ChemicalBook > CAS DataBase List > 2-Naphthol

2-Naphthol

Product Name
2-Naphthol
CAS No.
135-19-3
Chemical Name
2-Naphthol
Synonyms
naphthalen-2-ol;2-naphthalenol;2-HYDROXYNAPHTHALENE;BETA NAPTHOL;BETA-NAPHTHOL;2-Naphtol;β-Naphthol;B-NAPHTHOL;2-Naftol;BETA NAPHTHO
CBNumber
CB9336283
Molecular Formula
C10H8O
Formula Weight
144.17
MOL File
135-19-3.mol
More
Less

2-Naphthol Property

Melting point:
120-122 °C(lit.)
Boiling point:
285-286 °C(lit.)
Density 
1,28 g/cm3
vapor density 
4.97 (vs air)
vapor pressure 
10 mm Hg ( 145.5 °C)
refractive index 
1.5762 (estimate)
Flash point:
153 °C
storage temp. 
Store below +30°C.
solubility 
methanol: soluble1g/10 mL, clear, colorless to light yellow
pka
9.51(at 25℃)
form 
Powder, Crystals or Granules
color 
White
Odor
faint phenol-like odor
PH Range
Non& uorescence (8.5) to blue & uorescence (9.5)
Water Solubility 
1 g/L (20 ºC)
λmax
226nm, 265nm, 275nm, 286nm, 320nm, 331nm
Merck 
14,6384
BRN 
742134
Stability:
Stable. Combustible. Dust may form explosive mixture with air. Incompatible with strong oxidizing agents, phenol.
Major Application
Display device, semiconductors, photoimaging materials, inks, toner, chalk, security paper, molding materials, tin plating method, rubber, adhesive, leather, detergent, hair dyes, antimitotic drug, anticancer agent, antiinflammatory agent, treatment of acne vulgaris (pimples) and other dermal ailments (rashes, scratches, blemishes, hair loss), disorders
InChIKey
JWAZRIHNYRIHIV-UHFFFAOYSA-N
LogP
1.89 at 20℃
CAS DataBase Reference
135-19-3(CAS DataBase Reference)
NIST Chemistry Reference
2-Naphthalenol(135-19-3)
EPA Substance Registry System
2-Naphthalenol (135-19-3)
More
Less

Safety

Hazard Codes 
Xn,N
Risk Statements 
20/22-50
Safety Statements 
24/25-61
RIDADR 
UN 3077 9/PG 3
WGK Germany 
2
RTECS 
QL2975000
F 
8
Autoignition Temperature
430 °C
TSCA 
Yes
HazardClass 
9
PackingGroup 
III
HS Code 
29071590
Hazardous Substances Data
135-19-3(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: 1960 mg/kg LD50 dermal Rabbit > 10000 mg/kg
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H317May cause an allergic skin reaction

H318Causes serious eye damage

H400Very toxic to aquatic life

Precautionary statements

P273Avoid release to the environment.

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

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

P302+P352IF ON SKIN: wash with plenty of soap and water.

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

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
8.22290
Product name
2-Naphthol
Purity
for synthesis
Packaging
250g
Price
$48.2
Updated
2024/03/01
Sigma-Aldrich
Product number
8.22290
Product name
2-Naphthol
Purity
for synthesis
Packaging
1kg
Price
$76.9
Updated
2024/03/01
Sigma-Aldrich
Product number
130109
Product name
2-Naphthol
Purity
98%
Packaging
250g
Price
$53.8
Updated
2024/03/01
Sigma-Aldrich
Product number
130109
Product name
2-Naphthol
Purity
98%
Packaging
1kg
Price
$72.7
Updated
2024/03/01
Sigma-Aldrich
Product number
70450
Product name
2-Naphthol
Purity
fluorescence indicator, ≥99.0%
Packaging
500g
Price
$161
Updated
2022/05/15
More
Less

2-Naphthol Chemical Properties,Usage,Production

Chemical Properties

2-Naphthol is a white, crystalline solid. Slight phenolic odor. Darkens in air and on exposure to light. 2-Naphthol [135-19-3] b-naphthol, 2- naphthalenol, 2-hydroxynaphthalene, C10H8O, Mr 144.16, forms colorless plates upon sublimation, which darken on exposure to air or light. Unlike 1-naphthol it is nonvolatile in steam. 2-Naphthol is reduced with sodium or with hydrogen in the presence of a catalyst to give mainly 1,2,3,4-tetrahydro-2-naphthol (unlike 1- naphthol which gives the arylphenol under the same conditions). 

