ChemicalBook > CAS DataBase List > 2,3-Dihydroxynaphthalene

2,3-Dihydroxynaphthalene

Product Name
2,3-Dihydroxynaphthalene
CAS No.
92-44-4
Chemical Name
2,3-Dihydroxynaphthalene
Synonyms
Naphthalene-2,3-diol;2,3-Dihydroxy;2,3-DIHYDROXYNAPHTHALENE, SUBL.;2,3-NAPHTHALENEDIOL;Naphthalin-2,3-diol;Dihydroxynaphthalene;Naphthalenediol-(2,3);3-Dihydroxynaphthalene;2,3-Dihydroxynapthalene;2,3-DIHYDROXYNAPHTHALENE
CBNumber
CB8736136
Molecular Formula
C10H8O2
Formula Weight
160.17
MOL File
92-44-4.mol
More
Less

2,3-Dihydroxynaphthalene Property

Melting point:
161-165 °C (lit.) 162-164 °C
Boiling point:
246.06°C (rough estimate)
Density 
1.0924 (rough estimate)
vapor pressure 
0.8 hPa (149 °C)
refractive index 
1.5178 (estimate)
Flash point:
175 °C
storage temp. 
Store below +30°C.
solubility 
4g/l
form 
Powder
pka
9.10±0.40(Predicted)
color 
White to pinkish to beige-grayish
PH
6 (1g/l, H2O, 20℃)
Water Solubility 
slightly soluble
BRN 
742375
CAS DataBase Reference
92-44-4(CAS DataBase Reference)
NIST Chemistry Reference
2,3-Naphthalenediol(92-44-4)
EPA Substance Registry System
2,3-Naphthalenediol (92-44-4)
More
Less

Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
RTECS 
QJ4750000
10-23
Autoignition Temperature
>330 °C
TSCA 
Yes
HS Code 
29072900
Toxicity
LD50 orally in Rabbit: 970 mg/kg
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H302Harmful if swallowed

H318Causes serious eye damage

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P501Dispose of contents/container to..…

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
8.14578
Product name
2,3-Naphthalenediol
Purity
for synthesis
Packaging
50g
Price
$101
Updated
2024/03/01
Sigma-Aldrich
Product number
37760
Product name
2,3-Dihydroxynaphthalene
Purity
≥98.0% (HPLC)
Packaging
50g
Price
$147
Updated
2024/03/01
Sigma-Aldrich
Product number
37760
Product name
2,3-Dihydroxynaphthalene
Purity
≥98.0% (HPLC)
Packaging
250g
Price
$228
Updated
2024/03/01
TCI Chemical
Product number
D0593
Product name
2,3-Dihydroxynaphthalene
Purity
>98.0%(GC)(T)
Packaging
25g
Price
$40
Updated
2024/03/01
TCI Chemical
Product number
D0593
Product name
2,3-Dihydroxynaphthalene
Purity
>98.0%(GC)(T)
Packaging
250g
Price
$258
Updated
2024/03/01
More
Less

2,3-Dihydroxynaphthalene Chemical Properties,Usage,Production

Chemical Properties

Off white to redish white powder. 2,3-Naphthalenediol [92-44-4], mp 161℃, gives a dark blue color with iron(III) chloride; is aminated to 2- amino-3-naphthol at 140℃ and 2,3-naphthalenediamine at 240℃; and couples with diazotized anilines in the 1- or 1,4-positions.

Uses

2,3-Naphthalenediol is used in cosmetics asa component of oxidative hair dye. It is usedat a concentration of <0.1%.

Uses

2,3-Dihydroxynaphthalene is used in making dyes, pigments, fluorescent whiteners, tanning agents, antioxidants, and antiseptics.

