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NAPROXEN IMP M

2-Methoxynaphthalene

CAS: 93-04-9

Molecular Formula: C10H7OCH3

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NAPROXEN IMP M - Names and Identifiers

Name 2-Methoxynaphthalene
Synonyms NAPROXEN IMP M
NEROLIN YARA YARA
NEROLINE YARA YARA
2-METHOXYNAPHTHALENE
2-Methoxynaphthalene
2-NAPHTHYL METHYL ETHER
methyl β-naphthyl ether
2-Methoxynaphthaleneodium salt hydrate
Naproxen Impurity 13(Naproxen EP Impurity M)
CAS 93-04-9
EINECS 202-213-6
InChI InChI:1S/C11H10O/c1-12-11-7-6-9-4-2-3-5-10(9)8-11/h2-8H,1H3

NAPROXEN IMP M - Physico-chemical Properties

Molecular FormulaC10H7OCH3
Molar Mass158.2
Density1.064 g/mL at 25 °C (lit.)
Melting Point73-75℃
Boling Point316°C at 760 mmHg
Flash Point136.5°C
Water SolubilityINSOLUBLE
Vapor Presure0.000228mmHg at 25°C
AppearanceCrystallization
Storage ConditionRoom Temprature
Refractive Index1.5440 (estimate)
MDLMFCD00004061
Physical and Chemical Properties

character: white scaly crystal with orange flower fragrance.
melting point 73~74 ℃
boiling point 274 ℃

UseMainly used for the deployment of soap flavor, popular toilet water and Gulong perfume

NAPROXEN IMP M - Risk and Safety

Safety DescriptionS24/25 - Avoid contact with skin and eyes.
UN IDsUN 3077 9 / PGIII
WGK Germany2
RTECSQJ9468750
TSCAYes
HS Code29093090
ToxicityLD50 oral in rat: > 5gm/kg

NAPROXEN IMP M - Upstream Downstream Industry

Raw MaterialsMethanol
Sulfuric acid
1-Naphthylamine
Aurantiol (methyl anthranilate and hydroxycitronellal schiff base)
2-Methoxy-1-phenylnaphthalene
1-Iodo-2-methoxynaphthalene
2-CYANO-6-METHOXYNAPHTHALENE
2-methoxy-3-(methylthio)-naphthalen
(2-METHOXY-1-NAPHTHYL)BORONIC ACID
1-BROMO-2-METHOXYNAPHTHALENE
2-Bromo-6-methoxynaphthalene
Dimethyl acetylenedicarboxylate
4,4'-METHYLENEBIS(2,6-DIMETHYLPHENOL)
Downstream Products2-Acetyl-6-methoxynaphthalene
DL-6-METHOXY-ALPHA-METHYL-2-NAPHTHALENEMETHANOL
6-METHOXY-2-NAPHTHOIC ACID
6-Methoxy-2-naphthaldehyde
6-METHOXY-1,2,3,4-TETRAHYDRONAPHTHALENE
2-METHOXY-1-NAPHTHOIC ACID
2-Bromo-3-methoxynaphthalene
3-METHOXY-2-NAPHTHOIC ACID

NAPROXEN IMP M - Nature

Open Data Verified Data

White Crystal, melting point 73~74 ℃, boiling point 274 ℃, 138 ℃(1. 33kPa). Slightly soluble in water, methanol, ethanol, soluble in ether and carbon disulfide, soluble in benzene and chloroform. Sublimation and water vapor distillation.

Last Update:2025-06-10 22:55:16

NAPROXEN IMP M - Introduction

Slightly soluble in water, methanol, ethanol, soluble in ether and carbon disulfide, easily soluble in benzene and chloroform. Can sublimate and carry out steam distillation.
Last Update:2022-10-16 17:30:13

NAPROXEN IMP M - Safety

Open Data Verified Data

The outer woven bag, the inner plastic bag, 25kg per barrel.

Last Update:2022-01-01 10:40:03

NAPROXEN IMP M - Nature

Open Data Unverified Data
FEMA 4704 | BETA-NAPHTHYL METHYL ETHER
refractive index 1.5440 (estimate)
flash point 272-274°C
storage conditions Sealed in dry,Room Temperature
solubility H2O: soluble (completely)
morphology Crystalline Solid
color White to yellow-brown
water solubility INSOLUBLE
JECFA Number 1257
Merck 14,5997
BRN 1859408
stability Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKey LUZDYPLAQQGJEA-UHFFFAOYSA-N
NIST chemical information Naphthalene, 2-methoxy-(93-04-9)
EPA chemical information Naphthalene, 2-methoxy- (93-04-9)
Last Update:2024-04-11 22:18:20

NAPROXEN IMP M - Uses and synthesis methods

Open Data Unverified Data

β- Naphthyl methyl ether is an organic compound, also known as 2-naphthyl methyl ether. The following is about β- Introduction to the uses and synthesis methods of naphthalene methyl ether:

Usage:
Chemical intermediates: β- Naphthyl methyl ether is often used as an intermediate in organic synthesis. It can be used to synthesize various naphthyl compounds, such as naphthyl ethers, naphthyl ketones, etc., through further substitution reactions with other compounds.

Synthesis method:
β- The synthesis of naphthalene methyl ether can be carried out through the following steps:
Preparation of benzyl benzoate: Benzoic acid is reacted with alcohol to obtain benzyl benzoate.
Obtaining 2-naphthyl methanol: 2-naphthyl formate benzyl ester is subjected to thermal cracking or alkaline catalytic stripping to obtain 2-naphthyl methanol.
Methanol acidification: reacting 2-naphthalene methanol with formic acid to obtain β- Naphthyl methyl ether.
In addition, in practical applications, sometimes synthesis can also be carried out through chemical reactions starting from other compounds.

Last Update:2024-04-11 22:25:43
NAPROXEN IMP M
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Email: Int06@meryer.com
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Product Name: 2-Methoxynaphthalene Request for quotation
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Tel: 0513-66814854
Email: pules.cn@gmail.com
Mobile: +86-17551318830
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Tel: 400-968-2212
Email: 3623107365@qq.com
Mobile: 18916960931
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Product Name: 2-Methoxynaphthalene Visit Supplier Webpage Request for quotation
CAS: 93-04-9
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
QQ: 2881950922 Click to send a QQ message
Wechat: 18621343501
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Spot supply
Product Name: 2-Methoxynaphthalene Visit Supplier Webpage Request for quotation
CAS: 93-04-9
Tel: +86-531-82316028
Email: sales@zsscm.com.cn
Mobile: +8615726167122
MedChemExpress (MCE)
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CAS: 93-04-9
Tel: 609-228-6898
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View History
NAPROXEN IMP M
FLUOROZIRCONIC ACID
Mouse
Co-Formula CFS-598
OCTADECYLDIMETHYL (DIMETHYLAMINO) SILANE
RARECHEM AL BD 0183
Beta-Cyclodextrin Methyl Ethers
BLACK ACID 1
Raw Materials for NAPROXEN IMP M
Sulfuric acid
1-Iodo-2-methoxynaphthalene
2-CYANO-6-METHOXYNAPHTHALENE
Downstream Products for NAPROXEN IMP M
DL-6-METHOXY-ALPHA-METHYL-2-NAPHTHALENEMETHANOL
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