Physical properties

White glossy flakes or white powder. Insoluble in water, soluble in ethanol, ether, chloroform, glycerol and alkali solution.

Uses

Has been used as antiseptic, anthelmintic and counter-irritant in alopecia.

Uses

2-Naphthol is used in the manufacture of dyes, perfumes, and medicinal organics, and in the production of antioxidants for synthetic rubber.

Application

It is used to produce Tobias acid, J acid, 2-hydroxy-3-naphthoic acid and azo dyes, and it is the raw material for rubber antioxidants, mineral dressing agents, fungicides, antiseptics, preservatives, etc.
As feed preservative. In China, it can be used for citrus preservation, the maximum dosage amount is 0.1 g/kg and the residue amount should be no more than 70 mg/kg.
2-Naphthol, also called β-naphthol, 2-naphthalenol, is the intermediate for plant growth regulator, 2-naphthoxyacetic acid.
As analytic agent, absorbent of ethylene and carbon monoxide, and fluorescence indicator.
Important organic raw material and dye intermediate, used to produce Tobias acid, butyric acid, β-hydroxynaphthoic acid and used to produce N-phenyl-2-naphthylamine, Diafen NN and other antioxidant, organic pigments, and fungicides.
For the detection of bromine, chlorine, chlorate, niobium, copper, nitrite, and potassium. Substrate for fluorometric assay of phenol sulfotransferase. Acid and alkali indicator, dyes, organic synthesis, qualitative determination of allyl alcohol, methanol, chloroform, etc. Absorbent of carbon monoxide, ethanol, and fluorescence indicator. Determination of carbon monoxide, copper, nitrite, and potassium. Ethylene absorbent.

Definition

ChEBI: 2-naphthol is a naphthol carrying a hydroxy group at position 2. It has a role as an antinematodal drug, a genotoxin, a human xenobiotic metabolite, a mouse metabolite, a human urinary metabolite and a radical scavenger.

Preparation

2-Naphthol is produced by caustic fusion of naphthalene-2-sulfonic acid. Typically, the sodium salt of the sulfonic acid is added gradually to 50 % sodium hydroxide liquor at 300℃; the melt is then heated further at 320℃ in a gas-fired iron vessel with vigorous agitation. After completion of the reaction, the melt is run into excess water, possibly including filtrate from the previous batch at a proven tolerable level, and the naphtholate solution is neutralized to pH 8 with dilute sulfuric acid. If the temperature is maintained at >100℃ during neutralization, the crude product comes out of solution as an oil, which is separated, washed with hot water, and distilled under vacuum to give pure 2-naphthol. The molten material is processed through a flaker to give the final product for packaging. The fusion yield is about 80 % of the theoretical value, resulting in an overall yield of 70 % based on naphthalene. Typical specifications for 2-naphthol are clear solution in dilute caustic soda,  mp 120.5℃, and 1-naphthol content<0.3 %.

Reactions

2-Naphthol is naphthalene homologues of phenol, with the hydroxyl group being more reactive than in the phenols.2-Naphthol converts to 2-naphthalenethiol by reaction with dimethylthiocarbamoyl chloride via the Newman–Kwart rearrangement.

Synthesis Reference(s)

Journal of the American Chemical Society, 72, p. 4884, 1950 DOI: 10.1021/ja01167a009
Synthesis, p. 437, 1985 DOI: 10.1055/s-1985-31235

General Description

2-Naphthol is a hydroxyarene molecule, which when electronically excited forms strong acid. Excited 2-Naphthol dissociates only in water. It has a slight phenolic odor. It is incompatible with strong oxidizing agents, strong bases, acid chlorides and acid anhydrides. It is one of the most commonly used fluorescence dye.

