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557811

Sigma-Aldrich

2,4-Diisopropylphenol

98%

Sinônimo(s):

2,4-Bis(1-methylethyl)phenol, 2,4-Bis(propan-2-yl)phenol, 2,4-Di(propan-2-yl)phenol

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About This Item

Fórmula linear:
[(CH3)2CH]2C6H3OH
Número CAS:
2934-05-6
Peso molecular:
178.27
Número CE:
220-906-1
Número MDL:
MFCD01707536
Código UNSPSC:
12352100
ID de substância PubChem:
24879699
NACRES:
NA.22

Ensaio

98%

índice de refração

n20/D 1.5130 (lit.)

pb

79-80 °C (lit.)

densidade

0.948 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CC(C)c1ccc(O)c(c1)C(C)C

InChI

1S/C12H18O/c1-8(2)10-5-6-12(13)11(7-10)9(3)4/h5-9,13H,1-4H3

chave InChI

KEUMBYCOWGLRBQ-UHFFFAOYSA-N

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Descrição geral

2,4-Diisopropylphenol, commonly known as 2,4-propofol, is an isomeric form of propofol. EC50 Microtox (5min, 25°C) assay value of 2,4-diisopropylphenol is 2x10-4mM. It is formed as one of the reaction products from the reaction between boron fluoride with isopropyl phenyl ether.

Aplicação

2,4-Diisopropylphenol may be used in the preparation of N,N-bis(3,5-diisopropyl-2-hydroxybenyl)-N′,N′-dimethyl-1,2-diaminoethane.

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H319,H335

Classificações de perigo

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

230.0 °F - closed cup

Ponto de fulgor (°C)

110 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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Organic Reactions with Boron Fluoride. V. The Rearrangement of Isopropylphenol, o-, m-and p-Cresyl Ethers.
Sowa FJ, et al.
Journal of the American Chemical Society, 55(8), 3402-3407 (1933)
rac-Lactide polymerization using aluminum complexes bearing tetradentate phenoxy-amine ligands.
Tang Z and Gibson VC.
European Polymer Journal, 43(1), 150-155 (2007)
Shanker Karunanithi et al.
eNeuro, 7(1) (2020-02-06)
Propofol is the most common general anesthetic used for surgery in humans, yet its complete mechanism of action remains elusive. In addition to potentiating inhibitory synapses in the brain, propofol also impairs excitatory neurotransmission. We use electrophysiological recordings from individual
T P Heil et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 24(4), 349-360 (1989-08-01)
EC50 Microtox (5 min, 25 degrees C) assay values for 2-isopropylphenol, 3-isopropylphenol, 4-isopropylphenol, 2,4-diisopropylphenol, 2,5-diisopropylphenol 2,6-diisopropylphenol, 3,5-diisopropylphenol, carvacrol, thymol, thiophenol, and thiocresol ranged from 2 x 10(-2) mM for thymol (least toxic) to 2 x 10(-4) mM for 2,4-diisopropylphenol and
Tomoaki Urabe et al.
European journal of pharmacology, 884, 173303-173303 (2020-07-19)
Propofol, most frequently used as a general anesthetic due to its versatility and short-acting characteristics, is thought to exert its anesthetic actions via GABAA receptors; however, the precise mechanisms of its adverse action including angialgia remain unclear. We examined the
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