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1326-66-5

1326-66-5 Structure

1326-66-5 Structure
IdentificationBack Directory
[Name]

Sulphur yellow 2
[CAS]

1326-66-5
[Synonyms]

C.I. 53120
Eclipse Yellow G
Sulphur yellow 2
Light Yellow GC
Diresul Yellow MS
Sulphur Yellow GR.
Calcogene Yellow S-CF
Sulfur Light Yellow GC
Sulphur Light Yellow GC
Acco Sulfur Yellow S-CF
Dycosulphur Light Yellow GC
Sulfur yellow 2 (C.I. 53120)
Formamide, N,N'-(4-methyl-1,3-phenylene)bis-, reaction products with [1,1'-biphenyl]-4,4'-diamine and sulfur
[EINECS(EC#)]

215-437-4
[MOL File]

1326-66-5.mol
Chemical PropertiesBack Directory
[CAS DataBase Reference]

1326-66-5
Raw materials And Preparation ProductsBack Directory
[Raw materials]

2,4-Diaminotoluene-->FENURON-->Benzidine-->4-methyl-N,N'-m-phenylenediformamide-->Bromocresol green
Hazard InformationBack Directory
[Chemical Properties]

Yellow-brown powder. Insoluble in water, but brownish-yellow in sodium sulfide solution. Partially soluble in concentrated sulfuric acid, producing a yellow precipitate upon dilution. Slightly discolors in alkaline hydrosulfite solution, completely fades in sodium hypochlorite, and turns dark orange in concentrated sulfuric acid.
[Uses]

Sulphur yellow 2 is mainly used for dyeing cotton, linen, viscose fibers, and vinylon, and also for leather coloring. It can be used for color mixing, producing shades such as grass green, beige, ginger yellow, yellowish brown, dark brown, dark green, and dark gray.
[Definition]

ChEBI: Cyclooctasulfur is a homomonocyclic compound composed of eight sulfur atoms. It has been isolated from Ganoderma lucidum, a mushroom commonly used in Chinese medicine. It has a role as a fungal metabolite and a bacterial metabolite. It is an elemental sulfur and a homomonocyclic compound.
[Properties and Applications]

Standard

Acid Resistance

Alkali Resistance

Light Fastness

Fulling

Persperation Fastness

Soaping

Moderate

Severe

ISO

3-4

4

2

4

4-5

4

3

AATCC

4

5

3

2

2

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