Tfa)-OH pictures 2026-05-11 H-Lys(Tfa)-OH
10009-20-8
$29.00 99.35% 10g TargetMol Chemicals Inc.
H-Lys(Tfa)-OH pictures 2026-05-11 H-Lys(Tfa)-OH
10009-20-8
$29.00 99.35% 10g TargetMol Chemicals Inc.
N-6-Trifluoroacetyl-L-lysine pictures 2025-04-04 N-6-Trifluoroacetyl-L-lysine
10009-20-8
1KG 98% 1Ton Henan Aochuang Chemical Co.,Ltd.

N-6-Trifluoroacetyl-L-lysine Spectrum

H-LYS(CF3CO)-OH EPSILON-TFA-LYSINE LYSINE(TFA)-OH N-EPSILON-TRIFLUOROACETYL-L-LYSINE N6-TRIFLUOROACETYL-L-LYSINE N6-Trrifluoroacetyl-L-lysine(for Lisinopril) N6-Trifluoroacetyl-L-lysine 98% INTERMEDIATE OF QUINAPRIL/N6-TRIFLUOROACETYL-L-LYSINE N-6-TRIFLUORO ACETYL-L-LYSINE ( LISINOPRIL INTERMEDIATE ) N6-Trifluoroacetyl-L-lysine98% N(6)-Trifluoracetyl-L-Lysin Ε-TFA-LYSINE N-ε-Trifluoroacetyl-L-lysine N1-Trifluoroacetyl-L-Lysine N6-Trifluoroaccety-L-lysine N6-Trifluoroacetyl-L-lysine (for lisinopril) (2S)-2-amino-6-(2,2,2-trifluoroacetamido)hexanoic acid (2S)-2-amino-6-(trifluoroacetamido)hexanoic acid (S)-2-aMino-6-(2,2,2-trifluoroacetaMido)hexanoic acid n(epsilon)-trifluoro N-E-TRIFLUOROACETYL-L-LYSINE Trifluoroacetyllysine LYR(TFA)-TYR N6-Tryfluoro Acetyl-L-Lysine Nε-Trifluoroacetyl-L-lysine (S)-2-AMino-6-(2,2,2-trifluoro-acetylaMino)-hexanoic acid LYS(TFA)-TYR L-Lys(Tfa)-OH Nε-Trifluoroacetyl-L-lysine≥ 99% (Assay) ε-TFA-lysine H-Lys(Tfa)-OH Lys(tfa)-OH / K(Tfa) L-Lysine, N6-(2,2,2-trifluoroacetyl)- N-6-Trifluoroacetyl-L-lysine USP/EP/BP N-6-Trifluoroacetyl-L-Lysine extrapure, 98% Nε-Trifluoroacetyl Lysine Nε-Trifluoroacetyl-L-lysine (S)-2-Amino-6-(2,2,2-trifluoro-acetcarboxcarboxcarboxamido)-hexanoic acid H-LYS(TFA)-OH N6-(2,2,2-Trifluoroacetyl)-L-lysine 10009-20-8 10009-60-8 C8H13F3N2O3 C8H13N2O3F3 Specialty Synthesis Lysine Peptide Synthesis Amino Acid Derivatives Amino Acids & Derivatives, Metabolites & Impurities Amino Acids & Derivatives Metabolites & Impurities amino acid API intermediates Chemical intermediate for LISINOPRIL 10009-20-8