Uses

2,3-Dihydroxynaphthalene may be used in the following studies:

  • Construction of dinaphtho[2,1-b;2′,3′-d]furan-6-ol, via dehydration reaction in the presence of strong acid.
  • As fused ring catecholate type ligand for the surface modification of nanocrystalline TiO2 particles.
  • As adsorptive and competing ligand during the chemical speciation of iron in seawater by cathodic stripping voltammetry.
  • Synthesis of cyclotriphosphazene derivatives, used as non-halogen flame retardants

Definition

ChEBI: Naphthalene-2,3-diol is a naphthalenediol.

General Description

2,3-Dihydroxynaphthalene is a polyhydroxy phenol. It is an aromatic dihydroxy compound having hydroxyl groups at ortho positions. Its reaction with molybdenum(VI) complexes has been reported. The asymmetric oxidative coupling polymerization of 2,3-dihydroxynaphthalene using the Cu(I)-bisoxazoline complex as catalyst has been reported to afford poly(2,3-dihydroxy-1,4-naphthylene), having a continuous 1,1′-bi-2-naphthol main chain structure. The nitrodisplacement reaction between nitrophthalodinitriles and 2,3-dihydroxynaphthalene has been investigated.

Health Hazard

2,3-Naphthalenediol shows low toxicity andmild irritant actions on the skin and eyes. Theoral LD50 value for rats of a 5% solutionin propylene glycol may be on the orderof 675 mg/kg (calculated by the method ofWeil). The intravenous LD50 value for miceis 56 mg/kg. At 1% concentration, it causedslight eye irritation in female albino rabbitsand exhibited erythemal response in guineapigs. At the 0.1% level (concentration in hairdye), it had no reaction on human skin. Thiscompound was nonmutagenic in Salmonellatyphimurium strain tests.
There is very little information in the literatureon the toxicity of 2,3-naphthalenediol.Assessment by the CIR expert panel on thesafety of this compound as used in cosmeticshas been inconclusive (Cosmetic, Toiletryand Fragrance Association 1987b).

Synthesis

2,3-Dihydroxynaphthalene is prepared by caustic fusion of 3-hydroxynaphthalene-2,6-disulfonic acid followed by treatment with dilute sulfuric acid under pressure, or by acid desulfonation of 2,3-dihydroxynaphthalene-6-sulfonic acid.

