Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Biochemical Engineering >  Biochemical Reagents >  Biological Dyes >  CELESTINE BLUE

CELESTINE BLUE

Basic information Safety Supplier Related

CELESTINE BLUE Basic information

Product Name:
CELESTINE BLUE
Synonyms:
  • CelestinBlueForMicroscopy
  • Celestine Blue, pure
  • Lapis lazuli blue
  • 1-(Aminocarbonyl)-7-(diethylamino)-3,4-dihydroxyphenoxazin-5-ium chloride
  • Coreine Blue B
  • Coreine RR No. 65
  • Gallo Sky Blue B
  • Gallo Sky Blue S
CAS:
1562-90-9
MF:
C17H18ClN3O4
MW:
363.8
EINECS:
216-346-2
Mol File:
1562-90-9.mol
More
Less

CELESTINE BLUE Chemical Properties

Melting point:
227-230 °C
form 
Powder
Colour Index 
51050
color 
Very dark brown to dark gray to black
Odor
Odorless
Merck 
13,1971
BRN 
3830911
InChIKey
VXAFJUDTZSMEFN-UHFFFAOYSA-N
CAS DataBase Reference
1562-90-9(CAS DataBase Reference)
More
Less

Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
22-24/25
WGK Germany 
3
HS Code 
32041200

MSDS

More
Less

CELESTINE BLUE Usage And Synthesis

Description

Coelestin Blue B 40, C.I. 51 050 [1562-90 9] is correspondingly obtained by action of 4 nitrosodiethylaniline hydrochloride with gallamide.

Chemical Properties

Black powder

Uses

Celestine Blue is a cationic dye used in cell staining. Dyes and metabolites.

Uses

To dye fabrics a navy-blue color with faint reddish tinge. As nuclear and connective tissue stain. One of the ingredients of Picro-Mallory stain: Lendrum, McFarlane, J. Pathol. Bacteriol. 50, 381 (1940).

Definition

ChEBI: Celestin blue B is an organic chloride salt composed of 1-carbamoyl-7-(diethylamino)-3,4-dihydroxyphenoxazin-5-ium and chloride ions in a 1:1 ratio. A histological dye used in solution with an iron alum mordant as a hematoxylin substitute in the H&E stain. It has a role as a fluorochrome and a histological dye. It contains a Celestin blue B(1+).

Preparation

excessive amounts of ?N,N-diethyl-4-nitrosobenzenamine or N,N-diethyl-4-(phenyldiazenyl)benzenamine?and 3,4,5-Trihydroxybenzamide reaction.

Synthesis

In an enamelled 6000 L ket tle equipped with a wooden gate stirrer, 110 kg of gallamide and 2000 L of alcohol (denatured, 94 %) are brought to a rapid boil. Over 10 h, 240 kg of nitrosodiethylaniline hydrochloride, dissolved in 1500 L of ethanol, is allowed to flow in. After addition of 21 kg of potassium carbonate, the reaction mixture is boiled for an other 1 h and allowed to cool to 20 ℃; 40 L of 20 % hydrochloric acid is added, and the mix ture is pressed into asuctionfilter withafiltering stone bottom. After stirring with 500 L of 20 % hydrochloric acid, the mixture is filtered under suction until the product is well dried, and the product is further dried at 70 ℃. Yield: 95 %. The ethanol is recovered by distillation.

Properties and Applications

red light navy blue. Soluble in water for red light purple, slightly soluble in ethanol for blue. In concentrated sulfuric acid for Daisy blue, dilution after magenta. Dye aqueous solution and sodium hydroxide as blue purple and blue precipitation.

Standard Ironing Fastness Light Fastness Fulling Persperation Fastness Soaping Water
Alkali Acid
ISO 5 5 3-4 5 4 3

CELESTINE BLUESupplier

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006608290; 18621169109
Email
market03@meryer.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Email
zhangsn@titansci.com
BEST-REAGENT
Tel
400-1166-196 18981987031
Email
cdhxsj@163.com