33229-34-4

Basic information

• Product Name: 2,2'-((4-((2-Hydroxyethyl)amino)-3-nitrophenyl)imino)bisethanol
• Synonyms: 2,2'-((4-((2-hydroxyethyl)amino)-3-nitrophenyl)imino)bisethanol;2,2'-[4-(2-HYDROXYETHYLAMINO)-3-NITROPHENYLIMINO]DIETHANOL;3-NITRO-4-[N-(2-ETHOXYL)AMINO]-N,N-DI(2-ETHOXYL)PHENYLAMINE;3-NITRO-4-[N-(2-HYDROXYETHYL)AMINO]-N,N-BIS(2-HYDROXYETHYL)ANILINE;HC BLUE 2;HC BLUE NO 2;JAROCOL BLUE 2;2,2’-((4-((2-hydroxyethyl)amino)-3-nitrophenyl)imino)bis-ethano
• CAS NO: 33229-34-4
• Molecular Formula: C₁₂H₁₉N₃O₅
• Molecular Weight: 285.3
• EINECS: 251-410-3
• Product Categories: Alkohols;Amino Alcohols;Organic Building Blocks;Oxygen Compounds;Amino Alcohols;Building Blocks;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds
• Mol File: 33229-34-4.mol
• Article Data: 1

Chemical Properties

• Melting Point: 108-111 °C(lit.)
• Boiling Point: 427.73°C (rough estimate)
• Flash Point: 306.2 °C
• Appearance: dark blue to dark brown microcrystalline powder
• Density: 1.2263 (rough estimate)
• Vapor Pressure: 0Pa at 25℃
• Refractive Index: 1.5600 (estimate)
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: water: soluble(lit.)
• PKA: 14.19±0.10(Predicted)
• Water Solubility: 4.57g/L at 25℃
• CAS DataBase Reference: 2,2'-((4-((2-Hydroxyethyl)amino)-3-nitrophenyl)imino)bisethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2'-((4-((2-Hydroxyethyl)amino)-3-nitrophenyl)imino)bisethanol(33229-34-4)
• EPA Substance Registry System: 2,2'-((4-((2-Hydroxyethyl)amino)-3-nitrophenyl)imino)bisethanol(33229-34-4)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 1
• RTECS: KL2880000
• Hazardous Substances Data: 33229-34-4(Hazardous Substances Data)

Usage

Description

2,2'-((4-((2-Hydroxyethyl)amino)-3-nitrophenyl)imino)bisethanol is a complex organic compound with a unique chemical structure that features a nitrophenyl imino group and two hydroxyethylamine moieties. 2,2'-((4-((2-Hydroxyethyl)amino)-3-nitrophenyl)imino)bisethanol has potential applications in various fields due to its chemical properties and reactivity.

Uses

Used in Hydrogel Applications:
2,2'-((4-((2-Hydroxyethyl)amino)-3-nitrophenyl)imino)bisethanol is used as a crosslinking agent for self-healing ureidopyrimidinone (UPy) hydrogels, specifically in poly(ethylene glycol) containing bifunctional UDP groups. Its incorporation enhances the visibility and self-healing properties of the hydrogel, making it suitable for various applications, such as soft materials, sensors, and drug delivery systems.
Used in Pharmaceutical Industry:
2,2'-((4-((2-Hydroxyethyl)amino)-3-nitrophenyl)imino)bisethanol may also be utilized in the pharmaceutical industry as a potential therapeutic agent or as a component in drug formulations. Its unique chemical structure allows for specific interactions with biological targets, which could lead to the development of new drugs or drug delivery systems.
Used in Chemical Synthesis:
In the field of chemical synthesis, 2,2'-((4-((2-Hydroxyethyl)amino)-3-nitrophenyl)imino)bisethanol can be employed as a building block or intermediate in the synthesis of more complex organic compounds. Its reactivity and functional groups make it a versatile component in the creation of novel molecules with potential applications in various industries.

Air & Water Reactions

May be sensitive to prolonged exposure to air. Slow oxidation. Insoluble in water.

Fire Hazard

Flash point data for 2,2'-((4-((2-Hydroxyethyl)amino)-3-nitrophenyl)imino)bisethanol are not available; however, 2,2'-((4-((2-Hydroxyethyl)amino)-3-nitrophenyl)imino)bisethanol is probably combustible.

Flammability and Explosibility

Nonflammable

Downstream Products

• 1313803-25-6 2-({4-[bis(2-hydroxyethyl)amino]-2-nitrophenyl}amino)ethyl[6-({[(6-isopropyl-4-oxo-1,4-dihydropyrimidin-2-yl)amino]carbonyl}amino)hexyl]carbamate 
• 29705-39-3 2-nitro-1-amino-4-[bis-(2-hydroxyethyl)-amino]-benzene 

Relevant articles and documents

4-Fluoro-3-nitro anilines

Compounds of formula: SPC1 Wherein W is EQU1 or EQU2 in which: (a) R4 and R5 are 5 identical or different and represent hydrogen, monovalent aliphatic, substituted or unsubstituted aryl, aralkyl and cycloalkyl, providing that not more than 1 of R4 or R5 is hydrogen, and (b) R3 is a divalent aliphatic radical.