10466-72-5

Basic information

• Product Name: N-(2,4-DINITROPHENYL)-6-AMINOHEXANOIC ACID
• Synonyms: 6-(2,4-DINITROPHENYL)AMINOHEXANOIC ACID;DNP-?-Aminocaproic acid 2,4-Dinitrophenyl-?-aminocaproic acid;N-2-4-dnp-epsilon-amino N-caproic acid*crystallin;N-2-4-DNP-EPSILON-AMINO N-CAPROIC ACID*C RYSTALLINE;n-(2,4-dinitrophenyl)-ε-amino-n-caproic acid;N-2,4-DNP-E-AMINO-N-CAPROICACID;6-N-(2,4-dinitrophenyl)aminohexanoic acid;N-2,4-dinitrophenyl-epsilon-amino-n-caproic acid
• CAS NO: 10466-72-5
• Molecular Formula: C₁₂H₁₅N₃O₆
• Molecular Weight: 297.26
• Mol File: 10466-72-5.mol
• Article Data: 3

Chemical Properties

• Melting Point: 133 °C
• Boiling Point: 532.5±50.0 °C(Predicted)
• Appearance: /
• Density: 1.417±0.06 g/cm3(Predicted)
• Refractive Index: 1.626
• Storage Temp.: −20°C
• PKA: 4.75±0.10(Predicted)
• CAS DataBase Reference: N-(2,4-DINITROPHENYL)-6-AMINOHEXANOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2,4-DINITROPHENYL)-6-AMINOHEXANOIC ACID(10466-72-5)
• EPA Substance Registry System: N-(2,4-DINITROPHENYL)-6-AMINOHEXANOIC ACID(10466-72-5)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 10466-72-5(Hazardous Substances Data)

Usage

Description

N-(2,4-DINITROPHENYL)-6-AMINOHEXANOIC ACID is a C-nitro compound that consists of hexanoic acid with a (2,4-dinitrophenyl)amino substituent at the C-6 position. It is a unique organic molecule with distinctive chemical properties that make it suitable for various applications, particularly in the field of analytical chemistry.

Uses

Used in Analytical Chemistry Industry:
N-(2,4-DINITROPHENYL)-6-AMINOHEXANOIC ACID is used as an analyte in microfluidic chips for the purpose of conducting chemical analyses and experiments. Its specific chemical structure allows it to be a valuable component in the development and functioning of microfluidic devices, which are miniature analytical systems that handle small volumes of fluids.
The use of N-(2,4-DINITROPHENYL)-6-AMINOHEXANOIC ACID in microfluidic chips enables researchers and scientists to perform high-throughput screening, detect trace amounts of substances, and carry out complex chemical reactions on a small scale. This contributes to advancements in fields such as drug discovery, diagnostics, and environmental monitoring, where precise and efficient analysis is crucial.

InChI:InChI=1/C18H19N3O6/c1-2-12(13-7-3-5-9-15(13)20(24)25)11-18(19,17(22)23)14-8-4-6-10-16(14)21(26)27/h3-10,12H,2,11,19H2,1H3,(H,22,23)

Upstream product

• 70-34-8 2,4-Dinitrofluorobenzene 
• 60-32-2 6-aminohexanoic acid 
• 616-06-8 2-amino-hexanoic acid 
• 97-00-7 1-chloro-2,4-dinitro-benzene 
• 1926-80-3 methyl 6-aminocaproate hydrochloride 
• 72007-89-7 6-(2,4-dinitro-anilino)-hexanoic acid methyl ester 

Downstream Products

• 82321-04-8 6-(2,4-dinitrophenylamino)hexanoic acid N-hydroxysuccinimide ester 
• 166321-87-5 (S)-2-{(S)-4-tert-Butoxycarbonyl-2-[6-(2,4-dinitro-phenylamino)-hexanoylamino]-butyrylamino}-pentanedioic acid di-tert-butyl ester 

Relevant articles and documents

Synthesis of DNP-modified GM3-based anticancer vaccine and evaluation of its immunological activities for cancer immunotherapy

Tumor-associated carbohydrate antigens (TACAs) are attractive targets for vaccine development. In this context, we described a strategy combining artificial TACA and glycoengineering for cancer vaccine development. A 2,4-ditrophenyl (DNP)-modified GM3 int

Pharmacokinetic studies with 3H-labelled synthetic antifibrinolytics

In rabbits and rats pharmacokinetic studies on the anti-fibrinolytics 4-aminomethylbenzoic acid (PAMBA), trans-4-aminomethylcyclohexane-1-carboxylic acid (AMCA), and epsilon-aminocaproic acid (EACA) were carried out using the tritium labelled compounds. F