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Merck

C6072

Sigma-Aldrich

Cholesterinpalmitat

≥98% (HPLC; detection at 205 nm)

Synonym(e):

Cholesterin-hexandecanoat

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About This Item

Empirische Formel (Hill-System):
C43H76O2
CAS-Nummer:
Molekulargewicht:
625.06
Beilstein:
2342867
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352211
PubChem Substanz-ID:
NACRES:
NA.77

Biologische Quelle

synthetic (organic)

Assay

≥98% (HPLC; detection at 205 nm)

Form

powder

mp (Schmelzpunkt)

74-77 °C (lit.)

Funktionelle Gruppe

ester

Versandbedingung

ambient

Lagertemp.

−20°C

SMILES String

CCCCCCCCCCCCCCCC(=O)O[C@H]1CC[C@]2(C)C3CC[C@]4(C)C(CCC4C3CC=C2C1)[C@H](C)CCCC(C)C

InChI

1S/C43H76O2/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-23-41(44)45-36-28-30-42(5)35(32-36)24-25-37-39-27-26-38(34(4)22-20-21-33(2)3)43(39,6)31-29-40(37)42/h24,33-34,36-40H,7-23,25-32H2,1-6H3/t34-,36+,37+,38-,39+,40+,42+,43-/m1/s1

InChIKey

BBJQPKLGPMQWBU-JADYGXMDSA-N

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Verwandte Kategorien

Anwendung

Cholesteryl palmitate was used as standard in HPLC analysis of lipids from cooked ground beef and rat liver and mouse muscle tissue samples.

Biochem./physiol. Wirkung

Cholesteryl palmitate was used as standard in HPLC analysis of lipids from cooked ground beef and rat liver and mouse muscle tissue samples.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


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Kunden haben sich ebenfalls angesehen

K Owens et al.
Journal of lipid research, 11(5), 486-495 (1970-09-01)
Myofibrillar, mitochondrial, and microsomal fractions were prepared from normal and dystrophic mouse limb muscle by differential centrifugation and analyzed for phospholipids and cholesterol. Fatty acids and aldehydes of neutral lipids and of phospholipids from whole muscle and particulate fractions were
TBA Values and 7?Ketocholesterol in Refrigerated Raw and Cooked Ground Beef
Vore VR
Journal of Food Science, 53, 1058-1061 (1988)
7-Ketocholesterol. Its effects on hepatic cholesterogenesis and its hepatic metabolism in vivo and in vitro.
S K Erickson et al.
The Journal of biological chemistry, 252(15), 5186-5193 (1977-08-10)
A L MacKay et al.
Biochimica et biophysica acta, 601(1), 22-33 (1980-09-02)
Dispersions (50 wt% in water) of sphingomyelin/cholesteryl palmitate (95 : 5 mol%) have been studied by 2H- and 31P-NMR spectroscopy between 25 and 60 degrees C. The deuterated esters, cholesteryl palmitate-d31 and cholesteryl palmitate-16, 16, 16-d3, were used for 2H-NMR
J P Despres et al.
The American journal of physiology, 254(5 Pt 1), E667-E675 (1988-05-01)
In humans, high-density lipoprotein (HDL)-cholesterol ester turnover exceeds that of HDL apoproteins by severalfold or more, suggesting an independent catabolic fate of these constituents. The present study investigated the cellular uptake and dissociation of HDL labeled in its apoproteins with

Artikel

Cholesterol undergoes esterification to improve transport. Cholesterol esters are more easily packaged into the interior of lipoproteins - increasing the quantity that can be readily transported in the blood stream.

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