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Supelco

1,4-Dimethylnaphthalene

analytical standard

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About This Item

Fórmula linear:
C10H6(CH3)2
Número CAS:
571-58-4
Peso molecular:
156.22
Beilstein:
2039842
Número CE:
209-335-9
Número MDL:
MFCD00004037
Código UNSPSC:
41116107
ID de substância PubChem:
329755705

grau

analytical standard

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

índice de refração

n20/D 1.613 (lit.)

pb

262-264 °C/751 mmHg (lit.)

pf

−18 °C (lit.)

densidade

1.016 g/mL at 25 °C (lit.)

aplicação(ões)

environmental

formato

neat

cadeia de caracteres SMILES

Cc1ccc(C)c2ccccc12

InChI

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

chave InChI

APQSQLNWAIULLK-UHFFFAOYSA-N

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Aplicação

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Palavra indicadora

Danger

Frases de perigo

H302,H304,H319,H410

Classificações de perigo

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 3 - Asp. Tox. 1 - Eye Irrit. 2

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

235.4 °F - closed cup

Ponto de fulgor (°C)

113 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves

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Certificados de análise (COA)

Lot/Batch Number
BCCK0717
BCBZ5225
SZBE010XV
SZB9029XV
SZE9029X

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Damir Posavec et al.
Organic & biomolecular chemistry, 10(35), 7062-7069 (2012-08-01)
Decomposition of endoperoxide containing molecules is an attractive approach for the delayed release of singlet oxygen under mild reaction conditions. Here we describe a new method for the adaptation of the corresponding decay times by controlling the supramolecular functional structure
Michael A Campbell et al.
Functional & integrative genomics, 12(3), 533-541 (2011-11-25)
The suppression of sprout growth is critical for the long-term storage of potato tubers. 1,4-Dimethylenapthlene (DMN) is a new class of sprout control agent but the metabolic mode of action for this compound has yet to be elucidated. Changes in
D S Malament et al.
Carcinogenesis, 2(8), 723-729 (1981-01-01)
Phenanthrene (Phe) and to a lesser degree 1,4-dimethylnaphthalene (DMeN) were each found to retard the development of epidermoid carcinomas in hamster buccal pouch induced by the thrice weekly application of a 0.5 per cent solution of 7,12-dimethylbenz[a]anthracene (DMBA) in heavy
A Kilanowicz et al.
International journal of occupational medicine and environmental health, 13(4), 325-334 (2001-03-30)
The distribution, excretion and metabolism of 1,4-dimethylnaphthalene following i.p. administration of a single dose of 28 mg/kg to rats, was investigated using radiotracer [3H] and gas chromatography-mass spectrometry technique (GC-MS). After 72 h, about 97% of the given dose was
P Di Mascio et al.
Biological chemistry Hoppe-Seyler, 376(5), 297-301 (1995-05-01)
Carotenoids comprise one of the most widespread classes of pigments found in nature. Polyene pigments from the dinoflagellate Gonyaulax polyedra were extracted every hour over a 24 hour period and the levels of beta-carotene during the day-phase were found to
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