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Merck

LM2000

Avanti

Sphingosine (d17:1)

Avanti Research - A Croda Brand LM2000, ethanol solution

Synonym(e):

heptadeca-sphing-4-enine

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About This Item

Empirische Formel (Hill-System):
C17H35NO2
CAS-Nummer:
Molekulargewicht:
285.47
UNSPSC-Code:
12352211
NACRES:
NA.25

Form

ethanol solution

Verpackung

pkg of 1 × 1 mL (LM2000-1EA)

Hersteller/Markenname

Avanti Research - A Croda Brand LM2000

Konzentration

~10 μg/mL (Refer to C of A for lot specific concentration.)

Versandbedingung

dry ice

Lagertemp.

−20°C

SMILES String

OC[C@@](N)([H])[C@]([H])(O)/C=C/CCCCCCCCCCCC

InChI

1S/C17H35NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-17(20)16(18)15-19/h13-14,16-17,19-20H,2-12,15,18H2,1H3/b14-13+/t16-,17+/m0/s1

InChIKey

RBEJCQPPFCKTRZ-LHMZYYNSSA-N

Anwendung

Sphingosine (d17:1) or heptadeca-sphing-4-enine might be used as an internal standard for the identification of long chain bases (LCBs) in Colletotrichum gloeosporioides mycelia. It is also used as an internal standard for sample preparation and LC-MS/MS analysis for sphingolipids.

Verpackung

2 mL Amber Glass Sealed Ampule (LM2000-1EA)

Rechtliche Hinweise

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Piktogramme

FlameExclamation mark

Signalwort

Danger

H-Sätze

Gefahreneinstufungen

Eye Irrit. 2 - Flam. Liq. 2

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 1

Flammpunkt (°F)

55.4 °F - closed cup

Flammpunkt (°C)

13.0 °C - closed cup


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Fungal glucosylceramide plays important role in cell division, hyphal formation and growth, spore germination and the modulation of virulence and has recently been considered as target for small molecule inhibitors. In this study, we characterized CgGCS, a protein encoding a
Christopher M Adams et al.
The Journal of biological chemistry, 279(50), 52772-52780 (2004-09-29)
The current paper demonstrates that cholesterol and its hydroxylated derivative, 25-hydroxycholesterol (25-HC), inhibit cholesterol synthesis by two different mechanisms, both involving the proteins that control sterol regulatory element-binding proteins (SREBPs), membrane-bound transcription factors that activate genes encoding enzymes of lipid
Claudia Rossi et al.
International journal of molecular sciences, 19(11) (2018-11-18)
Multiple sclerosis (MuS) is an autoimmune disease of the central nervous system characterized by neuroinflammation, neurodegeneration, and degradation of the myelin sheath. Epidemiological studies have shown that the female gender is more susceptible than the male gender to MuS development
Veera Venkata Ratnam Bandaru et al.
BMC neuroscience, 15, 137-137 (2014-12-30)
Cholesterol metabolism is important for the maintenance of myelin and neuronal membranes in the central nervous system. Blood concentrations of the brain specific cholesterol metabolite 24S-hydroxysterol to the peripheral metabolite 27-hydroxycholesterol may be useful surrogate markers for neurodegenerative diseases including
Rosamaria Lappano et al.
PloS one, 6(1), e16631-e16631 (2011-02-10)
The hydroxylated derivatives of cholesterol, such as the oxysterols, play important roles in lipid metabolism. In particular, 25-hydroxycholesterol (25 HC) has been implicated in a variety of metabolic events including cholesterol homeostasis and atherosclerosis. 25 HC is detectable in human

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