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Merck

74158

Supelco

Nonadecane

analytical standard

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About This Item

Fórmula lineal:
CH3(CH2)17CH3
Número de CAS:
Peso molecular:
268.52
Beilstein:
1742892
Número MDL:
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
NACRES:
NA.24

grado

analytical standard

Nivel de calidad

densidad de vapor

9.27 (vs air)

presión de vapor

1 mmHg ( 133.2 °C)

Análisis

≥99.5% (GC)

temp. de autoignición

446 °F

caducidad

limited shelf life, expiry date on the label

técnicas

HPLC: suitable
gas chromatography (GC): suitable

bp

330 °C (lit.)

mp

30-34 °C (lit.)
32-34 °C

densidad

0.786 g/mL at 25 °C (lit.)

aplicaciones

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

formato

neat

cadena SMILES

CCCCCCCCCCCCCCCCCCC

InChI

1S/C19H40/c1-3-5-7-9-11-13-15-17-19-18-16-14-12-10-8-6-4-2/h3-19H2,1-2H3

Clave InChI

LQERIDTXQFOHKA-UHFFFAOYSA-N

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Aplicación

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

Productos 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.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

212.0 °F - closed cup

Punto de inflamabilidad (°C)

100 °C - closed cup

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)


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Certificados de análisis (COA)

Lot/Batch Number

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Los clientes también vieron

C Pidgeon et al.
Analytical biochemistry, 181(1), 28-32 (1989-08-15)
Quantitating the lipid content in organic lipid solutions and extracted membrane preparations is described. Fourier transform infrared analysis of thin films using perdeuterated nonadecane as an internal standard permitted quantitation with greater than 95% accuracy.
Stefano Colazza et al.
Die Naturwissenschaften, 96(8), 975-981 (2009-05-21)
Chemical footprints left behind by true bugs are perceived as contact kairomones by scelionid egg parasitoids. Female wasps encountering a contaminated artificial substrate display a characteristic arrestment posture, holding the body motionless and antennating the surface. In the system Nezara
Abdiwahab A Musse et al.
The Journal of biological chemistry, 281(2), 885-895 (2005-11-22)
Helix 1 of the membrane-associated closed state of the colicin E1 channel domain was studied by site-directed fluorescence labeling where bimane was covalently attached to a single cysteine residue in each mutant protein. A number of fluorescence properties of the
Stefano Colazza et al.
Journal of chemical ecology, 33(7), 1405-1420 (2007-05-18)
Contact kairomones from adult southern green stink bugs, Nezara viridula (L.) (Heteroptera: Pentatomidae) that elicit foraging behavior of the egg parasitoid Trissolcus basalis (Wollaston) were investigated in laboratory experiments. Chemical residues from tarsi and scutella of N. viridula induced foraging
Daniela Lo Giudice et al.
Journal of chemical ecology, 37(6), 622-628 (2011-05-07)
Egg parasitoids are able to find their hosts by exploiting their chemical footprints as host location cues. In nature, the apolar epicuticular wax layer of plants that consists of several classes of hydrocarbons serves as the substrate that retains these

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