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360740

Sigma-Aldrich

1,2-Dimethylnaphthalene

95%

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About This Item

Formula condensata:
C10H6(CH3)2
Numero CAS:
573-98-8
Peso molecolare:
156.22
Beilstein:
2039376
Numero CE:
209-364-7
Numero MDL:
MFCD00004035
Codice UNSPSC:
12352100
ID PubChem:
24861997
NACRES:
NA.22

Saggio

95%

Indice di rifrazione

n20/D 1.615 (lit.)

P. ebollizione

266-267 °C (lit.)

Punto di fusione

−2-−1 °C (lit.)

Densità

1.013 g/mL at 25 °C (lit.)

Stringa SMILE

Cc1ccc2ccccc2c1C

InChI

1S/C12H12/c1-9-7-8-11-5-3-4-6-12(11)10(9)2/h3-8H,1-2H3
QNLZIZAQLLYXTC-UHFFFAOYSA-N

Informazioni sul gene

human ... CYP1A2(1544)

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Descrizione generale

1,2-Dimethylnaphthalene is a polycyclic aromatic hydrocarbon. Its effect on the naupliar and adult stages of the marine cyclopoid copepod Oithona davisae is reported.

Applicazioni

1,2-Dimethylnaphthalene is suitable reagent used to investigate the secondary organic aerosol (SOA) production via gas-phase photooxidation.

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

235.4 °F - closed cup

Punto d’infiammabilità (°C)

113 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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Certificati d'analisi (COA)

Lot/Batch Number
05905LWV
05905LW

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2-Methylnaphthalene (β) 95%

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Secondary organic aerosol formation from photooxidation of naphthalene and alkylnaphthalenes: implications for oxidation of intermediate volatility organic compounds (IVOCs).
Chan AWH, et al.
Atmospheric Chemistry and Physics, 9(9), 3049-3060 (2009)
Enric Saiz et al.
Environmental pollution (Barking, Essex : 1987), 157(4), 1219-1226 (2009-01-17)
Short-term (24h) exposure experiments have been conducted to determine the effects of two environmental relevant polycyclic aromatic hydrocarbons (PAHs), naphthalene (NAPH) and dimethylnaphthalene (C2-NAPH), on the naupliar and adult stages of the marine cyclopoid copepod Oithona davisae. To resemble more
A Kilanowicz et al.
International journal of occupational medicine and environmental health, 11(4), 305-317 (1999-02-24)
The aim of this study was to investigate the distribution, excretion and metabolism of 1,2-dimethylnaphthalene-[ring-U-3H] in rats. The experiments were performed on 54 male outbred IMP:Wist rats with body weight of 200 g +/- 20%. The compound was given i.p.
Nien-Hsin Kao et al.
Marine pollution bulletin, 97(1-2), 319-332 (2015-06-08)
Three fishing harbors were investigated to study the polycyclic aromatic hydrocarbons in the sediments and trace possible anthropogenic sources by identification of cyclic terpenoid biomarkers. Seventeen terpanes, 10 steranes and 10 bicyclic sesquiterpanes in the marine diesel and the three
Kunal Roy et al.
European journal of medicinal chemistry, 44(5), 1941-1951 (2008-12-27)
A series of naphthalene and non-naphthalene derivatives (n=42) having cytochrome P450 2A6 and 2A5 inhibitory activities, reported by Rahnasto et al., were subjected to QSAR and QAAR studies. The analyses were performed using electronic, spatial, shape and thermodynamic descriptors to
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