2,3-Dihydroxynaphthalene Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

2,3-Dihydroxynaphthalene Suppliers

Ark Pharm, Inc.
Tel
847-367-3680
Fax
847-367-3681
Email
sales@arkpharminc.com
Country
United States
ProdList
1670
Advantage
56
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
Aston Chemical
Tel
13000000000
Email
sales@astonchem.com
Country
United States
ProdList
1634
Advantage
58
TCI America, Inc. (Tokyo Chemical Industry Co., Ltd.)
Tel
--
Fax
--
Email
.Crew@tcichemicals.com
Country
United States
ProdList
3164
Advantage
58
Fluorochem Ltd.
Tel
--
Fax
--
Email
enquiries@fluorochem.co.uk
Country
United States
ProdList
4583
Advantage
58
2A Biotech USA
Tel
--
Fax
--
Email
info@2abiotech.com
Country
United States
ProdList
1785
Advantage
58
Glentham Life Sciences Ltd
Tel
--
Fax
--
Email
info@glentham.com
Country
United States
ProdList
2026
Advantage
58
Crescent Chemical Company
Tel
--
Fax
--
Email
fran@creschem.com
Country
United States
ProdList
1441
Advantage
58
MP Biomedicals, LLC. (Division of Valiant FC Co., Ltd.)
Tel
--
Fax
--
Email
serv@mpbio.com
Country
United States
ProdList
1854
Advantage
58
CALSAK CORPORATION
Tel
--
Fax
--
Email
calsak@calsak.com
Country
United States
ProdList
430
Advantage
58
Alichem Inc.
Tel
--
Fax
--
Email
sales@alichem.com
Country
United States
ProdList
6167
Advantage
58
Redox Scientific
Tel
--
Fax
--
Email
info@redoxsci.com
Country
United States
ProdList
2380
Advantage
58
MilliporeSigma (Sigma-Aldrich Corp.)
Tel
--
Fax
--
Email
@sial.com
Country
United States
ProdList
5414
Advantage
58
Oakwood Products, Inc.
Tel
--
Fax
--
Email
sales@oakwoodchemical.com
Country
United States
ProdList
6193
Advantage
74
Accela ChemBio Inc.
Tel
--
Fax
--
Email
info@accelachem.com
Country
United States
ProdList
1054
Advantage
50
Spectrum Chemical Mfg. Corp.
Tel
--
Fax
--
Email
marketing@spectrumchemical.com
Country
United States
ProdList
3113
Advantage
60
Combi-Blocks, Inc.
Tel
--
Fax
--
Email
les@combi-blocks.com
Country
United States
ProdList
2555
Advantage
58
VWR International, LLC.
Tel
--
Fax
--
Email
@sargentwelch.com
Country
United States
ProdList
6262
Advantage
58
OX CHEM
Tel
--
Fax
--
Email
sales@ox-chem.com
Country
United States
ProdList
759
Advantage
50
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
TCI America
Tel
--
Fax
--
Email
sales@tciamerica.com
Country
United States
ProdList
6909
Advantage
75
Frontier Scientific, Inc.
Tel
--
Fax
--
Email
sales@frontiersci.com
Country
United States
ProdList
6222
Advantage
86
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
AccuStandard Inc
Tel
--
Fax
--
Email
info@bester.nl
Country
United States
ProdList
5300
Advantage
76
AlliChem, LLC
Tel
--
Fax
--
Email
sales@allichemllc.com
Country
United States
ProdList
6516
Advantage
60
ChemService Inc.
Tel
--
Fax
--
Country
United States
ProdList
6379
Advantage
68
Pfaltz & Bauer, Inc.
Tel
--
Fax
--
Email
sales@pfaltzandbauer.com
Country
United States
ProdList
6828
Advantage
72
AK Scientific, Inc.
Tel
--
Fax
--
Email
sales@aksci.com
Country
United States
ProdList
6347
Advantage
65
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
Nanjing Stellar Anatomical Model Co.,Ltd.
Tel
--
Fax
--
Email
info@anatomy-china.com
Country
United States
ProdList
83
Advantage
51
ChemSampCo, Inc.
Tel
--
Fax
--
Email
sales@chemsampco.com
Country
United States
ProdList
3585
Advantage
60
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
HONEST JOY HOLDINGS LIMITED
Tel
--
Fax
--
Email
sales@honestjoy.cn
Country
United States
ProdList
6675
Advantage
54
APAC Pharmaceutical, LLC
Tel
--
Fax
--
Email
sales@apacpharma.com
Country
United States
ProdList
6322
Advantage
38
Aceto Corporation
Tel
--
Fax
--
Email
contact@aceto.com
Country
United States
ProdList
2619
Advantage
75
ACP Chemicals Inc.
Tel
--
Fax
--
Email
service@ACPchem.com
Country
United States
ProdList
41
Advantage
42
Advanced Synthesis Technologies
Tel
--
Fax
--
Email
sales@advancedsynthesis.com
Country
United States
ProdList
4775
Advantage
61
Rintech, Inc.
Tel
--
Fax
--
Email
info@rintechinc.com
Country
United States
ProdList
3416
Advantage
60
Wilshire Chemical Company Inc.
Tel
--
Fax
--
Email
WilshrChem@AOL.COM
Country
United States
ProdList
3498
Advantage
58
Esprit Chemical Company
Tel
--
Fax
--
Email
admin@esprixtech.com
Country
United States
ProdList
1616
Advantage
55
Acros Organics USA
Tel
--
Fax
--
Email
eveleth@fisherchem.com
Country
United States
ProdList
3846
Advantage
81
American Custom Chemicals Corporation
Tel
--
Fax
--
Email
sales@acccorporation.com
Country
United States
ProdList
6820
Advantage
51
Sciencelab.com, Inc.
Tel
--
Fax
--
Email
accounting@sciencelab.com
Country
United States
ProdList
4159
Advantage
82
Advance Scientific & Chemical
Tel
--
Fax
--
Email
sales@advance-scientific.com
Country
United States
ProdList
6419
Advantage
71
Eastern Chemical Corp.
Tel
--
Fax
--
Email
eastern@u-g.com
Country
United States
ProdList
2786
Advantage
34
City Chemicals Corporation
Tel
--
Fax
--
Country
United States
ProdList
6460
Advantage
72
Beta Pharma, Inc.
Tel
--
Fax
--
Email
sales@betapharma.com
Country
United States
ProdList
6226
Advantage
60
Spectrum Chemicals & Laboratory Products
Tel
--
Fax
--
Email
sales@spectrumchemical.com
Country
United States
ProdList
6699
Advantage
77
MP Biomedicals, Inc.
Tel
--
Fax
--
Country
United States
ProdList
6561
Advantage
81
Alfa Aesar
Tel
--
Fax
--
Email
tech@alfa.com
Country
United States
ProdList
6814
Advantage
81
More
Less

