Eugenol natural, ≥98%, FG

Properties

Related Categories	Alphabetical Listings, Bioactive Small Molecules, Cell Biology, Certified Food Grade Products, Certified Natural Products, E, E-F, E-H, Flavors and Fragrances, Kosher Certified Products More...
grade	FG
	Kosher
	natural
reg. compliance	FDA 21 CFR (177.2800)
	FDA 21 CFR (184.1257)
	EU Regulation 1334/2008 & 178/2002
assay	≥98%
refractive index	n20/D 1.541(lit.)
bp	254 °C(lit.)
mp	−12-−10 °C(lit.)
density	1.067 g/mL at 25 °C(lit.)
Organoleptic	cinnamon; clove; spicy
allergen	no known allergens
Gene Information	human ... UGT1A4(54657)

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Description

Packaging

1 kg in glass bottle

1 sample in glass bottle

5, 10 kg in poly drum

Other Notes

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Price and Availability

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Related Papers

Structure-activity relationships of 1'S-1'-acetoxychavicol acetate for inhibitory effect on NO production in lipopolysaccharide-activated mouse peritoneal macrophages. Hisashi Matsuda et al Bioorg. Med. Chem. Lett. 15, 1949-53, (2005)

Documents

Certificate of Analysis

Certificate of Origin

Allergen Statement

Continuing Guarantee Statement

EU Natural Statement

FT-IR Raman

FT-NMR

Food Grade Statement

GMO Statement

Kosher Certificate (4 MB )

Pressure-Temperature Nomograph

Safety Information

Symbol	GHS07, GHS08
Signal word	Danger
Hazard statements	H302-H315-H317-H319-H334-H335
Precautionary statements	P261-P280-P305 + P351 + P338-P342 + P311
Personal Protective Equipment	Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Hazard Codes (Europe)	Xn
Risk Statements (Europe)	22-36/37/38-42/43
Safety Statements (Europe)	26-36
WGK Germany	3
RTECS	SJ4375000
Flash Point(F)	233.6 °F
Flash Point(C)	112 °C

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

Papers

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Structure-activity relationships of 1'S-1'-acetoxychavicol acetate for inhibitory effect on NO production in lipopolysaccharide-activated mouse peritoneal macrophages. Hisashi Matsuda et al Bioorg. Med. Chem. Lett. 15, 1949-53, (2005)

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Expanding the ChemGPS chemical space with natural products. Josefin Larsson et al J. Nat. Prod. 68, 985-91, (2005)

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CYP53A15 of Cochliobolus lunatus, a target for natural antifungal compounds. Barbara Podobnik et al J. Med. Chem. 51, 3480-6, (2008)

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Design and synthesis of eugenol derivatives, as potent 15-lipoxygenase inhibitors. Hamid Sadeghian et al Bioorg. Med. Chem. 16, 890-901, (2008)

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Phenolic glycosides from berries of Pimenta dioica. Hiroe Kikuzaki et al J. Nat. Prod. 71, 861-5, (2008)

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Design, synthesis and SAR studies of 4-allyoxyaniline amides as potent 15-lipoxygensae inhibitors. Seyed Mohammad Seyedi et al Bioorg. Med. Chem. 17, 1614-22, (2009)

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Design and synthesis of 4-methoxyphenylacetic acid esters as 15-lipoxygenase inhibitors and SAR comparative studies of them. Hamid Sadeghian et al Bioorg. Med. Chem. 17, 2327-35, (2009)

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Effect of essential oils, such as raspberry ketone and its derivatives, on antiandrogenic activity based on in vitro reporter gene assay. Yoshihisa Ogawa et al Bioorg. Med. Chem. Lett. 20, 2111-4, (2010)

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Merck 14,3898

Beil. 6,IV,6337

Arctander, 1369 / Corp MSDS 1 (1), 1670:D / FT-IR 1 (1), 1091:A / FT-IR 2 (2), 1868:B / FT-NMR 1 (2), 278:A / Fenaroli, 274 / IR-Spectra (2), 585:E / IR-Spectra (3), 656:B / NMR-Reference 2 (1), 896:D / RegBook 1 (1), 1283:E / RegBook 69 (1), 1283:E / Sax 6, 1402 / Sigma FT-IR 1 (2), 559:D / Structure Index 1, 195:D:8 / Vapor Phase 3, 1028:A