12436
Neryl pyrophosphate lithium salt
≥95.0% (TLC)
Synonym(s):
(Z)-3,7-Dimethyl-2,6-octadien-1-yl pyrophosphate lithium salt, Neryl diphosphate lithium salt
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
| Pack Size | SKU | Availability | Price |
|---|
About This Item
Empirical Formula (Hill Notation):
C10H20O7P2 · xLi+
CAS Number:
Molecular Weight:
314.21 (free acid basis)
MDL number:
NACRES:
NA.25
UNSPSC Code:
12352107
Assay:
≥95.0% (TLC)
Quality level:
Pricing and availability is not currently available.
Application
Neryl pyrophosphate, the cis isomer of geranyl pyrophosphate, may be used to characterize and study the kinetics of enzymes such as 1,8-cineole synthase, farnesyl pyrophosphate synthase, pinene cyclase and geranyl pyrophosphate:sabinene hydrate cyclase.
Biochem/physiol Actions
Metabolite, substrate for monoterpene synthase.[1]
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
1 of 1
This Item | |||
|---|---|---|---|
| assay ≥95.0% (TLC) | assay ≥95.0% (TLC) | assay ≥95.0% (TLC) | 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 |
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
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.
D R Light et al.
The Journal of biological chemistry, 264(31), 18598-18607 (1989-11-05)
A prenyltransferase purified from the commercial rubber tree, Hevea brasiliensis, that elongates existing cis-polyisoprene rubber molecules also catalyzes the formation of all trans-farnesyl pyrophosphate (t,t-FPP) from dimethylallyl pyrophosphate (DMAPP) and isopentenyl pyrophosphate (IPP). In assays of the latter activity trans-geranyl
T W Hallahan et al.
Archives of biochemistry and biophysics, 264(2), 618-631 (1988-08-01)
A soluble enzyme preparation from the leaves of sweet marjoram (Majorana hortensis Moench) catalyzes the divalent cation-dependent cyclization of [1-3H]geranyl pyrophosphate to the bicyclic monoterpene alcohols (+)-[6-3H]cis- and (+)-[6-3H]-transsabinene hydrate, providing labeling patterns consistent with current mechanistic considerations. No free
R Croteau et al.
Archives of biochemistry and biophysics, 309(1), 184-192 (1994-02-15)
Geranyl pyrophosphate: 1,8-cineole cyclase (cineole synthase) catalyzes the conversion of geranyl pyrophosphate to the symmetrical monoterpene ether 1,8-cineole (1,3,3-trimethyl-2-oxabicyclo[2.2.2]octane) by a process thought to involve the initial isomerization of the substrate to the tertiary allylic isomer, linalyl pyrophosphate, and cyclization