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Merck
CN

54747

γ,γ-Dimethylallyl phosphate ammonium salt

≥93.0% (TLC)

Synonym(s):

3,3-Dimethylallyl phosphate ammonium salt, 3-Methyl-2-butenyl phosphate ammonium salt, Phosphoric acid mono-(3-methyl-2-butenyl ester) ammonium salt, Prenyl phosphate ammonium salt

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About This Item

Empirical Formula (Hill Notation):
C5H11O4P · xNH3
Molecular Weight:
166.11 (free acid basis)
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352106
MDL number:
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Product Name

γ,γ-Dimethylallyl phosphate ammonium salt, ≥93.0% (TLC)

InChI key

FLEGYDAACQHRAY-UHFFFAOYSA-N

SMILES string

N.C\C(C)=C\COP(O)(O)=O

InChI

1S/C5H11O4P.H3N/c1-5(2)3-4-9-10(6,7)8;/h3H,4H2,1-2H3,(H2,6,7,8);1H3

assay

≥93.0% (TLC)

storage temp.

−20°C

Quality Level

Application

Gamma, gamma-dimethylallyl phosphate may be useful in studies of the archaeal isopentenyl phosphate kinases.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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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
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

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