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G6772

Sigma-Aldrich

Geranyl pyrophosphate ammonium salt

≥95% (TLC), liquid

Synonyme(s) :

trans-3,7-Dimethyl-2,6-octadienyl pyrophosphate, GPP

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About This Item

Formule linéaire :
C10H20O7P2 · 3NH3
Numéro CAS:
763-10-0
Poids moléculaire :
365.30
Numéro MDL:
MFCD00189726
Code UNSPSC :
12352204
ID de substance PubChem :
24895272
Nomenclature NACRES :
NA.83

product name

Geranyl pyrophosphate ammonium salt, 1 mg/mL in methanol (:aqueous 10 mM NH4OH (7:3)), ≥95% (TLC)

Niveau de qualité

200

Pureté

≥95% (TLC)

Forme

liquid

Conditionnement

vial of 200 μg

Concentration

1 mg/mL in methanol (:aqueous 10 mM NH4OH (7:3))

Température de stockage

−20°C

Chaîne SMILES 

C\C(C)=C\CC\C(C)=C\COP(O)(=O)OP(O)(O)=O

InChI

1S/C10H20O7P2/c1-9(2)5-4-6-10(3)7-8-16-19(14,15)17-18(11,12)13/h5,7H,4,6,8H2,1-3H3,(H,14,15)(H2,11,12,13)/b10-7+

Clé InChI

GVVPGTZRZFNKDS-JXMROGBWSA-N

Catégories apparentées

Actions biochimiques/physiologiques

Intermediate in terpene biosynthesis

Pictogrammes

FlameSkull and crossbonesHealth hazard
GHS02,GHS06,GHS08

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Organes cibles

Eyes,Central nervous system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

68.0 °F - closed cup

Point d'éclair (°C)

20 °C - closed cup

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificats d'analyse (COA)

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Jacob Schewe et al.
Nature communications, 10(1), 1005-1005 (2019-03-03)
Global impact models represent process-level understanding of how natural and human systems may be affected by climate change. Their projections are used in integrated assessments of climate change. Here we test, for the first time, systematically across many important systems
Wenping Yuan et al.
Science advances, 5(8), eaax1396-eaax1396 (2019-08-28)
Atmospheric vapor pressure deficit (VPD) is a critical variable in determining plant photosynthesis. Synthesis of four global climate datasets reveals a sharp increase of VPD after the late 1990s. In response, the vegetation greening trend indicated by a satellite-derived vegetation
Iryna Janssen et al.
International journal of medical microbiology : IJMM, 306(8), 652-656 (2016-10-04)
Since data about Clostridium difficile infection in sub-Saharan Africa are scarce, we determined its epidemiology and risk factors in a cross-sectional study in Eikwe, a rural community in Ghana. We tested stool samples from 176 hospitalized patients with diarrhoea and
Sophie Twelves et al.
The Journal of allergy and clinical immunology, 143(3), 1021-1026 (2018-07-24)
The term pustular psoriasis indicates a group of severe skin disorders characterized by eruptions of neutrophil-filled pustules. The disease, which often manifests with concurrent psoriasis vulgaris, can have an acute systemic (generalized pustular psoriasis [GPP]) or chronic localized (palmoplantar pustulosis
Savitha Dhandapani et al.
BMC genomics, 18(1), 463-463 (2017-06-16)
Magnolia champaca, commonly known as champak is a well-known tree due to its highly fragrant flowers. Champak floral scent is attributed to a complex mix of volatile organic compounds (VOCs). These aromatic flowers are widely used in flavors and fragrances
Afficher tous les articles scientifiques apparentés

Articles

Cholesterol Biosynthesis

Cholesterol biosynthesis starts in the hepatic endoplasmic reticulum with acetyl-CoA, yielding 3-hydroxy-3-methylglutaryl-CoA via HMG-CoA synthase.

Cholesterol Biosynthesis

Cholesterol biosynthesis starts in the hepatic endoplasmic reticulum with acetyl-CoA, yielding 3-hydroxy-3-methylglutaryl-CoA via HMG-CoA synthase.

Cholesterol Biosynthesis

Cholesterol biosynthesis starts in the hepatic endoplasmic reticulum with acetyl-CoA, yielding 3-hydroxy-3-methylglutaryl-CoA via HMG-CoA synthase.

Cholesterol Biosynthesis

Cholesterol biosynthesis starts in the hepatic endoplasmic reticulum with acetyl-CoA, yielding 3-hydroxy-3-methylglutaryl-CoA via HMG-CoA synthase.

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