Acid Red 154

Acid Red 154

Acid Red 154

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0 Metric Ton

Negotiable

  • Min.Order :0 Metric Ton
  • Purity: 99
  • Payment Terms : T/T

Keywords

Follone Red 3BW C.I. Acid Red 154 AcidViolet Red B

Quick Details

  • Appearance:
  • Application:The Acid Red 154 with cas registry number of 6507-79-5 belongs to the categories of organics. It is also known as 3,3'-(Cyclohexylidenebis((2-methyl-4,1-phenylene)azo))bis(4,6-dihydroxy-2-naphthalenes
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  • Transportation:The Acid Red 154 with cas registry number of 6507-79-5 belongs to the categories of organics. It is also known as 3,3'-(Cyclohexylidenebis((2-methyl-4,1-phenylene)azo))bis(4,6-dihydroxy-2-naphthalenes

Superiority:

The Acid Red 154 with cas registry number of 6507-79-5 belongs to the categories of organics. It is also known as 3,3'-(Cyclohexylidenebis((2-methyl-4,1-phenylene)azo))bis(4,6-dihydroxy-2-naphthalenesulfonic acid), disodium salt. This chemical also has other registry number which is 53988-76-4. Its EINECS registry number is 229-398-6. Its systematic name is 2-Naphthalenesulfonic acid, 3,3'-(cyclohexylidenebis((2-methyl-4,1-phenylene)azo))bis(4,6-dihydroxy-, disodium salt. And its IUPAC name is called disodium 3-[2-[4-[1-[4-[2-(1,7-dioxo-3-sulfonatonaphthalen-2-yl)hydrazinyl]-3-methylphenyl]cyclohexyl]-2-methylphenyl]hydrazinyl]-4,6-dioxonaphthalene-2-sulfonate.

This chemical is deep purple powder. It is soluble in water with appearance of magenta. After adding concentrated hydrochloric acid, the solution shows wine red. When adding concentrated sodium hydroxide, the solution will show maroon. It is slightly soluble in ethanol and shows magenta. This chemical is mainly used for nylon, silk and wool dyeing and for paper, leather and casein plastics coloring.

Physical properties about this chemical are: (1)#H bond acceptors: 14; (2)#H bond donors: 6; (3)#Freely Rotating Bonds: 12; (4)Polar Surface Area: 261.52 Å2.

You can still convert the following datas into molecular structure:
(1)InChI: InChI=1/C40H36N4O10S2.2Na/c1-22-16-26(8-12-32(22)41-43-36-34(55(49,50)51)18-24-6-10-28(45)20-30(24)38(36)47)40(14-4-3-5-15-40)27-9-13-33(23(2)17-27)42-44-37-35(56(52,53)54)19-25-7-11-29(46)21-31(25)39(37)48;;/h6-13,16-21,45-48H,3-5,14-15H2,1-2H3,(H,49,50,51)(H,52,53,54);;/q;2*+1/p-2/b43-41+,44-42+;; 
(2)Smiles: [Na+].[Na+].C1(CCCCC1)(c1cc(c(cc1)\N=N\c1c(cc2ccc(cc2c1O)O)S(=O)(=O)[O-])C)c1cc(c(cc1)\N=N\c1c(cc2ccc(cc2c1O)O)S(=O)(=O)[O-])C

Details:

The Acid Red 154 with cas registry number of 6507-79-5 belongs to the categories of organics. It is also known as 3,3'-(Cyclohexylidenebis((2-methyl-4,1-phenylene)azo))bis(4,6-dihydroxy-2-naphthalenesulfonic acid), disodium salt. This chemical also has other registry number which is 53988-76-4. Its EINECS registry number is 229-398-6. Its systematic name is 2-Naphthalenesulfonic acid, 3,3'-(cyclohexylidenebis((2-methyl-4,1-phenylene)azo))bis(4,6-dihydroxy-, disodium salt. And its IUPAC name is called disodium 3-[2-[4-[1-[4-[2-(1,7-dioxo-3-sulfonatonaphthalen-2-yl)hydrazinyl]-3-methylphenyl]cyclohexyl]-2-methylphenyl]hydrazinyl]-4,6-dioxonaphthalene-2-sulfonate.

This chemical is deep purple powder. It is soluble in water with appearance of magenta. After adding concentrated hydrochloric acid, the solution shows wine red. When adding concentrated sodium hydroxide, the solution will show maroon. It is slightly soluble in ethanol and shows magenta. This chemical is mainly used for nylon, silk and wool dyeing and for paper, leather and casein plastics coloring.

Physical properties about this chemical are: (1)#H bond acceptors: 14; (2)#H bond donors: 6; (3)#Freely Rotating Bonds: 12; (4)Polar Surface Area: 261.52 Å2.

You can still convert the following datas into molecular structure:
(1)InChI: InChI=1/C40H36N4O10S2.2Na/c1-22-16-26(8-12-32(22)41-43-36-34(55(49,50)51)18-24-6-10-28(45)20-30(24)38(36)47)40(14-4-3-5-15-40)27-9-13-33(23(2)17-27)42-44-37-35(56(52,53)54)19-25-7-11-29(46)21-31(25)39(37)48;;/h6-13,16-21,45-48H,3-5,14-15H2,1-2H3,(H,49,50,51)(H,52,53,54);;/q;2*+1/p-2/b43-41+,44-42+;; 
(2)Smiles: [Na+].[Na+].C1(CCCCC1)(c1cc(c(cc1)\N=N\c1c(cc2ccc(cc2c1O)O)S(=O)(=O)[O-])C)c1cc(c(cc1)\N=N\c1c(cc2ccc(cc2c1O)O)S(=O)(=O)[O-])C

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