Health Hazard

Although the toxicity of 2-naphthol is of low order in test animals, ingestion of large amounts may result in nausea, vomiting, diarrhea, abdominal pain, convulsions, and hemolytic anemia. Death may result from respiratory failure. The oral LD50 value in rats is in the range 2000 mg/kg. 2-Naphthol is slightly more toxic than 1-naphthol [9015-3], the oral LD50 value of which is in the range 2500 mg/kg.
Skin contact can produce peeling of the skin and pigmentation.

Fire Hazard

Noncombustible solid.

Chemical Reactivity

2-naphthol can be oxidation with ferric chloride forms 2,20 -dihydroxy-1,10 -binaphthyl, with any blue coloration indicating the presence of 1- naphthol.
Air oxidation at 300℃ with a vanadium pentoxide catalyst also yields 1,10 -bi-2-naphthol, which dehydrates at higher temperature to the oxide and finally decomposes to give benzoic acid.
2-naphthol can reacte with phosphorus pentachloride at 150℃ gives 2-chloronaphthalene or at lower temperature, tri-2-naphthyl phosphate (mp 111℃), which can be isolated after treatment of the reaction mixture with alkali.
Reaction with one equivalent of bromine in acetic acid gives 1-bromo-2-naphthol, whereas excess bromine yields 1,6-dibromo-2-naphthol. The latter is readily debrominated in dilute mineral acid to yield 6-bromo-2-naphthol. 

Safety Profile

Poison by ingestion, inhalation, and subcutaneous routes. Mutation data reported. A skin and eye irritant. Combustible when exposed to heat or flame. To fight fire, use CO2, dry chemical. Incompatible with antipyrine, camphor, phenol, ferric salts, menthol, potassium permanganate and other oxidzing materials, urethane.

Potential Exposure

A potential danger to those involved in rubber antioxidant production, synthesis of dyes; leather processing; fungicides, pharmaceuticals, and perfumes. Used as an antioxidant for fats, oils; as an antiseptic; in insecticides.

Shipping

UN2811 Toxic solids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required. UN3077 Environmentally hazardous substances, solid, n.o.s., Hazard Class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required.

Purification Methods

Crystallise 2-naphthol from aqueous 25% EtOH (charcoal), H2O, *benzene, toluene or CCl4. Alternatively, extract it repeatedly with small amounts of EtOH, followed by dissolution in a minimum volume of EtOH and precipitation with distilled water, then drying over P2O5 under vacuum. It has also been dissolved in aqueous NaOH and precipitated by adding acid (repeat several times), then precipitated from *benzene by addition of heptane. Final purification can be by zone melting or sublimation in vacuo. The 4-nitrobenzoate has m 104o (from EtOH). [Bardez et al. J Phys Chem 89 5031 1985, Kikuchi et al. J Phys Chem 91 574 1987, Beilstein 6 IV 4253.]

Properties and Applications

white crystalline, with phenol smell. Industrial goods for hoar chip or powder. Melting point 121 ~ 123 ℃, 285 ℃ ~ 286 boiling point, flash point 161 ℃. This product soluble in water, ethanol, ethyl ether, chloroform, glycerin and alkali solution, can the sublimation, with steam evaporate out; Long storage or light color in turn dark, can happen oxidation, reduction, nitrification and nitrosation reaction, and products, light and heat, halogenating role, etc.

Incompatibilities

Dust or powder may form explosive mixture with air. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides, iron salts; 2,3-dimethyl-1- phenyl-3-pyrazolin-5-one (antipyrine); camphor, phenol, menthol, urethane.

Waste Disposal

Mix with flammable solvent and atomize into an incinerator.