View Lastest Price from 2,3-Dihydroxynaphthalene manufacturers

HebeiShuoshengImportandExportco.,Ltd
Product
2,3-Dihydroxynaphthalene 92-44-4
Price
US $6.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
2000KG/Month
Release date
2024-08-06
Hebei Longbang Technology Co., Ltd
Product
2,3-Dihydroxynaphthalene 92-44-4
Price
US $6.00/kg
Min. Order
1kg
Purity
More than 99%
Supply Ability
2000KG/Month
Release date
2024-05-24
Hebei Jingbo New Material Technology Co., Ltd
Product
2,3-Dihydroxynaphthalene 92-44-4
Price
US $8.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
200000
Release date
2024-01-02

92-44-4, 2,3-DihydroxynaphthaleneRelated Search:


  • 2,3-Dihydroxynapthalene
  • Naphthalene-2,3-diol
  • Naphthalenediol-(2,3)
  • 2,3-DIHYDROXYNAPHTHALENE
  • 2,3-NAPHTHALENEDIOL
  • 2,3-Dihydroxynaphthylene
  • 2,3-dihydrroxynaphthalene
  • 2,3-Dihydroxynaphthalene 1g [92-44-4]
  • 2,3-Dihydroxynaphthalene, 98% 50GR
  • 2,3-DIHYDROXYNAPHTHALENE, SUBL.
  • 2 3-DIHYDROXYNAPHTHALENE 98%
  • 2,3-DihydroxylNaphthalene
  • Dihydroxynaphthalene
  • 2,3-Dihydroxynaphthalene,98%
  • 2,3-Dihydroxy
  • 2,3-NAPHTHALENEDIOL FOR SYNTHESIS
  • 2,3- twohydroxy naphthalene
  • 2,3-Dihydroxynaphthalene, 99%+
  • 2,3-Dihydroxynaphthalene >=98.0% (HPLC), purified by sublimation
  • 3-Dihydroxynaphthalene
  • 2,3-Dihydroxynaphthalene &gt
  • 2,3-Naphthalenediol@100 μg/mL in AcCN
  • 2,3-Dihydroxynaphthalene ISO 9001:2015 REACH
  • 2,3-Dihydroxynaphthalene, ≥98.0% (HPLC)
  • Naphthalin-2,3-diol
  • 2,3-Dihydroxynaphthalene, ≥ 97.0%
  • 92-44-4
  • 90-44-4
  • Organic Building Blocks
  • Oxygen Compounds
  • Polyols
  • Building Blocks
  • Cell Biology
  • Chemical Synthesis
  • DIG-DY
  • Organic Building Blocks
  • Oxygen Compounds
  • Polyols
  • Bioactive Small Molecules
  • Building Blocks
  • Aromatics
  • Naphthalene derivatives