33203-82-6

Basic information

• Product Name: BASIC BLUE 3
• Synonyms: CI BASIC BLUE 3;CI 51004;CI 42775;CI NO 51004;BLEU LUMIERE;BLUE DE LYON;BASIC BLUE 3;SOLVENT BLUE 3
• CAS NO: 33203-82-6
• Molecular Formula: C₂₀H₂₆N₃O*Cl
• Molecular Weight: 359.89
• EINECS: 251-403-5
• Product Categories: Dyes and Pigments;B;Stains and Dyes;Stains&Dyes, A to
• Mol File: 33203-82-6.mol

Chemical Properties

• Melting Point: 205 °C (dec.)(lit.)
• Boiling Point: 475.7°C at 760 mmHg
• Flash Point: 241.5°C
• Appearance: /
• Density: 1.09g/cm³
• Vapor Pressure: 3.24E-09mmHg at 25°C
• Refractive Index: 1.575
• Storage Temp.: room temp
• CAS DataBase Reference: BASIC BLUE 3(CAS DataBase Reference)
• NIST Chemistry Reference: BASIC BLUE 3(33203-82-6)
• EPA Substance Registry System: BASIC BLUE 3(33203-82-6)

Safety Data

• Safety Statements: 22-24/25
• WGK Germany: 3
• Hazardous Substances Data: 33203-82-6(Hazardous Substances Data)

Usage

Uses

Used in Textile Industry:
BASIC BLUE 3 is used as a colorant for dyeing acrylic fabrics. Its properties include a green light blue shade, with a water solubility of 40 g/L at 20°C. The solubility is minimally affected by temperature changes, and the aqueous solution appears green light blue. When exposed to tungsten light, the color appears more green, while the presence of copper ions in the dyeing process significantly turns the color green, and the presence of iron ions darkens the shade.
Additionally, BASIC BLUE 3 is used for graft copolymerization dyeing of wool/nitriles and stick/acrylic blended fabrics. It can also be utilized for direct printing on acrylic carpets.
Standard:
The light fastness, perspiration fastness, ironing fastness, and soaping of BASIC BLUE 3 are rated according to ISO and AATCC standards. The ratings for light fastness, perspiration fastness, and ironing fastness range from 4 to 5, while the soaping rating is 4. The fading and staining ratings for BASIC BLUE 3 are also within the 4-5 range, indicating its durability and effectiveness as a dye.

Preparation

3-(Diethylamino)phenol or N,N-diethyl-3-methoxybenzenamine?nitrosation, then the product with hydrochloride between 3-(Diethylamino)phenol condensation.

Standard

Light Fastness

Fading

Stain

ISO

5

AATCC

4-5

InChI:InChI=1/C20H27N3O/c1-5-22(6-2)15-9-11-17-19(13-15)24-20-14-16(23(7-3)8-4)10-12-18(20)21-17/h9-15H,5-8H2,1-4H3

Upstream product

• 25912-14-5 2-amino-5-(diethylamino)phenol dihydrochloride 
• 91-68-9 3-diethylaminophenol 

Downstream Products

• 877669-17-5 3,7-bis(N,N-diethylamino)-10-(phenylthio)carbonylphenoxazine 
• 877669-19-7 3,7-bis-diethylamino-phenoxazine-10-carbothioic acid S-p-tolyl ester 
• 47367-75-9 N,N,N',N'-tetraethyloxonine 
• 37060-36-9 10-benzoyl-tetra-N-ethyl-10H-phenoxazine-3,7-diamine 
• 60-35-5 acetamide 
• 141-82-2 malonic acid 
• 499-75-2 carvacrol 
• 151-51-9 carbodiimide 
• 120-80-9 benzene-1,2-diol 
• 64-19-7 acetic acid 

Relevant articles and documents

A stable organic dye catholyte for long-life aqueous flow batteries

An organic dye, Basic blue 3 (BB3), was reported for the first time as a two-electron catholyte for aqueous redox flow batteries. The exceptional stability of BB3 enabled the full battery to achieve a high capacity retention of >99.991% per cycle during 1500 cycles.

Synthesis and antimalarial property of orally active phenoxazinium salts

Phenoxazinium salts were found to display good antimalarial efficacy in vivo against Plasmodium berghei. Several compounds provided 100% parasitemia clearance at a dose of 20-30 mg kg-1 x 4 days (ip) and good survival effects without obvious acute toxicity. They also showed excellent potency by oral administration. A preliminary pharmacokinetic study revealed that the oral availability of 1a was excellent.