2-Naphthol Preparation Products And Raw materials

Raw materials

Naphthalene Congo red paper Sodium sulfite Solid caustic soda Phenolphthalein Sulfur dioxide Sodium 2-naphthalenesulfonate Sodium bisulfite solution Nitric acid Sodium hydroxide Naphthalene-2-sulfonic acid Sulfuric acid

Preparation Products

synthetic tanning agent No.9 6-HYDROXY-2-NAPHTHALENEBORONIC ACID Pigment Red 53:1 Lithol Red Acid Black 168 2-Aminonaphthalene-1-sulfonic acid 2-Amino-3,6,8-naphthalenetrisulfonic acid 2-Naphthaleneboronic acid 2-Naphthylamine Mordant Black 17 Neutral Black 2S-RL Disodium 2-naphthol-3,6-disulfonate Eriochrome Black A (R)-(+)-1,1'-Bi-2-naphthol Pigment Red 21 Pigment Red 4 3-Hydroxy-2-naphthoic acid 2-FLUORONAPHTHALENE 6-Amino-4-hydroxy-2-naphthalenesulfonic acid ACID BLUE 161, PURE Pigment Orange 5 1-Amino-2-naphthol-4-sulfonic acid Eriochrome Black T 1-Diazo-2-naphthol-4-sulfonic acid (S)-(-)-1,1'-Bi-2-naphthol 2-HYDROXY-1-NAPHTHOIC ACID Pigment Red 3 Sodium 6-hydroxynaphthalene-2-sulfonate N-(2-Naphthyl)aniline NAPROANILIDE synthetic tanning agent PNC Indigo Carmine 2-Acetyl-6-methoxynaphthalene Naproxen synthetic tanning agent HV
More
Less

