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15579-00-7

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15579-00-7 Usage

Description

3-[(2-AMINOETHYL)DITHIO]PROPIONIC ACID, also known as Aminoethyl-SS-propionic acid, is a cleavable compound that features a terminal amine and carboxylic acid group. It is characterized by its disulfide bonds, which can be cleaved using Dithiothreitol (DTT) reagent. 3-[(2-AMINOETHYL)DITHIO]PROPIONIC ACID is a white solid and is known for its ability to react with various chemical groups, making it a versatile molecule in the field of biochemistry.

Uses

Used in Biochemistry and Molecular Biology:
3-[(2-AMINOETHYL)DITHIO]PROPIONIC ACID is used as a reversible immobilization or crosslinking reagent for various applications in biochemistry and molecular biology. The terminal amine can react with carboxylic acid, activated NHS esters, and other carbonyl compounds, while the terminal carboxylic acid can form a stable amide bond with primary amines in the presence of activators such as EDC and HATU. This reagent is particularly useful for the study of protein-protein interactions, enzyme immobilization, and the development of biosensors.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-[(2-AMINOETHYL)DITHIO]PROPIONIC ACID is used as a key component in the development of drug delivery systems. Its ability to form stable amide bonds and react with various chemical groups makes it an ideal candidate for the design of targeted drug delivery systems, which can improve the efficacy and bioavailability of therapeutic agents.
Used in Materials Science:
3-[(2-AMINOETHYL)DITHIO]PROPIONIC ACID is also utilized in materials science for the development of novel biocompatible materials. Its chemical properties allow for the creation of materials with specific interactions and functionalities, which can be applied in areas such as tissue engineering, biosensors, and drug delivery devices.

Check Digit Verification of cas no

The CAS Registry Mumber 15579-00-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,7 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15579-00:
(7*1)+(6*5)+(5*5)+(4*7)+(3*9)+(2*0)+(1*0)=117
117 % 10 = 7
So 15579-00-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H11NO2S2/c6-2-4-10-9-3-1-5(7)8/h1-4,6H2,(H,7,8)

15579-00-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-aminoethyldisulfanyl)propanoic acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15579-00-7 SDS

15579-00-7Relevant articles and documents

DOLASTATIN 10 ANALOG

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Page/Page column 47; 49, (2021/05/07)

Provided herein is a dolastatin 10 analog, useful for preparing conjugates thereof with targeting, diagnostic, imaging and other moieties. Also provided are the conjugates and uses thereof.

Bioreducible Poly- l -Lysine-Poly[HPMA] Block Copolymers Obtained by RAFT-Polymerization as Efficient Polyplex-Transfection Reagents

Tappertzhofen, Kristof,Beck, Simone,Montermann, Evelyn,Huesmann, David,Barz, Matthias,Koynov, Kaloian,Bros, Matthias,Zentel, Rudolf

, p. 106 - 120 (2016/01/25)

Polylysine-b-p[HPMA] block copolymers containing a redox-responsive disulfide bond between both blocks are synthesized by RAFT polymerization of pentafluorphenyl-methacrylate with a macro-CTA from N∈-benzyloxycarbonyl (Cbz) protected polylysine

TUNABLE FLUORESCENCE USING CLEAVABLE LINKERS

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Paragraph 0066-0067, (2014/11/11)

The invention relates to cleavable chemistry in general, and in particular, to tunable fluoresence using cleavable linkers present in fluorochrome-quencher conjugates.

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