Primuline - Dye content ≥50% , CAS No.8064-60-6

CAS: 8064-60-6 Cat. No.: P304698 Molecular Weight: 475.54 PubChem CID: 415713

GRADE & PURITY Dye content ≥50%

Synonyms

D91982 | Primulin fluorochrome | (2,6':2',6''-Terbenzothiazole)-7-sulfonic acid, 2''-(4-aminophenyl)-6-methyl-, monosodium salt, mixt. with 2'-(4-aminophenyl)-6-methyl(2,6-bibenzothiazole)-7-sulfonic acid monosodium salt | C.I. Direct Yellow 7, sodium sal

Storage

Room temperature

Shipped In

Normal

Specifications

Synonyms

D91982 | Primulin fluorochrome | (2, 6':2', 6''-Terbenzothiazole)-7-sulfonic acid, 2''-(4-aminophenyl)-6-methyl-, monosodium salt, mixt. with 2'-(4-aminophenyl)-6-methyl(2, 6-bibenzothiazole)-7-sulfonic acid monosodium salt | C.I. Direct Yellow 7, sodium sal

Specifications & Purity

Dye content ≥50%

Biochemical and Physiological Mechanisms

Primrose yellow, also known as direct yellow 59 or primroselin, is a more sensitive and non-destructive lipid dye. It is widely used as a fluorescent dye in preparative thin layer chromatography (TLC). Primrose yellow is suitable for in vivo staining. It

Storage

Room temperature

Shipped In

Normal

Names and Identifiers

• Pubchem Sid: 488189700
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488189700
• Canonical Smiles: CC1=C(C2=C(C=C1)N=C(S2)C3=CC4=C(C=C3)N=C(S4)C5=CC=C(C=C5)N)S(=O)(=O)O.CC1=C(C2=C(C=C1)N=C(S2)C3=CC4=C(C=C3)N=C(S4)C5=CC6=C(C=C5)N=C(S6)C7=CC=C(C=C7)N)S(=O)(=O)O
• IUPAC Name: 2-[2-[2-(4-aminophenyl)-1,3-benzothiazol-6-yl]-1,3-benzothiazol-6-yl]-6-methyl-1,3-benzothiazole-7-sulfonic acid;2-[2-(4-aminophenyl)-1,3-benzothiazol-6-yl]-6-methyl-1,3-benzothiazole-7-sulfonic acid
• InChIKey: ZAXBCXVACRXRQZ-UHFFFAOYSA-N
• INCHI: 1S/C28H18N4O3S4.C21H15N3O3S3/c1-14-2-9-21-24(25(14)39(33,34)35)38-28(32-21)17-6-11-20-23(13-17)37-27(31-20)16-5-10-19-22(12-16)36-26(30-19)15-3-7-18(29)8-4-15;1-11-2-8-16-18(19(11)30(25,26)27)29-21(24-16)13-5-9-15-17(10-13)28-20(23-15)12-3-6-14(22)7-4-12/h2-13H,29H2,1H3,(H,33,34,35);2-10H,22H2,1H3,(H,25,26,27)
• Isomeric SMILES: CC1=C(C2=C(C=C1)N=C(S2)C3=CC4=C(C=C3)N=C(S4)C5=CC=C(C=C5)N)S(=O)(=O)O.CC1=C(C2=C(C=C1)N=C(S2)C3=CC4=C(C=C3)N=C(S4)C5=CC6=C(C=C5)N=C(S6)C7=CC=C(C=C7)N)S(=O)(=O)O
• PubChem CID: 415713
• Molecular Weight: 475.54

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Benzothiazoles

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Benzothiazoles
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzothiazoles
• Alternative Parents: Arylsulfonic acids and derivatives Aniline and substituted anilines Thiazoles Sulfonyls Organosulfonic acids Heteroaromatic compounds Azacyclic compounds Primary amines Organopnictogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Not available
• Substituents: Arylsulfonic acid or derivatives - 1,3-benzothiazole - Aniline or substituted anilines - Monocyclic benzene moiety - Benzenoid - Azole - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organosulfonic acid - Sulfonyl - Thiazole - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Primary amine - Organosulfur compound - Amine - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as benzothiazoles. These are organic compounds containing a benzene fused to a thiazole ring (a five-membered ring with four carbon atoms, one nitrogen atom and one sulfur atom).
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y