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W509000

Sigma-Aldrich

2-Methoxynaphthalene

≥99%

Sinonimo/i:

Methyl 2-naphthyl ether

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About This Item

Formula condensata:
C10H7OCH3
Numero CAS:
93-04-9
Peso molecolare:
158.20
Beilstein:
1859408
Numero CE:
202-213-6
Numero MDL:
MFCD00004061
Codice UNSPSC:
12164502
ID PubChem:
329830745
Numero Flavis:
4.074

Origine biologica

synthetic

Grado

Kosher

Saggio

≥99%

P. ebollizione

274 °C (lit.)

Punto di fusione

70-73 °C (lit.)

Densità

1.064 g/mL at 25 °C (lit.)

applicazioni

flavors and fragrances

Stringa SMILE

COc1ccc2ccccc2c1

InChI

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

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Caratteristiche e vantaggi

Intensely sweet, floral, mild orange blossom

Altre note

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Pittogrammi

Exclamation markEnvironment
GHS07,GHS09

Avvertenze

Warning

Indicazioni di pericolo

H319,H411

Classi di pericolo

Aquatic Chronic 2 - Eye Irrit. 2

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
10129KD
S29089
11211AG
09210AN
13917TQ

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P Di Gennaro et al.
Biotechnology and bioengineering, 93(3), 511-518 (2005-09-30)
The bioconversion of naphthalene to the 1,2-dihydro-1,2-dihydroxy derivative was performed in good yield using an Escherichia coli recombinant strain carrying Pseudomonas fluorescens N3 dioxygenase. However, the efficiency of such transformation is affected by many process parameters, and their optimization is
G M Whited et al.
Bioorganic & medicinal chemistry, 2(7), 727-734 (1994-07-01)
2-Methoxynaphthalene was subjected to biooxidation by whole cells of six organisms: Pseudomonas putida F39/D containing toluene dioxygenase, Escherichia coli JM109(pDTG601), containing recombinant toluene dioxygenase from Pp F39/D, Pseudomonas sp. NCIB 9816/11, containing naphthalene dioxygenase. E. coli JM109(pDTG141), containing recombinant naphthalene
H Widén et al.
Food additives and contaminants, 22(7), 681-692 (2005-07-16)
Mineral water and soft drinks with a perceptible off-odour were analysed to identify contaminants originating from previous misuse of the refillable polyethylene terephthalate (PET) bottle. Consumers detected the off-odour after opening the bottle and duly returned it with the remaining
Mingzhang Gao et al.
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 68(3), 459-465 (2010-01-12)
Carbon-11-labeled piperidine ring of N-[omega-(6-methoxynaphthalen-1-yl)alkyl] derivatives were first designed and synthesized as new selective PET sigma(1) receptor probes. The target tracers were prepared by O-[(11)C]methylation of their corresponding phenolic hydroxyl precursors using [(11)C]CH(3)OTf under basic conditions and isolated by a
R R Price et al.
Journal of microencapsulation, 10(2), 215-222 (1993-04-01)
Many natural products that exhibit biocidal activity have poor solubility in water. In order to explore the prolonged delivery of these compounds from microtubules we have utilized 2-methoxynaphthalene as a model to elucidate release characteristics of hydrophobic compounds entrapped in
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