1.04727

2,2,4-Trimetilpentano

for analysis EMSURE^® ACS,Reag. Ph Eur

• Sinónimos: Isooctano
• Fórmula lineal: (CH₃)₂CHCH₂C(CH₃)₃
• Número de CAS: 540-84-1
• Peso molecular: 114.23
• Beilstein: 1696876
• Número MDL: MFCD00008943
• Código UNSPSC: 12191502
• Número índice de la CE: 208-759-1
• NACRES: NB.21

Propiedades

• grado: ACS reagent
• Nivel de calidad: 300
• Agency: reag. Ph. Eur.
• densidad de vapor: 3.9 (vs air)
• presión de vapor: 41 mmHg ( 21 °C)
• Línea del producto: EMSURE^®
• Análisis: ≥99.5% (GC)
• formulario: liquid
• temp. de autoignición: 745 °F
• potencia: >2500 mg/kg LD₅₀, oral (Rat)
• lim. expl.: 6 %
• impurezas: ≤0.0003 meq/g Acidity; ≤0.005% Sulfur compounds (as S); ≤0.01% Water
• residuo de evap.: ≤0.001%
• color: APHA: ≤10
• transmitancia: 250-420 nm, ≥98%
• índice de refracción: n20/D 1.391 (lit.)
• pH: 7
• bp: 98-99 °C (lit.)
• mp: −107 °C (lit.)
• temperatura de transición: flash point -12 °C
• densidad: 0.692 g/mL at 25 °C (lit.)
• trazas de catión: Al: ≤0.00005%; B: ≤0.000002%; Ba: ≤0.00001%; Ca: ≤0.00005%; Cd: ≤0.000005%; Co: ≤0.000002%; Cr: ≤0.000002%; Cu: ≤0.000002%; Fe: ≤0.00001%; Mg: ≤0.00001%; Mn: ≤0.000002%; Ni: ≤0.000002%; Pb: ≤0.00001%; Sn: ≤0.00001%; Zn: ≤0.00001%
• temp. de almacenamiento: 2-30°C
• cadena SMILES: CC(C)CC(C)(C)C
• InChI: 1S/C8H18/c1-7(2)6-8(3,4)5/h7H,6H2,1-5H3
• Clave InChI: NHTMVDHEPJAVLT-UHFFFAOYSA-N

Descripción

Aplicación

• Behavior of acetyl modified amino acids in reverse micelles: a non-invasive and physiochemical approach.: This study utilizes isooctane in reverse micelles to explore the behavior of acetyl modified amino acids. The findings emphasize isooctane′s role in facilitating non-invasive and physiochemical analyses, highlighting its importance in analytical chemistry and biochemical studies (Mehta et al., 2007).


• Nonionic surfactants: a key to enhance the enzyme activity at cationic reverse micellar interface.: The research investigates the use of isooctane in forming cationic reverse micelles with nonionic surfactants to enhance enzyme activity. Isooctane′s effectiveness in this context underscores its value in biocatalysis and enzymatic studies (Shome et al., 2007).


• Lecithin organogels used as bioactive compounds carriers. A microdomain properties investigation.: This study explores the application of isooctane in lecithin organogels for carrying bioactive compounds. Isooctane′s role in stabilizing the microdomains within the organogels is crucial for their effectiveness in drug delivery systems (Avramiotis et al., 2007).


• Switching electrical conductivity in an AOT-isooctane-water microemulsion through photodimerization of solubilized N-methyl-2-quinolone.: This research demonstrates the use of isooctane in AOT-water microemulsions to switch electrical conductivity via photodimerization. The study highlights isooctane′s utility in developing responsive materials for advanced chemical and physical applications (Bufe and Wolff, 2006).


• Photochromism of crown ethers with incorporated azobenzene moiety.: Isooctane is utilized in studying the photochromism of crown ethers with azobenzene moieties. The findings underscore isooctane′s role in facilitating the investigation of photoresponsive materials, relevant to materials science and photochemistry (Janus and Sworakowski, 2005).

Nota de análisis

Purity (GC): ≥ 99.5 %
Identity (IR): conforms
Color: ≤ 10 Hazen
Acidity: ≤ 0.0003 meq/g
Density (d 20 °C/20 °C): 0.691 - 0.696
Refractive index (n 20/D): 1.391 - 1.393
Boiling range (98-100°C): ≥ 95 % (v/v)
Sulfur compounds (as S): ≤ 0.005 %
Readily carbonizable substances: conforms
Transmission (between 250nm and 420nm): ≥ 98 %
Al (Aluminium): ≤ 0.00005 %
B (Boron): ≤ 0.000002 %
Ba (Barium): ≤ 0.00001 %
Ca (Calcium): ≤ 0.00005 %
Cd (Cadmium): ≤ 0.000005 %
Co (Cobalt): ≤ 0.000002 %
Cr (Chromium): ≤ 0.000002 %
Cu (Copper): ≤ 0.000002 %
Fe (Iron): ≤ 0.00001 %
Mg (Magnesium): ≤ 0.00001 %
Mn (Manganese): ≤ 0.000002 %
Ni (Nickel): ≤ 0.000002 %
Pb (Lead): ≤ 0.00001 %
Sn (Tin): ≤ 0.00001 %
Zn (Zinc): ≤ 0.00001 %
Evaporation residue: ≤ 0.001 %
Water: ≤ 0.01 %
Corresponds to ACS, Ph Eur-reagent

Información legal

EMSURE is a registered trademark of Merck KGaA, Darmstadt, Germany

Información de seguridad

• Pictogramas: GHS02,GHS07,GHS08,GHS09
• Palabra de señalización: Danger
• Frases de peligro: H225 - H304 - H315 - H336 - H410
• Consejos de prudencia: P210 - P233 - P273 - P301 + P310 - P303 + P361 + P353 - P331
• Clasificaciones de peligro: Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3
• Órganos de actuación: Central nervous system
• Código de clase de almacenamiento: 3 - Flammable liquids
• Clase de riesgo para el agua (WGK): WGK 2
• Punto de inflamabilidad (°F): 10.4 °F - closed cup
• Punto de inflamabilidad (°C): -12 °C - closed cup