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30039

Supelco

p-Cymene

analytical standard

Sinônimo(s):

1-Isopropyl-4-methylbenzene, 4-Isopropyltoluene

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About This Item

Fórmula linear:
CH3C6H4CH(CH3)2
Número CAS:
99-87-6
Peso molecular:
134.22
Beilstein:
1903377
Número CE:
202-796-7
Número MDL:
MFCD00008893
Código UNSPSC:
41116107
ID de substância PubChem:
329753413
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

densidade de vapor

4.62 (vs air)

pressão de vapor

1.5 mmHg ( 20 °C)
3.7 mmHg ( 37.7 °C)

Ensaio

≥99.5% (GC)

temperatura de autoignição

817 °F

prazo de validade

limited shelf life, expiry date on the label

Lim. expl.

5.6 %

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

índice de refração

n20/D 1.490 (lit.)
n20/D 1.491

pb

176-178 °C (lit.)

densidade

0.86 g/mL at 25 °C (lit.)

aplicação(ões)

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

formato

neat

cadeia de caracteres SMILES

CC(C)c1ccc(C)cc1

InChI

1S/C10H14/c1-8(2)10-6-4-9(3)5-7-10/h4-8H,1-3H3

chave InChI

HFPZCAJZSCWRBC-UHFFFAOYSA-N

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Categorias relacionadas

Aplicação

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

Outras notas

This compound is commonly found in plants of the genus: thymus

Produtos recomendados

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 3 Inhalation - Aquatic Chronic 2 - Asp. Tox. 1 - Flam. Liq. 3 - Repr. 2

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

125.6 °F - closed cup

Ponto de fulgor (°C)

52 °C - closed cup

Equipamento de proteção individual

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

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
BCCH0770
BCCG4236
BCCG4235
BCCB7812
BCCB4998

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Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

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Lydia E H Paul et al.
Inorganic chemistry, 51(2), 1057-1067 (2012-01-10)
The relative affinity of the cationic triangular metallaprism, [(pCH(3)C(6)H(4)Pr(i))(6)Ru(6)(tpt)(2)(dhbq)(3)](6+) ([1](6+)), for various amino acids, ascorbic acid, and glutathione (GSH) has been studied at 37 °C in aqueous solutions at pD 7, using NMR spectroscopy and electrospray ionization mass spectrometry (ESI-MS).
Vanessa Kar-Yan Lo et al.
Journal of the American Chemical Society, 134(18), 7588-7591 (2012-04-26)
Complex [(p-cymene)Ru(η(1)-O(2)CCF(3))(2)(OH(2))] mediated transformation of α-diazoacetamides ArCH(2)N(C(CH(3))(3))C(O)CHN(2) to result in carbene insertion into the primary C-H bond exclusively, with the γ-lactam products being isolated in up to 98% yield. This unexpected reaction is striking in view of the presence of
Natalia Busto et al.
Chemistry, an Asian journal, 7(4), 788-801 (2012-02-07)
The reactions of two diaminotriazine ligands 2,4-diamino-6-(2-pyridyl)-1,3,5-triazine (2-pydaT) and 6-phenyl-2,4-diamino-1,3,5-triazine (PhdaT) with ruthenium-arene precursors led to a new family of ruthenium(II) compounds that were spectroscopically characterized. Four of the complexes were cationic, with the general formula [(η(6)-arene)Ru(κ(2)-N,N-2-pydaT)Cl]X (X=BF(4), TsO; arene=p-cymene:
Lutz Ackermann et al.
Organic letters, 14(8), 2146-2149 (2012-04-13)
The ruthenium(II) carboxylate complex [Ru(O(2)CMes)(2)(p-cymene)] enabled efficient direct arylations of unactivated C-H bonds with easily available, inexpensive phenols. Extraordinary chemoselectivity of the well-defined ruthenium catalyst set the stage for challenging C-H/C-O bond functionalizations to occur under solvent-free conditions as well
Kenichi Ogata et al.
Dalton transactions (Cambridge, England : 2003), 42(7), 2362-2365 (2012-12-14)
A series of 1,2,3-triazol-5-ylidene (tzNHC) complexes of a (p-cymene)ruthenium system was synthesized. The reactivity of the N-bonded and C-bonded aryl groups in the tzNHC ligand was found to be significantly different with respect to intramolecular aromatic C-H bond activation.
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