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1,6-Dihydroxynaphthalene

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Company Name: Macheng jinxin biotechnology co., LTD  Gold
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Company Name: Shanghai TongYuan Chemical Co., Ltd.  Gold
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1,6-Dihydroxynaphthalene manufacturers

1,6-Dihydroxynaphthalene Basic information
Product Name:1,6-Dihydroxynaphthalene
Synonyms:1,6-DIHYDROXYNAPHTHALENE;2,5-DIHYDROXYNAPHTHALENE;2,5-Naphthalenediol;6-Hydroxy-1-naphthol;C.I. 76630;c.i.76630;Naphthalene, 1,6-dihydroxy-;1,6-Dihydroxynaphtalene
CAS:575-44-0
MF:C10H8O2
MW:160.17
EINECS:209-386-7
Product Categories:API intermediates;Naphthalene derivatives;Intermediates of Dyes and Pigments;FINE Chemical & INTERMEDIATES;bc0001
Mol File:575-44-0.mol
1,6-Dihydroxynaphthalene Structure
1,6-Dihydroxynaphthalene Chemical Properties
Melting point 130-133 °C (lit.)
Boiling point 246.06°C (rough estimate)
density 1.0924 (rough estimate)
refractive index 1.5418 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility very faint turbidity in Methanol
form Powder or Crystalline Powder
pka9.26±0.40(Predicted)
color White to brown
BRN 1939032
InChIInChI=1S/C10H8O2/c11-8-4-5-9-7(6-8)2-1-3-10(9)12/h1-6,11-12H
InChIKeyFZZQNEVOYIYFPF-UHFFFAOYSA-N
SMILESC1(O)=C2C(C=C(O)C=C2)=CC=C1
CAS DataBase Reference575-44-0(CAS DataBase Reference)
NIST Chemistry Reference1,6-Naphthalenediol(575-44-0)
EPA Substance Registry System1,6-Naphthalenediol (575-44-0)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 2
RTECS QJ4743333
TSCA TSCA listed
HS Code 29072990
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
1,6-Dihydroxynaphthalene English
SigmaAldrich English
ALFA English
1,6-Dihydroxynaphthalene Usage And Synthesis
Chemical PropertiesBeige powder
Uses1,6-Dihydroxynaphthalene is used as a dye and pharmaceutical intermediate.
DefinitionChEBI: Naphthalene-1,6-diol is a naphthalenediol.
Synthesis1,6-Naphthalenediol [575-44-0], mp 138℃, is synthesized by caustic fusion of naphthalene1,6-disulfonic acid at 330 C. It couples with diazotized anilines to form disazo and trisazo derivatives.
Purification MethodsCrystallise it from *benzene or *benzene/EtOH after treatment with charcoal. [Beilstein 6 IV 6557.]
1,6-Dihydroxynaphthalene Preparation Products And Raw materials
Preparation Products9-Diethylamino-2-hydroxy-5H-benz(a)--->2,5-Dimethoxynaphthalene-->2-(11-Hydroxy-3-oxo-3H-dibenzo[c,h]xanthen-7-yl)benzoic acid
Tag:1,6-Dihydroxynaphthalene(575-44-0) Related Product Information
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