W246719

Eugenol

natural, ≥98%, FG

• Sinónimos: 2-Methoxy-4-(2-propenyl)phenol, 4-Allyl-2-methoxyphenol, 4-Allylguaiacol
• Fórmula lineal: 4-(H₂C=CHCH₂)C₆H₃-2-(OCH₃)OH
• Número de CAS: 97-53-0
• Peso molecular: 164.20
• FEMA Number: 2467
• Beilstein/REAXYS Number: 1366759
• EC Number: 202-589-1
• Council of Europe no.: 171
• MDL number: MFCD00008654
• UNSPSC Code: 12164502
• PubChem Substance ID: 24901115
• Flavis number: 4.003
• NACRES: NA.21

Propiedades

• grade: FG; Fragrance grade; Halal; Kosher; natural
• Quality Level: 400
• agency: follows IFRA guidelines; meets purity specifications of JECFA
• reg. compliance: EU Regulation 1223/2009; EU Regulation 1334/2008 & 178/2002; FDA 21 CFR 117
• assay: ≥98%
• form: liquid
• composition: contains IFRA and EU 1223/2009 restricted Eugenol
• greener alternative product characteristics: Less Hazardous Chemical Syntheses; Use of Renewable Feedstocks; Learn more about the Principles of Green Chemistry.
• 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.)
• application(s): flavors and fragrances
• documentation: see Safety & Documentation for available documents
• food allergen: no known allergens
• fragrance allergen: eugenol
• greener alternative category: Aligned
• organoleptic: clove; woody; spicy; sweet
• SMILES string: COc1cc(CC=C)ccc1O
• InChI: 1S/C10H12O2/c1-3-4-8-5-6-9(11)10(7-8)12-2/h3,5-7,11H,1,4H2,2H3
• InChI key: RRAFCDWBNXTKKO-UHFFFAOYSA-N
• Gene Information: human ... UGT1A4(54657)

Descripción

General description

Eugenol is one of the key volatile constituents of cinnamon and clove oils.

We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product is a Biobased products, showing key improvements in Green Chemistry Principles “Less Hazardous Chemical Syntheses” and “Use of Renewable Feedstock”.

Application

• Methoxyeugenol Protects Against Lung Inflammation and Suppresses Neutrophil Extracellular Trap Formation in an LPS-Induced Acute Lung Injury Model.: This research highlights the protective effects of methoxyeugenol against lung inflammation and its potential to suppress neutrophil extracellular trap formation, indicating its therapeutic potential in inflammatory conditions (Antunes et al., 2022) (Antunes et al., 2022).


• Methoxyeugenol regulates the p53/p21 pathway and suppresses human endometrial cancer cell proliferation.: This research uncovers the ability of methoxyeugenol to regulate the p53/p21 pathway and inhibit the proliferation of human endometrial cancer cells, indicating its potential as an anticancer agent (Costa et al., 2021) (Costa et al., 2021).

Información de seguridad

• pictograms: GHS07
• signalword: Warning
• hcodes: H317,H319
• pcodes: P261 - P264 - P272 - P280 - P302 + P352 - P305 + P351 + P338
• Hazard Classifications: Eye Irrit. 2 - Skin Sens. 1
• Storage Class: 10 - Combustible liquids
• wgk_germany: WGK 1
• flash_point_f: 255.2 °F - closed cup
• flash_point_c: 124 °C - closed cup
• ppe: Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter