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76532

Sigma-Aldrich

Geranyl pyrophosphate lithium salt

≥95.0% (TLC)

Synonym(s):

(E)-3,7-Dimethyl-2,6-octadien-1-ol trihydrogen pyrophosphate lithium salt, (E)-3,7-Dimethyl-2,6-octadien-1-yl pyrophosphate lithium salt, GPP-Li

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About This Item

Empirical Formula (Hill Notation):
C10H20O7P2 · xLi+
CAS Number:
21141-43-5
Molecular Weight:
314.21 (free acid basis)
Beilstein:
1915690
MDL number:
MFCD18827619
UNSPSC Code:
85151701
NACRES:
NA.25
grade:
for analytical purposes
form:
powder
Pricing and availability is not currently available.

grade

for analytical purposes

Assay

≥95.0% (TLC)

form

powder

storage temp.

−20°C

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Related Categories

Biochem/physiol Actions

Metabolite in monoterpenoid biosynthesis, substrate for monoterpene synthases.[1]

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

76532-50MG:
76532-VAR:
76532-BULK:
76532-10MG:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCD9105
BCBW7840
BCBD0052V
BCBD0052

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F Pont et al.
Analytical chemistry, 73(15), 3562-3569 (2001-08-21)
New phosphorylated microbial metabolites referred to as phosphoantigens activate immune responses in humans. Although these molecules have leading applications in medical research, no direct method allows their rapid and unambiguous structural identification. Here, we interfaced online HPAEC (high performance anion-exchange
V G Ladygin
Zhurnal obshchei biologii, 63(4), 299-325 (2002-09-27)
The author discusses the current state of biochemical and genetic aspects of carotenoid biosynthesis in chloroplasts of algae and higher plants. Two ways of biosynthesis of key C5-isoperene units have been considered: 1) from acetate (C2) via mevalonic acid (C6)
Ravi S Singh et al.
BMC molecular biology, 11, 88-88 (2010-11-26)
Geranyl pyrophosphate (GPP) and p-hydroxybenzoate (PHB) are the basic precursors involved in shikonins biosynthesis. GPP is derived from mevalonate (MVA) and/or 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway(s), depending upon the metabolite and the plant system under consideration. PHB, however, is synthesized by
Orapin Ariyawutthiphan et al.
Acta crystallographica. Section D, Biological crystallography, 68(Pt 11), 1558-1569 (2012-10-24)
In the typical isoprenoid-biosynthesis pathway, condensation of the universal C(5)-unit precursors isopentenyl pyrophosphate (IPP) and dimethylallyl pyrophosphate (DMAPP) occurs via the common intermediates prenyl pyrophosphates (C(10)-C(20)). The diversity of isoprenoids reflects differences in chain length, cyclization and further additional modification
Sarah A Holstein et al.
Lipids, 39(4), 293-309 (2004-09-11)
The isoprenoid biosynthetic pathway is the source of a wide array of products. The pathway has been highly conserved throughout evolution, and isoprenoids are some of the most ancient biomolecules ever identified, playing key roles in many life forms. In
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