117032-51-6 Usage
Description
6-(N-TRIFLUOROACETYL)AMINOCAPROIC ACID N-SUCCINIMIDYL ESTER is an amino reactive heterobifunctional crosslinking reagent that is a white solid. It is a chemical compound with unique properties that make it useful in various applications across different industries.
Uses
Used in Pharmaceutical Industry:
6-(N-TRIFLUOROACETYL)AMINOCAPROIC ACID N-SUCCINIMIDYL ESTER is used as a crosslinking agent for the development of novel drug delivery systems. Its amino reactive nature allows for the formation of stable covalent bonds with other molecules, enhancing the stability and bioavailability of pharmaceutical compounds.
Used in Biotechnology Industry:
In the biotechnology industry, 6-(N-TRIFLUOROACETYL)AMINOCAPROIC ACID N-SUCCINIMIDYL ESTER is used as a crosslinking agent for the modification of proteins and other biomolecules. Its ability to form covalent bonds with amino groups enables the creation of new bioconjugates with improved properties, such as increased stability, enhanced activity, or altered specificity.
Used in Research and Development:
6-(N-TRIFLUOROACETYL)AMINOCAPROIC ACID N-SUCCINIMIDYL ESTER is used as a research tool for studying protein-protein interactions, enzyme mechanisms, and other biological processes. Its amino reactive nature allows for the specific labeling or modification of proteins, providing valuable insights into their structure, function, and interactions with other molecules.
Used in Diagnostics:
6-(N-TRIFLUOROACETYL)AMINOCAPROIC ACID N-SUCCINIMIDYL ESTER is used in the development of diagnostic assays and tests. Its ability to form stable covalent bonds with amino groups can be exploited to create highly specific and sensitive detection methods for various analytes, including proteins, peptides, and small molecules.
Used in Material Science:
In the field of material science, 6-(N-TRIFLUOROACETYL)AMINOCAPROIC ACID N-SUCCINIMIDYL ESTER is used as a crosslinking agent for the development of novel materials with enhanced properties. Its ability to form covalent bonds with amino groups can be utilized to create materials with improved mechanical strength, thermal stability, or chemical resistance.
Used in Chemical Synthesis:
6-(N-TRIFLUOROACETYL)AMINOCAPROIC ACID N-SUCCINIMIDYL ESTER is used as a synthetic building block in the preparation of various complex organic molecules. Its unique reactivity and functional groups make it a valuable starting material for the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 117032-51-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,0,3 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 117032-51:
(8*1)+(7*1)+(6*7)+(5*0)+(4*3)+(3*2)+(2*5)+(1*1)=86
86 % 10 = 6
So 117032-51-6 is a valid CAS Registry Number.
117032-51-6Relevant articles and documents
Pattern-based recognition of heparin contaminants by an array of self-assembling fluorescent receptors
Jagt, Richard B. C.,Gomez-Biagi, Rodolfo F.,Nitz, Mark
, p. 1995 - 1997 (2009)
(Figure Presented) Tracking down potential killers: Strong host-guest interactions enable the facile combination of polycationic cyclodextrin binding motifs (blue) with fluorescent reporters (orange) tethered to a hydrophobic guest molecule (dark green). An array of supramolecular fluorescent receptors prepared by this modular approach was used for the pattern-based recognition of negatively charged contaminants in the anticoagulant drug heparin.
NOVEL AZO COMPOUND, USE THEREOF AND METHOD FOR PREPARING SAME
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Paragraph 0056; 0068; 0069; 0120; 0121; 0143; 0144, (2015/06/17)
The present invention provides a novel azo compound having a quenching ability for the material that exhibits a luminescent phenomenon at an excited energy level, a quencher comprising the novel azo compound, a use of the quencher and a method for prepari
In situ formation of N-trifluoroacetoxy succinimide (TFA-NHS): One-pot formation of succinimidyl esters, N-trifluoroacetyl amino acid succinimidyl esters, and N-maleoyl amino acid succinimidyl esters
Leonard, Nicholas M.,Brunckova, Jarmila
experimental part, p. 9169 - 9174 (2011/12/16)
A method for the in situ formation of N-trifluoroacetoxy succinimide (TFA-NHS) and its application in the formation of succinimidyl esters is presented. The developed method provides N-trifluoroacetyl and N-maleoyl amino acid succinimidyl esters from a variety of amino acids using a one-pot, high-yielding protocol. Investigations into the formation of an N-maleoyl amino acid succinimidyl ester supported the proposal of a revised reaction mechanism, and contributed to the optimization of the reaction conditions.
