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Documenti fondamentali

W319309

Sigma-Aldrich

1-Methylnaphthalene

≥95%

Sinonimo/i:

α-methylnaphthalene

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About This Item

Formula condensata:
C10H7CH3
Numero CAS:
Peso molecolare:
142.20
Numero FEMA:
3193
Beilstein:
506793
Numero CE:
N° CoE:
11009
Numero MDL:
Codice UNSPSC:
12164502
ID PubChem:
Numero Flavis:
1.014
NACRES:
NA.21
Organolettico:
earthy
Grado:
Fragrance grade
Halal
Kosher
Origine biologica:
synthetic
agenzia:
follows IFRA guidelines
Allergene alimentare:
no known allergens

Origine biologica

synthetic

Livello qualitativo

Grado

Fragrance grade
Halal
Kosher

agenzia

follows IFRA guidelines

Conformità normativa

EU Regulation 1223/2009

Saggio

≥95%

Stato

liquid

Temp. autoaccensione

984 °F

Indice di rifrazione

n20/D 1.615 (lit.)

P. ebollizione

240-243 °C (lit.)

Punto di fusione

−22 °C (lit.)

Densità

1.001 g/mL at 25 °C (lit.)

applicazioni

flavors and fragrances

Documentazione

see Safety & Documentation for available documents

Allergene alimentare

no known allergens

Allergene in fragranze

no known allergens

Organolettico

earthy

Stringa SMILE

Cc1cccc2ccccc12

InChI

1S/C11H10/c1-9-5-4-7-10-6-2-3-8-11(9)10/h2-8H,1H3
QPUYECUOLPXSFR-UHFFFAOYSA-N

Informazioni sul gene

human ... CYP1A2(1544)

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Descrizione generale

1-Methylnaphthalene occurs in Chinese raw spirits, brown millet, milled millet and millet bran. This volatile organic compound (VOC) is also found in the diesel engine exhaust gas and in the manures of cow, hog and chicken.

Applicazioni


  • Viscosities and Densities of Binary and Ternary Mixtures of Aliphatic and Polyaromatic Hydrocarbons: Pyrene +1-Methylnaphthalene + Dodecane at T = (293.15 to 343.15) K. Experiment and Modeling.: This research presents experimental data and modeling of the viscosities and densities of mixtures involving 1-methylnaphthalene, providing valuable data for industrial applications and theoretical studies in chemical engineering (Tenorio et al., 2024).

  • Chemical Composition and Optical Properties of Secondary Organic Aerosol from Photooxidation of Volatile Organic Compound Mixtures.: Investigates the secondary organic aerosols produced from photooxidation of volatile organic compounds including 1-methylnaphthalene, highlighting their optical properties and implications for air quality and climate modeling (Cui et al., 2024).

  • Oxidation 1-methyl naphthalene based on the synergy of environmentally persistent free radicals (EPFRs) and PAHs in particulate matter (PM) surface.: This study explores the oxidative mechanisms of 1-methyl naphthalene on particulate matter surfaces, facilitated by environmentally persistent free radicals. The findings contribute to the understanding of air pollution chemistry and environmental degradation processes (Ghimire et al., 2023).

Esclusione di responsabilità

For R&D or non-EU Food use. Not for retail sale.

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 4 Oral - Aquatic Chronic 2 - Asp. Tox. 1

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

179.6 °F - closed cup

Punto d’infiammabilità (°C)

82 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Identification of volatile organic compounds in the manures of cow, hog and chicken by solid phase microextraction coupled with gas chromatography/mass spectrometry
Huang J, et al.
Sepu, 25(3), 425-429 (2007)
Volatile organic compounds and particulates as components of diesel engine exhaust gas.
Schulz H, et al.
Combustion and Flame, 118(1), 179-190 (1999)
Determination of the volatile composition in brown millet, milled millet and millet bran by gas chromatography/mass spectrometry.
Liu J, et al.
Molecules (Basel), 17(3), 2271-2282 (2012)
Volatile compounds of raw spirits from different distilling stages of Luzhou-flavor spirit
Zheng, Jia, et al
Food Science and Technology Research, 20(2), 283-293 (2014)
Mykola Seredych et al.
Langmuir : the ACS journal of surfaces and colloids, 26(1), 227-233 (2009-12-30)
Two synthetic, polymer-derived carbons were modified with urea to incorporate nitrogen surface functional groups. Then they were investigated as adsorbents of dibenzothiophene (DBT) and 4, 6-dimethyldibenzothiophene (DMDBT) from simulated diesel fuel under dynamic conditions with the total concentration of sulfur

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