2-Naphthol Suppliers

Americas 1 Australia 2 Austria 1 Belgium 3 Bulgaria 1 Canada 6 China 550 Czech Republic 5 Denmark 1 Europe 4 France 7 Germany 13 Hungary 1 India 111 Italy 1 Japan 11 Malaysia 1 Norway 1 Poland 1 Russia 1 Slovakia 1 South Korea 5 Spain 1 Switzerland 2 The Netherlands 5 Ukraine 1 United Kingdom 18 United States 79 Global 834
TCI Chemicals (India) Pvt. Ltd.
Tel
--
Fax
--
Email
sales-in@tcichemicals.com
Country
India
ProdList
6768
Advantage
58
Jigs chemical
Tel
--
Fax
--
Email
info@jigschemical.com
Country
India
ProdList
318
Advantage
58
Sisco Research Laboratories Pvt. Ltd.
Tel
--
Fax
--
Email
marketing@srlchem.com
Country
India
ProdList
4315
Advantage
58
Triveni chemicals
Tel
--
Fax
--
Email
sales@trivenichemical.com
Country
India
ProdList
6088
Advantage
58
Alfa Aesar
Tel
--
Fax
--
Email
tech@alfa.com
Country
India
ProdList
6905
Advantage
58
Dharani Export-Import Services (P) Ltd.
Tel
--
Fax
--
Email
info@dharani-exim.com
Country
India
ProdList
171
Advantage
58
Sudarshan Pharma Industries Limited.
Tel
--
Fax
--
Email
@sudarshangrp.com
Country
India
ProdList
157
Advantage
58
J. N. Chemical
Tel
--
Fax
--
Email
info@jnchemicals.com
Country
India
ProdList
139
Advantage
58
Ankita Chemicals Corp.
Tel
--
Fax
--
Email
ankitachemco@yahoo.com
Country
India
ProdList
4
Advantage
58
Sanchi Organics Pvt. Ltd. (Oswal Udhyog Group)
Tel
--
Fax
--
Email
hitesh@oswaludhyog.com
Country
India
ProdList
3
Advantage
58
H. Ramesh Kumar
Tel
--
Fax
--
Country
India
ProdList
117
Advantage
58
ABC Chemical Exports Private Limited
Tel
--
Fax
--
Country
India
ProdList
5
Advantage
58
Shivam Pharma Chemicals
Tel
--
Fax
--
Email
info@shivampharma.com
Country
India
ProdList
656
Advantage
58
Laxmi Dye-Chem.
Tel
--
Fax
--
Email
info@laxmidyechem.com
Country
India
ProdList
30
Advantage
58
Arihant Chemical Corporation
Tel
--
Fax
--
Email
arihant7@vsnl.com
Country
India
ProdList
48
Advantage
58
Aashta Ipmex
Tel
--
Fax
--
Email
aasthaimpex@gmail.com
Country
India
ProdList
24
Advantage
58
Suraj Impex
Tel
--
Fax
--
Email
surajimpexindia@gmail.com
Country
India
ProdList
9
Advantage
58
Associated Agencies
Tel
--
Fax
--
Email
info@assoagen.com
Country
India
ProdList
29
Advantage
58
Indian Commercial Company Pvt. Ltd. (ICC)
Tel
--
Fax
--
Email
sales@iccindia.com
Country
India
ProdList
38
Advantage
58
Hindchem Corporation
Tel
--
Fax
--
Country
India
ProdList
118
Advantage
58
Jigchem Universal
Tel
--
Fax
--
Country
India
ProdList
76
Advantage
58
Colour Finders
Tel
--
Fax
--
Email
email@colourfinders.com
Country
India
ProdList
73
Advantage
58
Sachin Chemicals
Tel
--
Fax
--
Email
sachinchemicals@gmail.com
Country
India
ProdList
140
Advantage
58
Suvchem
Tel
--
Fax
--
Email
sales@suvchem.com
Country
India
ProdList
180
Advantage
58
Pharma Affiliates
Tel
--
Fax
--
Email
@pharmaffiliates.com
Country
India
ProdList
6754
Advantage
58
Harshlaxmi Chemisolv
Tel
--
Fax
--
Email
info@harshlaxmi.com
Country
India
ProdList
9
Advantage
58
Shri Raj Industries
Tel
--
Fax
--
Email
info@shrirajind.com
Country
India
ProdList
47
Advantage
58
Manali Chemicals
Tel
--
Fax
--
Country
India
ProdList
79
Advantage
58
Labort Fine Chem Pvt,. Ltd.
Tel
--
Fax
--
Email
info@laboratorychemical.net
Country
India
ProdList
34
Advantage
58
Macson Products
Tel
--
Fax
--
Country
India
ProdList
13
Advantage
58
Clearsynth Labs
Tel
--
Fax
--
Email
fo@clearsynth.com
Country
India
ProdList
3887
Advantage
58
Oceanic Pharmachem Pvt., Ltd. (OPPL)
Tel
--
Fax
--
Email
info@oceanicpharmachem.com
Country
India
ProdList
946
Advantage
58
Chemrich Fine Chemicals Pvt., Ltd.
Tel
--
Fax
--
Email
info@chemrichfine.com
Country
India
ProdList
399
Advantage
58
Advent Chembio Pvt., Ltd.
Tel
--
Fax
--
Email
sales@adventchembio.com
Country
India
ProdList
623
Advantage
58
Satyan Pharmaceuticals Pvt Ltd.
Tel
--
Fax
--
Email
common@satyanltd.com
Country
India
ProdList
54
Advantage
58
Sandeep Organics Pvt. Ltd.
Tel
--
Fax
--
Email
sanchem@sandeeporganics.com
Country
India
ProdList
21
Advantage
58
Manav Bio -Chem Impex Pvt Ltd
Tel
--
Fax
--
Email
cheminquiry@gmail.com
Country
India
ProdList
204
Advantage
58
ADCI Dye-Chem Private Limited
Tel
--
Fax
--
Country
India
ProdList
7
Advantage
58
Azole Rasayanas India Private Limited
Tel
--
Fax
--
Email
info@azolerasayanas.com
Country
India
ProdList
681
Advantage
58
Techno Pharmchem
Tel
--
Fax
--
Email
tecpharm@gmail.com
Country
India
ProdList
173
Advantage
58
Astron Chemical
Tel
--
Fax
--
Email
ast_ron@hotmail.com
Country
India
ProdList
78
Advantage
58
Ganpati Exim Pvt Ltd
Tel
--
Fax
--
Email
info@ganpatiexim.com
Country
India
ProdList
24
Advantage
58
Bhimani Group
Tel
--
Fax
--
Email
rupesh@bhimanigroup.com
Country
India
ProdList
29
Advantage
58
Rasayano
Tel
--
Fax
--
Email
rasayano@gmail.com
Country
India
ProdList
6
Advantage
58
Black Rose Industries Ltd.
Tel
--
Fax
--
Email
info@blackrosechemicals.com
Country
India
ProdList
45
Advantage
58
Cosmos Intenational
Tel
--
Fax
--
Email
jatin.nk@gmail.com
Country
India
ProdList
125
Advantage
58
Asiatic Colour-Chem Ind. Ltd.
Tel
--
Fax
--
Email
mahesh@asiaticcolour.com
Country
India
ProdList
18
Advantage
58
Meru Chem Pvt. Ltd.
Tel
--
Fax
--
Email
meruchempltd@gmail.com
Country
India
ProdList
174
Advantage
58
Sanjay Chemicals (India) Pvt., Ltd.
Tel
--
Fax
--
Email
abdul@sanjaychemindia.com
Country
India
ProdList
159
Advantage
58
Sai Quest Syn. Ltd
Tel
--
Fax
--
Country
India
ProdList
268
Advantage
58
More
Less

