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Documentos Principais

W263613

Sigma-Aldrich

Linalyl acetate

greener alternative

natural, ≥96%, FG

Sinônimo(s):

3,7-Dimethyl-1,6-octadien-3-yl acetate, Bergamol

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About This Item

Fórmula linear:
CH3CO2C(CH=CH2)(CH3)CH2CH2CH=C(CH3)2
Número CAS:
Peso molecular:
196.29
Número FEMA:
2636
Beilstein:
1724500
Número CE:
Conselho da Europa nº:
203
Número MDL:
Código UNSPSC:
12164502
ID de substância PubChem:
Número de Flavis:
9.013
NACRES:
NA.21

fonte biológica

botanical

Nível de qualidade

grau

FG
Halal
Kosher
natural

conformidade reg.

EU Regulation 1334/2008 & 872/2012
FDA 21 CFR 117

densidade de vapor

6.8 (vs air)

pressão de vapor

0.1 mmHg ( 20 °C)

Ensaio

≥96%

características do produto alternativo mais ecológico

Less Hazardous Chemical Syntheses
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

índice de refração

n20/D 1.453 (lit.)

p.e.

220 °C (lit.)

densidade

0.901 g/mL at 25 °C (lit.)

aplicação(ões)

flavors and fragrances

Documentação

see Safety & Documentation for available documents

alérgeno alimentar

no known allergens

categoria alternativa mais ecológica

Organoléptico

green; woody; floral; sweet

cadeia de caracteres SMILES

C\C(C)=C\CCC(C)(OC(C)=O)C=C

InChI

1S/C12H20O2/c1-6-12(5,14-11(4)13)9-7-8-10(2)3/h6,8H,1,7,9H2,2-5H3

chave InChI

UWKAYLJWKGQEPM-UHFFFAOYSA-N

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Descrição geral

Linalyl acetate is a monoterpene ester mainly found in lavandula essential oil. It is used as a flavoring agent in food industries, as well as a preservative additive in cosmetics and fragrances such as soaps, colognes, perfumes, and skin lotions.
We are committed to bringing you greener alternative products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product is Biobased and thus aligns with "Less Hazardous Chemical Syntheses" and "Use of Renewable Feedstocks".

Aplicação


  • Evaluation and estimation of diuretic activity of the linalyl acetate in the rats.: Focuses on the pharmacological effects of linalyl acetate, testing its diuretic activity in rats, which could lead to new therapeutic applications in medicine (Rafique et al., 2024).

  • Characterization of bergamot essential oil: chemical, microbiological and colloidal aspects.: Investigates the components of bergamot essential oil, including linalyl acetate, assessing its chemical properties and potential microbiological uses, supporting its diverse applications in cosmetics and therapeutics (Cordeiro et al., 2024).


Pictogramas

Exclamation mark

Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1B

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

201.2 °F - closed cup

Ponto de fulgor (°C)

94 °C - closed cup

Equipamento de proteção individual

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


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Linalool analytical standard

Supelco

51782

Linalool

(−)-Linalool ≥95.0% (sum of enantiomers, GC)

Sigma-Aldrich

62139

(−)-Linalool

1,8-Cineole primary reference standard

Supelco

00020590

1,8-Cineole

Dictionary of Food Compounds with CD-ROM: Additives, Flavors, and Ingredients, 573-573 (2012)
Domenico Trombetta et al.
Antimicrobial agents and chemotherapy, 49(6), 2474-2478 (2005-05-27)
In the present paper, we report the antimicrobial efficacy of three monoterpenes [linalyl acetate, (+)menthol, and thymol] against the gram-positive bacterium Staphylococcus aureus and the gram-negative bacterium Escherichia coli. For a better understanding of their mechanisms of action, the capability
Wafica S Itani et al.
Cancer biology & therapy, 7(11), 1765-1773 (2008-09-13)
Lebanese sage essential oil possesses antitumor properties, however, the bioactive components and antitumor mechanisms are not known. Here we show that combining the three sage bioactive compounds, Linalyl acetate (Ly), Terpeniol (Te) and Camphor (Ca), caused synergistic inhibition of the
Maria Sköld et al.
Contact dermatitis, 58(1), 9-14 (2007-12-25)
Fragrances are among the most common causes of allergic contact dermatitis. We have in previous studies shown that linalool, present in lavender oil, autoxidizes on air exposure, forming allergenic oxidation products. Oxidized linalool was found to be a frequent cause
Olga Larkov et al.
Phytochemistry, 69(14), 2565-2571 (2008-10-07)
Selected plants within the Origanum, Mentha and Salvia genera, that contain significant amounts of chiral volatile alcohols and their related acetates, exhibit remarkable enantioselectivity of alcohol acetyl transferase (AAT) activity and particularly can discriminate between linalool enantiomers. Origanum dayi AAT

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