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Home/Compounds/Research Reagent/1,6-naphthalenediol
C10H8O2
160.17 g/mol
Research ReagentWarning

1,6-Dihydroxynaphthalene

CAS575-44-0EC209-386-7
Category
Research Reagent
Compound Class
Alcohol
Primary Use
Research Compound

1,6-Dihydroxynaphthalene is one of the ten isomeric dihydroxynaphthalenes, consisting of a naphthalene ring with two hydroxyl substituents. It is primarily used as a research compound in chemical and laboratory settings.

research compoundlaboratory reagent

Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.

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Related Compounds

ReferenceSame Category

2-Methylthio-4-pyrimidinol

CAS5751-20-2

research compound

ReferenceSame Category

Ethyl thiophene-3-carboxylate

CAS5751-80-4

research compound

ReferenceSame Category

3,6-Dihydroxy-4,5-dimethylpyridazine

CAS5754-17-6

research compound

ReferenceSame Category

3,6-Dihydroxy-4-methylpyridazine

CAS5754-18-7

research compound

Safety Reference

Harmful
Harmful
Warning
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation

Customs Tariff Classification

The international HS code for 1,6-Dihydroxynaphthalene (CAS 575-44-0) is 2907.29.

HS code (international, 6-digit)

2907.29

EU CN code (8-digit)

2907 29 00

Classification per the EU customs inventory ECICS (2026-07 snapshot, HS 2022). National tariff lines and product form can affect the final classification.

Identifiers
IUPAC Name

naphthalene-1,6-diol

InChIKey

FZZQNEVOYIYFPF-UHFFFAOYSA-N

SMILES

C1=CC2=C(C=CC(=C2)O)C(=C1)O

Synonyms (13)
  • DIN
  • 1,6-Dihydroxynaphtalene
  • 1,6-Dihydroxynaphthalene
  • 1,6-Naphthalenediol
  • 1,6-Naphthalenediol (8CI,9CI)
  • 1,6-Naphthalindiol
  • 1,6-dihydroxyl naphthalene
  • 2,5-Dihydroxynaphthalene
  • 2,5-Naphthalenediol
  • 6-Hydroxy-1-naphthol
  • Naphthalene, 1,6-dihydroxy-
  • Naphthalene,6-dihydroxy-
  • naphthalene-1,6-diol

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