What is the 2-Naphthalenol?

2-Naphthalenol is broken white shiny flakes or white powder, while it's Molecular Formula is C10H8O. broken white shiny flakes or white powder Used in Fragrance Industry: 2-Naphthalenol is used as a fragrance ingredient for its distinctive sweet, floral scent, contributing to the production of perfumes, soaps, and other cosmetic products. Its ability to impart a pleasant aroma makes it a valuable component in the creation of various scented products. Used in Chemical Synthesis: 2-Naphthalenol serves as a chemical intermediate in the synthesis of other compounds, including insecticides and pharmaceuticals. Its role in the production of these compounds highlights its importance in the chemical industry and its contribution to the development of various consumer and industrial products. Safety Considerations: While 2-Naphthalenol is not considered to be highly toxic, it can cause irritation to the skin, eyes, and respiratory system upon exposure. Therefore, it is crucial to handle and store this chemical with care to prevent any potential health and safety risks, ensuring the well-being of individuals involved in its production, use, and disposal.

What is the CAS number for 2-Naphthalenol?

The CAS number of 2-Naphthalenol is 135-19-3.

What is 2-Naphthalenol (135-19-3) used for?

2-Naphthalenol, also known as β-naphthol, is a white crystalline compound characterized by a strong, sweet, floral odor. It is derived from naphthalene and is recognized for its versatile applications in various industries due to its unique chemical properties.InChI:InChI=1/C10H8O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H

What is the 2-Naphthalenol?

2-Naphthalenol is broken white shiny flakes or white powder, while it's Molecular Formula is C10H8O. broken white shiny flakes or white powder Used in Fragrance Industry: 2-Naphthalenol is used as a fragrance ingredient for its distinctive sweet, floral scent, contributing to the production of perfumes, soaps, and other cosmetic products. Its ability to impart a pleasant aroma makes it a valuable component in the creation of various scented products. Used in Chemical Synthesis: 2-Naphthalenol serves as a chemical intermediate in the synthesis of other compounds, including insecticides and pharmaceuticals. Its role in the production of these compounds highlights its importance in the chemical industry and its contribution to the development of various consumer and industrial products. Safety Considerations: While 2-Naphthalenol is not considered to be highly toxic, it can cause irritation to the skin, eyes, and respiratory system upon exposure. Therefore, it is crucial to handle and store this chemical with care to prevent any potential health and safety risks, ensuring the well-being of individuals involved in its production, use, and disposal.

What is the CAS number for 2-Naphthalenol?

The CAS number of 2-Naphthalenol is 135-19-3.

What is 2-Naphthalenol (135-19-3) used for?

2-Naphthalenol, also known as β-naphthol, is a white crystalline compound characterized by a strong, sweet, floral odor. It is derived from naphthalene and is recognized for its versatile applications in various industries due to its unique chemical properties.InChI:InChI=1/C10H8O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H

Product classification

Featured Products

2-Naphthol

Chemical raw materials, non-pharmaceuticals.
Product Name: 2-Naphthol
CasNo: 135-19-3
Purity:
Appearance: broken white shiny flakes or white powder

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Email:wibson.aris@gmail.com

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CasNo： 135-19-3

Molecular Formula： C₁₀H₈O

Appearance： broken white shiny flakes or white powder

Manufacturer Supply Best Quality 2-Naphthol 135-19-3 with Efficient Transportation

Molecular Formula:C10H8O
Molecular Weight:144.173
Appearance/Colour:broken white shiny flakes or white powder
Vapor Pressure:0.00162mmHg at 25°C
Melting Point:120-122 °C(lit.)
Refractive Index:1.677
Boiling Point:285.499 °C at 760 mmHg
Flash Point:144.002 °C
PSA：20.23000
Density:1.182 g/cm³
LogP:2.54540

2-Naphthalenol(Cas 135-19-3) Usage

General Description

Asiaticoside is a triterpenoid compound derived from Centella asiatica, known for its potent skin-repairing and anti-inflammatory properties. It promotes collagen production, aiding in wound healing and restoring skin elasticity. This compound also offers strong antioxidant benefits, reducing free radical damage and UV-induced pigmentation. Widely used in cosmetics and pharmaceuticals, Asiaticoside is a key component in treating skin disorders such as psoriasis and ulcers, and it also enhances the skin’s protective barrier. Additionally, it has neuroprotective and anti-inflammatory effects, making it a valuable component in both traditional medicine and modern therapeutic applications.

