chempirical

Acid red 88

C20H13N2NaO4SCAS 1658-56-6400.38 g/mol

Open in Covalent MOL file
O−SOONNHONa+
AzoPhenolSulfonic acid

Properties

Molecular formula
C20H13N2NaO4S
Molar mass
400.38 g/mol
Exact mass
400.0494 Da
logP
4.98Crippen estimate
Polar surface area
99.3 Ų
H-bond donors / acceptors
2 / 5
Rotatable bonds
3

Hazards

No GHS classification is on file for this compound. That is not evidence that it is harmless. Search the SDS library

Identifiers

CAS number
1658-56-6
SMILES
[O-]S(=O)(=O)c1ccc(N=Nc2c(O)ccc3ccccc23)c2ccccc12.[Na+]

The InChI we hold for this record describes the parent acid and the metal separately rather than the salt above, so it is not shown here.

Weigh it out

Type any one amount. The others follow from the molar mass.

Names and synonyms

109 names · show all
  • Acid scarlet G
  • 1-Naphthalenesulfonic acid, 4-[2-(2-hydroxy-1-naphthalenyl)diazenyl]-, sodium salt (1:1)
  • Naphthalene red J
  • 1-Naphthalenesulfonic acid, 4-[(2-hydroxy-1-naphthalenyl)azo]-, monosodium salt
  • C.I. Acid Red 88, monosodium salt
  • 11391 Red
  • C.I. 15620
  • Acid cardinal G
  • Acid leather red ROC
  • Acid red AV
  • Acid rose AV
  • Airedale red A
  • Amacid fast red A
  • Anthrosin BRX
  • Atul acid fast red A
  • Azo acid red GS
  • Benzyl red S
  • Benzyl red ROC
  • Brasilan red S
  • Bucacid fast red A
  • Calcocid fast red A
  • Colacid red AV
  • Dai-ei Roccelline
  • Diacid red A
  • Eniacid fast red A
  • Eriosin roccelline
  • Eriosin roccelline SS
  • Fast acid red G
  • Fast red A
  • Fast red S
  • Fast red AE
  • Fast red AG
  • Fast red ALS
  • Fast red AV
  • Fast red MA
  • Fenazo red M
  • Hidacid fast red A
  • Hispacid fast red A
  • Kayaku roccelline
  • Lurazol red E
  • 2-Naphthol red J
  • Naphtocard fast red C
  • Neklacid fast red A
  • Neutral red R
  • New red WO
  • Nitto roccelline
  • Peony
  • Plastoresin red RC
  • Pontacyl fast red AS
  • Red J
  • Rocceline
  • Roccelline
  • Roccelline A
  • Roccelline B
  • Roccelline KG
  • Roccelline NS
  • Roccelline G
  • Roccelline K
  • Roccelline L
  • Roccelline S
  • Shikiso roccelline
  • Tertracid red RO
  • Toyo roccelline
  • Vondacid red GN
  • C.I. Acid red 88
  • Ext D and C red no. 8
  • Red no. 506
  • Fast Red A (acid dye)
  • Naphthalene red JS
  • Acid red G
  • Rocelline
  • Basacid red 340
  • Japan red no. 506
  • Japan red 506
  • Sodium 4-[(2-hydroxy-1-naphthyl)azo]-1-naphthalene sulfonate
  • Roccelline NS 200
  • Acid fast red A
  • Acid red A (chinese)
  • Colocid fast red A
  • Romexal red AV
  • Libacid fast red A
  • Monacid red A
  • Dyacid red J
  • Triacid fast red av
  • Ritacid rosalin AV
  • Triacid red an
  • Dycosacid red A
  • Derma fur red R 150
  • Dinacid fast red A
  • Multacid red A
  • Fur red KB
  • Multicuer red A
  • Daedo acid roccelline NS
  • Apollo acid rocceline
  • Anadurm red A-ROC
  • Fabracid red S-A
  • Ichoacid red A
  • Acid red A
  • Indacid acid red A
  • Vopsider red AAV
  • Rifa acid roccelline NS
  • Ambicid fast red E
  • Conacid red MM
  • Vicoacid fast red A
  • Sandal acid red G
  • Rifa leather red E
  • Cavalene red A
  • Kemacid fast red A
  • Red for furs G

Work with Acid red 88

Predict the NMR spectrum1H and 13C shifts with multiplicities Make a solutionWhat to weigh for any molarity and volume Check drug-likenessLipinski, Veber and lead-likeness Isotope patternExact mass and the mass spectrum pattern

Similar compounds

Acid brown M5850-16-877 % similar C.I. Mordant black 172538-85-475 % similar Ponceau 4R2611-82-772 % similar Pigment red 49:11103-38-467 % similar C.I. Acid red 9710169-02-566 % similar Acid orange 7633-96-565 % similar Amaranth (dye)915-67-364 % similar Azorubine3567-69-961 % similar

Tanimoto similarity of circular fingerprints over the whole catalogue. All similar compounds

Elsewhere

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