Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

W263605

Sigma-Aldrich

Linalyl acetate

≥97%, FCC, FG

Synonym(s):

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

Sign Into View Organizational & Contract Pricing

Select a Size

W263605-SAMPLE-K
$53.48
1 KG
$84.50

$53.48

List Price$56.30Save 5%
Web-Only Promotion

Available to ship onApril 24, 2025Details


Request a Bulk OrderRequest more information

Select a Size

Change View
W263605-SAMPLE-K
$53.48
1 KG
$84.50

About This Item

Linear Formula:
CH3CO2C(CH=CH2)(CH3)CH2CH2CH=C(CH3)2
CAS Number:
Molecular Weight:
196.29
FEMA Number:
2636
Beilstein/REAXYS Number:
1724500
EC Number:
Council of Europe no.:
203
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
9.013
NACRES:
NA.21
organoleptic:
green; woody; floral; sweet
grade:
FG
Kosher
biological source:
synthetic
agency:
meets purity specifications of JECFA
food allergen:
no known allergens

$53.48

List Price$56.30Save 5%
Web-Only Promotion

Available to ship onApril 24, 2025Details


Request a Bulk OrderRequest more information

biological source

synthetic

Quality Level

grade

FG
Kosher

agency

meets purity specifications of JECFA

reg. compliance

EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 117
FDA 21 CFR 182.60

vapor density

6.8 (vs air)

vapor pressure

0.1 mmHg ( 20 °C)

description

synthetic

assay

≥97%

refractive index

n20/D 1.453 (lit.)

bp

220 °C (lit.)

density

0.901 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

green; woody; floral; sweet

SMILES string

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

Inchi Key

UWKAYLJWKGQEPM-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Linalyl acetate is the main component of many plant essential oils[1] such as lavender oil.[2] It can be used as a flavoring agent[3] and fragrance ingredient.[4]

Pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

201.2 °F - closed cup

flash_point_c

94 °C - closed cup

ppe

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


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Dictionary of Food Compounds with CD-ROM: Additives, Flavors, and Ingredients, 573-573 (2012)
Krzysztof Cal
Planta medica, 72(4), 311-316 (2006-03-25)
The purpose of this study was to evaluate the in vitro cutaneous penetration of five terpenes--linalool, linalyl acetate, terpinen-4-ol, citronellol and alpha-pinene--applied in pure essential oils or in dermatological formulations (o/w emulsion, oily solution or hydrogel) containing 0.75 % w/w
Marina Soković et al.
Molecules (Basel, Switzerland), 15(11), 7532-7546 (2010-10-30)
The chemical composition and antibacterial activity of essential oils from 10 commonly consumed herbs: Citrus aurantium, C. limon, Lavandula angustifolia, Matricaria chamomilla, Mentha piperita, M. spicata, Ocimum basilicum, Origanum vulgare, Thymus vulgaris and Salvia officinalis have been determined. The antibacterial
Antonella Di Sotto et al.
Environmental and molecular mutagenesis, 52(1), 69-71 (2010-09-15)
The potential genotoxicity of lavender essential oil and its major components, linalool, and linalyl acetate, was evaluated in vitro by the micronucleus test on peripheral human lymphocytes. In the range of non-toxic concentrations (0.5-100 μg/ml), linalyl acetate increased the frequency
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

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service