Geraniol 98% | Sigma-Aldrich

Properties

Related Categories	Acyclic, Alkenes, Allium sativum (Garlic), Building Blocks, Cancer Research, Chemical Synthesis, Chemopreventive Agents, Citrus aurantium (Seville orange), Elettaria Cardamomum (Cardamom), Enzyme Inhibitors, Humulus lupulus (Hops), Hypericum perforatum (St John′s wort), Lavandula angustifolia (Lavendar tea), Metabolic Pathways, Metabolomics, Nutrition Research, Ocimum basilicum (Basil), Organic Building Blocks, Phytochemicals by Plant (Food/Spice/Herb), Steroid Metabolism, Terpenoid Metabolism, Terpenoids, Vaccinium myrtillus (Bilberry), Zingiber officinale (Ginger) More...
vapor density	5.31 (vs air)
vapor pressure	~0.2 mmHg ( 20 °C)
assay	98%
refractive index	n20/D 1.474(lit.)
bp	229-230 °C(lit.)
density	0.879 g/mL at 20 °C(lit.)

Description

Packaging

25, 100 g in glass bottle

Price and Availability

Suggested Laboratory Gloves

This substance has been tested against several types of hand protection for CE compliance. Click below to find the recommended gloves for handling this product.

for splash & immersion protection

Related Papers

Modifications of the chemical structure of terpenes in antiplasmodial and antifungal drug research. David Olagnier et al Bioorg. Med. Chem. Lett. 17, 6075-8, (2007)

Documents

Certificate of Analysis

Certificate of Origin

FT-IR Raman

FT-NMR

Pressure-Temperature Nomograph

Safety Information

Symbol	GHS05, GHS07
Signal word	Danger
Hazard statements	H315-H317-H318
Precautionary statements	P280-P305 + P351 + P338
Personal Protective Equipment	Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Hazard Codes (Europe)	Xi
Risk Statements (Europe)	36-41-43
Safety Statements (Europe)	26-36/37
WGK Germany	1
RTECS	RG5830000
Flash Point(F)	226.4 °F
Flash Point(C)	108 °C

Technical information & documentation associated with this product is available in the Safety & Documentation tab.

Papers

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Modifications of the chemical structure of terpenes in antiplasmodial and antifungal drug research. David Olagnier et al Bioorg. Med. Chem. Lett. 17, 6075-8, (2007)

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Synthesis of phosphatidylated-monoterpene alcohols catalyzed by phospholipase D and their antiproliferative effects on human cancer cells. Yukihiro Yamamoto et al Bioorg. Med. Chem. Lett. 18, 4044-6, (2008)

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Surfactants, aromatic and isoprenoid compounds, and fatty acid biosynthesis inhibitors suppress Staphylococcus aureus production of toxic shock syndrome toxin 1. Peter J McNamara et al Antimicrob. Agents Chemother. 53, 1898-906, (2009)

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Merck 14,4403

Beil. 1,IV,2277

Aldrich MSDS 1, 988:C / Arctander, 1426 / Corp MSDS 1 (1), 1767:B / FT-IR 2 (1), 213:A / FT-IR 1 (1), 148:D / FT-NMR 1 (1), 225:A / Fenaroli, 294 / IR-Spectra (2), 87:A / IR-Spectra (3), 90:F / NMR-Reference 2 (1), 135:A / RegBook 1 (1), 153:M / RegBook 26 (1), 153:M / Sigma FT-IR 1 (1), 1340:A / Structure Index 1, 19:B:5 / Vapor Phase 3, 219:B