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18629

Sigma-Aldrich

3-Methyl-3-butenyl-phosphat Dilithiumsalz

≥95.0% (TLC)

Synonym(e):

Isopentenyl-phosphat Dilithiumsalz, Phosphorsäure-mono-(3-methyl-3-butenylester) Dilithiumsalz

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About This Item

Empirische Formel (Hill-System):
C5H9Li2O4P
CAS-Nummer:
18687-42-8
Molekulargewicht:
177.98
Beilstein:
4339123
MDL-Nummer:
MFCD17215949
UNSPSC-Code:
12352106
PubChem Substanz-ID:
329751724
NACRES:
NA.25

Qualitätsniveau

100

Assay

≥95.0% (TLC)

Verunreinigungen

≤10.0% water

Lagertemp.

−20°C

SMILES String

[Li+].[Li+].CC(=C)CCOP([O-])([O-])=O

InChI

1S/C5H11O4P.2Li/c1-5(2)3-4-9-10(6,7)8;;/h1,3-4H2,2H3,(H2,6,7,8);;/q;2*+1/p-2

InChIKey

ACAZFVVXIFTWMF-UHFFFAOYSA-L

Anwendung

Isopentenyl phosphate may be used as a substrate to study the characteristics and kinetics of isopentenyl phosphate kinases.

Biochem./physiol. Wirkung

Isopentenyl monophosphate is phosphorylated into isopentenyl pyrophosphate at very low rates.

Verpackung

Bottomless glass bottle. Contents are inside inserted fused cone.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Analysenzertifikate (COA)

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Mark F Mabanglo et al.
Biochemistry, 51(4), 917-925 (2011-12-14)
Isopentenyl phosphate kinase (IPK) catalyzes the phosphorylation of isopentenyl phosphate to form the isoprenoid precursor isopentenyl diphosphate in the archaeal mevalonate pathway. This enzyme is highly homologous to fosfomycin kinase (FomA), an antibiotic resistance enzyme found in a few strains
C Donninger et al.
The Biochemical journal, 105(2), 545-547 (1967-11-01)
1. Isopentenol was converted into isopentenyl phosphate with phosphoryl chloride in ether containing pyridine. 2. The isopentenyl phosphate reacted in 2-methylpropan-2-ol-water with morpholine and dicyclohexylcarbodi-imide to give isopentenyl phosphoromorpholidate. 3. The isopentenyl phosphoromorpholidate, with inorganic phosphate in pyridine containing tributylamine
Nikki Dellas et al.
ACS chemical biology, 5(6), 589-601 (2010-04-16)
The biosynthesis of isopentenyl diphosphate (IPP) from either the mevalonate (MVA) or the 1-deoxy-d-xylulose 5-phosphate (DXP) pathway provides the key metabolite for primary and secondary isoprenoid biosynthesis. Isoprenoid metabolism plays crucial roles in membrane stability, steroid biosynthesis, vitamin production, protein
Mark F Mabanglo et al.
ACS chemical biology, 7(7), 1241-1246 (2012-04-27)
Isopentenyl phosphate kinase (IPK) catalyzes the ATP-dependent phosphorylation of isopentenyl phosphate (IP) to form isopentenyl diphosphate (IPP) during biosynthesis of isoprenoid metabolites in Archaea. The structure of IPK from the archeaon Thermoplasma acidophilum (THA) was recently reported and guided the
Mo Chen et al.
Biochemistry, 49(1), 207-217 (2009-11-26)
Archaea synthesize isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), the essential building blocks of isoprenoid compounds, from mevalonate (MVA). However, an analysis of the genomes of several members of the Archaea failed to identify genes for the enzymes required to

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