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Details

Stereochemistry ACHIRAL
Molecular Formula C28H20N4O8S2
Molecular Weight 604.61
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 2
Charge 0

SHOW SMILES / InChI
Structure of 7-Hydroxy-8-[[4?-[(p-hydroxyphenyl)azo]-4-biphenylyl]azo]-1,3-naphthalenedisulfonic acid

SMILES

OC1=CC=C(C=C1)\N=N\C2=CC=C(C=C2)C3=CC=C(C=C3)\N=N\C4=C5C(=CC=C4O)C=C(C=C5S(O)(=O)=O)S(O)(=O)=O

InChI

InChIKey=GWPGBRYJVGKLHH-PNBBGTCESA-N
InChI=1S/C28H20N4O8S2/c33-23-12-10-22(11-13-23)30-29-20-6-1-17(2-7-20)18-3-8-21(9-4-18)31-32-28-25(34)14-5-19-15-24(41(35,36)37)16-26(27(19)28)42(38,39)40/h1-16,33-34H,(H,35,36,37)(H,38,39,40)/b30-29+,32-31+

HIDE SMILES / InChI

Molecular Formula C28H20N4O8S2
Molecular Weight 604.61
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 2
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Tue Apr 01 19:16:03 GMT 2025
Edited
by admin
on Tue Apr 01 19:16:03 GMT 2025
Record UNII
QZF62Z8HMM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
7-Hydroxy-8-[[4?-[(p-hydroxyphenyl)azo]-4-biphenylyl]azo]-1,3-naphthalenedisulfonic acid
Systematic Name English
1,3-Naphthalenedisulfonic acid, 7-hydroxy-8-[[4?-[(4-hydroxyphenyl)azo][1,1?-biphenyl]-4-yl]azo]-
Preferred Name English
7-Hydroxy-8-[2-[4?-[2-(4-hydroxyphenyl)diazenyl][1,1?-biphenyl]-4-yl]diazenyl]-1,3-naphthalenedisulfonic acid
Systematic Name English
1,3-Naphthalenedisulfonic acid, 7-hydroxy-8-[2-[4?-[2-(4-hydroxyphenyl)diazenyl][1,1?-biphenyl]-4-yl]diazenyl]-
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
204-184-5
Created by admin on Tue Apr 01 19:16:03 GMT 2025 , Edited by admin on Tue Apr 01 19:16:03 GMT 2025
PRIMARY
CAS
117-33-9
Created by admin on Tue Apr 01 19:16:03 GMT 2025 , Edited by admin on Tue Apr 01 19:16:03 GMT 2025
PRIMARY
FDA UNII
QZF62Z8HMM
Created by admin on Tue Apr 01 19:16:03 GMT 2025 , Edited by admin on Tue Apr 01 19:16:03 GMT 2025
PRIMARY
EPA CompTox
DTXSID5059452
Created by admin on Tue Apr 01 19:16:03 GMT 2025 , Edited by admin on Tue Apr 01 19:16:03 GMT 2025
PRIMARY