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INDIGOTINE,China price supplier

INDIGOTINE
min.order / fob price
≥1 piece
OriginChina
Production Capacity
CategoryColorant
Update Time2025-12-19
company profile
Shanghai United Chemical Co., Limited
China
Contact: Ms.Belinda Gao
Tel: 86-21-28748889
Number of Employees: < 20
Business Type: Manufacture & Trade
product details
Model No:UC-6010
Origin:China

 

SYNONYMS

CI Food Blue 1, FD&C Blue No. 2, Indigo Carmine, CI (1975) No. 73015, INS No. 132

DEFINITION

Consists essentially of a mixture of disodium 3,3' -dioxo-[delta 2,2' -biindoline]-5,5'-disulfonate, and disodium 3,3'-dioxo-[delta 2,2' -biindoline]-5,7'-disulfonate and subsidiary colouring matters together with sodium chloride and/or sodium sulfate as the principal uncoloured components.

May be converted to the corresponding aluminium lake in which case only the General Specifications for Aluminium Lakes of Colouring Matters apply.

Chemical names

Disodium 3,3'-dioxo-[delta 2,2' -biindoline]-5,5'-disulfonate

C.A.S. number

860-22-0 (5,5' isomer)

Chemical formula

C 16 H 8 N 2 Na 2 O 8 S 2

Structural formula

Formula weight

466.36

Assay

Not less than 85% total colouring matters.

Not more than 18% of disodium 3,3'-dioxo-[delta 2,2' -biindoline]-5,7'-disulfonate

DESCRIPTION

Blue powder or granules

FUNCTIONAL USES

Colour

CHARACTERISTICS

IDENTIFICATION

Solubility (Vol. 4)

Soluble in water; sparingly soluble in ethanol

Identification of colouring matters (Vol. 4)

Passes test

PURITY


 

Loss on drying at 135o

Not more than 15% together with chloride and sulfate calculated as sodium salts

Water insoluble matter

(Vol. 4)

Not more than 0.2%

Lead (Vol. 4)

Not more than 2 mg/kg

Determine using an atomic absorption technique appropriate to the specified level. The selection of sample size and method of sample preparation may be based on the principles of the method described in Volume 4, ¡°Instrumental Methods.¡±

Subsidiary colouring matters (Vol. 4)

Not more than 1% (except disodium 3,3'-dioxo-[delta 2,2' -biindoline]- 5,7'-disulfonate)

Use the following conditions:

Developing solvent: No. 3

Height of ascent of solvent front: approximately 17 cm

Note 1. The 5,7' isomer is separated as a wide blue zone just in front of the main blue band. Do not include this zone in the subsidiary colouring matter zones which are cut out and measured.

Note 2. The 15 ml sodium hydrogen carbonate solution used in the general procedure is replaced by 15 ml 0.05 N hydrochloric acid in order to avoid the decomposition which the sulfonated indigo undergoes in alkaline solution.

organic compounds other than colouring matters

(Vol. 4)

Not more than 0.5% of sum of isatin-5-sulfonic acid, 5-sulfoanthranilic acid and anthranilic acid

Use liquid chromatography under the following conditions:

HPLC elution gradient: 2 to 100% gradient followed by elution at 100%

Unsulfonated primary aromatic amines (Vol. 4)

Not more than 0.01% calculated as aniline

Ether extractable matter (Vol. 4)

Not more than 0.2%

Weigh accurately about 2 g sample instead of the 5 g stated in the general methods

METHOD OF

ASSAY

Proceed as directed under Total Content by Titration with Titanous Chloride in Volume 4, using the following:

Weight of sample: 1.0-1.1 g

Buffer: 15 g sodium hydrogen tartrate

Weight (D) of colouring matters equivalent to 1.00 ml of 0.1 N TiCl 3 : 0.02332 g

Isomer content by paper chromatography

Refer to the conditions for the determination of subsidiary colouring matters (above). Cut the isomer band from the chromatogram in the manner detailed for the subsidiary bands, extract into solvent and measure the absorbance at its Smax. Measure the absorbance of the corresponding blank at the same wavelength. As a standard use 0.1 ml of an 0.20% solution of the sample applied to the 18 cm x 0.7 cm rectangle.


 

Isomer expressed as a percentage of the sample =

[A/As] x 20% x [D/100]

where A and As are the net absorbances of the isomer and standard, respectively, and D is the total colouring matters content of the sample.

Isomer content by HPLC

The 5,7' isomer separates under the HPLC conditions detailed above for the separation of subsidiary colouring matters, and the amount present can be quantified.

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