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154571

Sigma-Aldrich

1-Methoxynaphthalene

≥98%

Synonym(s):

Methyl 1-naphthyl ether, NSC 5530

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About This Item

Linear Formula:
C10H7OCH3
CAS Number:
2216-69-5
Molecular Weight:
158.20
Beilstein:
774884
EC Number:
218-696-1
MDL number:
MFCD00003924
UNSPSC Code:
12352100
PubChem Substance ID:
24849454
NACRES:
NA.22

Assay

≥98%

form

liquid

refractive index

n20/D 1.621 (lit.)

bp

135-137 °C/12 mmHg (lit.)

density

1.09 g/mL at 25 °C (lit.)

SMILES string

COc1cccc2ccccc12

InChI

1S/C11H10O/c1-12-11-8-4-6-9-5-2-3-7-10(9)11/h2-8H,1H3

InChI key

NQMUGNMMFTYOHK-UHFFFAOYSA-N

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Application

1-Methoxynaphthalene was used to study the peroxygenase activity of CcP. It was also used to synthesize prenyl naphthalen-ols.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

233.6 °F - closed cup

Flash Point(C)

112 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

154571-BULK:
154571-50G:
154571-250G:
154571-10G:
154571-VAR:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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James E Erman et al.
BMC biochemistry, 14, 19-19 (2013-07-31)
The cytochrome P450s are monooxygenases that insert oxygen functionalities into a wide variety of organic substrates with high selectivity. There is interest in developing efficient catalysts based on the "peroxide shunt" pathway in the cytochrome P450s, which uses H2O2 in
Kazutoshi Shindo et al.
Bioscience, biotechnology, and biochemistry, 75(3), 505-510 (2011-03-11)
We performed combinational bioconversion of substituted naphthalenes with PhnA1A2A3A4 (an aromatic dihydroxylating dioxygenase from marine bacterium Cycloclasticus sp. strain A5) and prenyltransferase NphB (geranyltransferase from Streptomyces sp. strain CL190) or SCO7190 (dimethylallyltransferase from Streptomyces coelicolor A3(2)) to produce prenyl naphthalen-ols.

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