Sign In to View Organizational & Contract Pricing.
About This Item
Empirical Formula (Hill Notation):
C10H20O7P2 · xLi+
CAS Number:
Molecular Weight:
314.21 (free acid basis)
MDL number:
UNSPSC Code:
85151701
NACRES:
NA.25
Beilstein/REAXYS Number:
1915690
Assay:
≥95.0% (TLC)
Form:
powder
Skip To
Looking for similar products? Visit Product Comparison Guide
Related Categories
1 of 4
This Item | |||
|---|---|---|---|
| form powder | form - | form - | form - |
| assay ≥95.0% (TLC) | assay ≥95.0% (TLC) | assay ≥95.0% (HPLC) | assay ≥95.0% (TLC) |
| Quality Level 100 | Quality Level 100 | Quality Level 100 | Quality Level 100 |
| storage temp. −20°C | storage temp. −20°C | storage temp. −20°C | storage temp. −20°C |
Biochem/physiol Actions
Metabolite in monoterpenoid biosynthesis, substrate for monoterpene synthases.[1]
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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
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
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)
Charles Burke et al.
The Journal of biological chemistry, 277(5), 3141-3149 (2001-12-26)
Geranyl diphosphate synthase belongs to a subgroup of prenyltransferases, including farnesyl diphosphate synthase and geranylgeranyl diphosphate synthase, that catalyzes the specific formation, from C(5) units, of the respective C(10), C(15), and C(20) precursors of monoterpenes, sesquiterpenes, and diterpenes. Unlike farnesyl
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 76532-10MG | 04061832405186 |
| 76532-50MG | 04061832405193 |
Active Filters
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service