View Lastest Price from 2-Naphthol manufacturers

Jinan Finer Chemical Co., Ltd
Product
2-Naphthol 135-19-3
Price
US $2.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
1000mt/year
Release date
2022-12-29
Hebei Zhuanglai Chemical Trading Co.,Ltd
Product
2-Naphthol 135-19-3
Price
US $99.00-35.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20ton
Release date
2024-05-16
Hebei Zhuanglai Chemical Trading Co Ltd
Product
Beta Naphthol 135-19-3
Price
US $150.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
500kg
Release date
2024-12-12

135-19-3, 2-NaphtholRelated Search:

Terbinafine hydrochloride Sodium hydroxide Terbinafine Hydrochloride Hydroxy silicone oil 2-(Phenylmethoxy)-naphthalene Ammonium hydroxide Ethyl acetate Methylparaben Lithium hydroxide monohydrate Triclosan 4-Hydroxybenzoic acid 4-Hydroxybenzaldehyde 2,3,4-Trihydroxybenzoic acid Phenmedipham 1-(1-NAPHTHYL)-2-THIOUREA Aluminum hydroxide Glycolic acid 1-(2-Pyridylazo)-2-naphthol

  • c.i.37500
  • c.i.azoiccouplingcomponent1
  • c.i.developer5
  • Developer A
  • Developer AMS
  • Developer BN
  • developera
  • developerams
  • developerbn
  • naphthyl hydroxide
  • Naphthyl alcohol
  • NAPHTHOL, B-
  • iso-Napthol
  • BETA NAPHTHO
  • 2-naphthol (beta)
  • Beta Naphthol (2-Naphthol)
  • B-NAPHTOL
  • BETA NAPHTHOL 99% MIN
  • 2-NAPHTHOL (BETA), FOR ANALYTICAL PURPOS ES
  • 2-NAPHTHOL R. G., REAG. PH. EUR.
  • 2-NAPHTHOL POWDER
  • 2-NAPHTHOL (BETA), FLUORESCENCE INDICATO R
  • betaNaphthol, Low Naphthalene
  • 2-NaphtholA.R.
  • 2-NaphtholGr
  • 2-NaphtholForSynthesis
  • BetaNaphthol99%
  • 2-Naphthol, 97+%
  • β-Monoxynaphthalene
  • 2-Naphthol, 99+%
  • 2-Naphthol, tech., 97%
  • 2-NAPHTHOL,PURIFIED
  • 2-NAPHTHOL,REAGENT
  • 2-HYDROXYNAPTHALENE
  • NAPHTHOL-2
  • BETA NAPHTHOL ( 2-HYDROXY NAPHTHALENE)
  • 2-NAPHTHOL, 98+%
  • 2-NAPHTHOL(β-NAPHTHOL)
  • B-NAPHTHOL WITH GC
  • Naphth-2-ol
  • b-NAPHTHOL extrapure AR
  • 2-Naphthol 98%
  • 2-Naftol
  • 2-Naftolo
  • 2-Naphtol
  • Antioxygene BN
  • Azogen Developer A
  • azogendevelopera
  • azoiccouplingcomponent1
  • beta-Monoxynaphthalene
  • beta-Naftol
  • beta-Naftolo
  • beta-Naphthyl alcohol
  • beta-Naphthyl hydroxide
  • 2-Hydroxynaphthalene N-Hydroxy-N-nitrosobenzenamine ammonium salt
  • beta-naphthylalcohol
  • beta-naphthylhydroxide
  • beta-Naphtol