Manufacturer

Shanghai Wibson Biotechnology Co., Ltd. is a high-tech enterprise that mainly develops and sells pharmaceutical and chemical raw materials and other related products. The company has advanced and perfect supporting system and has formed advanced chemical synthesis technology, which can quickly meet the personalized needs and series development from suitable testing to industrial production. Products are exported to Russia, Southeast Asia and other countries, in the world has a very high reputation and visibility. The company has strong financial strength and a good operating environment, can provide customers with high-quality, efficient and fast services. We have 16 years of experience in R&D and manufacturing, we have rich experience in shipping, many well-known companies have cooperated with us, and are good at shipping various chemical products with us.We can provide OEM,ODM service with low MOQ!

InChI:InChI=1/C10H8O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H

135-19-3 Relevant articles

Adsorption characteristics of 1,2,4-trichlorobenzene, 2,4,6-trichlorophenol, 2-naphthol and naphthalene on graphene and graphene oxide

Zhiguo Pei a , Lingyun Li b , Lixiang Sun c , Shuzhen Zhang a , Xiao-quan Shan a , Shuang Yang a , Bei Wen a

, Carbon Volume 51 , January 2013, Pages 156-163

Theoretical calculation ascribed this to higher π-electron density of anionic 2-naphthol than that of neutral 2-naphthol, which facilitated the π–π interaction formation with G. For GO, the adsorption affinity of four aromatics increased in the order: NAPH < TCB < TCP < 2-naphthol. FTIR results revealed that TCB, TCP and 2-naphthol were adsorbed on G mainly via π–π interaction. In contrast, high adsorption of TCP and 2-naphthol on GO was attributed to the formation of H-bonding between hydroxyl groups of TCP and 2-naphthol and O-containing functional groups on GO.

Anodic oxidation of 2-naphthol at boron-doped diamond electrodes

M. Panizza a , P.A. Michaud b , G. Cerisola a , Ch. Comninellis b

, Journal of Electroanalytical Chemistry Volume 507, Issues 1–2 , 13 July 2001, Pages 206-214

In this work the anodic oxidation of 2-naphthol has been investigated on synthetic BDD film electrodes in sulfuric acid medium. Cyclic voltammetry and bulk electrolysis were carried out to explore the activity of BDD for 2-naphthol oxidation under different experimental conditions.

PHOTOCHEMICAL REACTIONS OF NAPHTHYL-VINYL NON-CONJUGATED BICHROMOPHORIC SYSTEMS

Kashoulis, Annoula,Gilbert, Andrew,Ellis-Davies, Graham

, p. 2905 - 2908 (1984)

2-(1-Naphthyl)ethyl vinyl ether undergoe...

Two channels of electron transfer observed for the reaction of n-butyl chloride parent radical cations with naphthols and hydroxybiphenyls

Mohan,Hermann,Naumov,Mittal,Brede

, p. 5754 - 5762 (1998)

Pulse radiolysis of naphthols (NpOH) and...

Acid-Catalyzed Versus Thermally Induced C1-C1′ Bond Cleavage in 1,1′-Bi-2-naphthol: An Experimental and Theoretical Study

Genaev, Alexander M.,Shchegoleva, Lyudmila N.,Salnikov, George E.,Shernyukov, Andrey V.,Shundrin, Leonid A.,Shundrina, Inna K.,Zhu, Zhongwei,Koltunov, Konstantin Yu.

, p. 7238 - 7243 (2019)

Experiments show that 1,1′-bi-2-naphthol...

Effect of Confinement on the Properties of Sequestered Mixed Polar Solvents: Enzymatic Catalysis in Nonaqueous 1,4-Bis-2-ethylhexylsulfosuccinate Reverse Micelles

Durantini, Andres M.,Falcone, R. Dario,Silber, Juana J.,Correa, N. Mariano

, p. 1678 - 1685 (2016)

The influence of different glycerol, N,N...

Photocatalytic Reductive C-O Bond Cleavage of Alkyl Aryl Ethers by Using Carbazole Catalysts with Cesium Carbonate

Yabuta, Tatsushi,Hayashi, Masahiko,Matsubara, Ryosuke

, p. 2545 - 2555 (2021/02/01)

Methods to activate the relatively stabl...

135-19-3 Process route

: 4323-69-7
[1]naphthyl-nitro-amine

: 7732-18-5
water

: 91-20-3,71998-51-1,72931-45-4
naphthalene

: 134-32-7
1-amino-naphthalene

: 135-19-3
β-naphthol

Conditions

Conditions	Yield

: 13463-67-7
titanium dioxide

: 135-19-3
β-naphthol