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Merck

12436

Sigma-Aldrich

Neryl pyrophosphate lithium salt

≥95.0% (TLC)

Sinónimos:

(Z)-3,7-Dimethyl-2,6-octadien-1-yl pyrophosphate lithium salt, Neryl diphosphate lithium salt

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About This Item

Fórmula empírica (notación de Hill):
C10H20O7P2 · xLi+
Número de CAS:
Peso molecular:
314.21 (free acid basis)
UNSPSC Code:
12352107
NACRES:
NA.25

Quality Level

assay

≥95.0% (TLC)

storage temp.

−20°C

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.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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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
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
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
R Croteau et al.
The Journal of biological chemistry, 264(26), 15309-15315 (1989-09-15)
(+)-Pinene cyclase from sage (Salvia officinalis) catalyzes the isomerization and cyclization of geranyl pyrophosphate to (+)-alpha-pinene and (+)-camphene, and to lesser amounts of (+)-limonene, myrcene, and terpinolene, whereas (-)-pinene cyclase from this tissue catalyzes the conversion of the acyclic precursor
Old substrates for new enzymes of terpenoid biosynthesis.
Jörg Bohlmann et al.
Proceedings of the National Academy of Sciences of the United States of America, 106(26), 10402-10403 (2009-06-26)

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