Skip to Content
Merck
CN
All Photos(1)

Documents

Safety Information

W332607

Sigma-Aldrich

Acetone

≥99%, meets FCC analytical specifications

Synonym(s):

2-oxo propane, Dimethyl ketone, Propan-2-one, Pyroacetic acid

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
CH3COCH3
CAS Number:
67-64-1
Molecular Weight:
58.08
FEMA Number:
3326
Beilstein:
635680
EC Number:
200-662-2
Council of Europe no.:
737
MDL number:
MFCD00008765
UNSPSC Code:
12164502
PubChem Substance ID:
24901643
Flavis number:
7.050
NACRES:
NA.02

biological source

synthetic

Quality Level

400

grade

Halal

reg. compliance

FDA 21 CFR 173.210
FDA 21 CFR 175.105
FDA 21 CFR 175.320
FDA 21 CFR 176.180
FDA 21 CFR 176.300
meets analytical specifications of FCC

vapor density

2 (vs air)

vapor pressure

184 mmHg ( 20 °C)

Assay

≥99%

form

liquid

expl. lim.

13.2 %

color

clear colorless

refractive index

n20/D 1.359 (lit.)

pH

5-6 (20 °C, 395 g/L)

bp

56 °C/760 mmHg (lit.)

mp

−94 °C (lit.)

density

0.791 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

format

neat

Organoleptic

apple; ethereal

SMILES string

CC(C)=O

InChI

1S/C3H6O/c1-3(2)4/h1-2H3

InChI key

CSCPPACGZOOCGX-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Acetone′s luminesence intensity is dependent upon the solution components . The absorption of UV light by acetone, results in its photolysis and the production of radials .

Disclaimer

For R&D or non-EU Food use. Not for retail sale.

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Statements

H225,H319,H336

Precautionary Statements

P210 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

Target Organs

Central nervous system

Supplementary Hazards

EUH066

WGK

WGK 1

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品
易制毒化学品（3类）

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Oleksiy Krupin et al.
Optics express, 21(1), 698-709 (2013-02-08)
Straight long-range surface plasmon waveguides are demonstrated as biosensors for the detection of cells, proteins and changes in the bulk refractive index of solutions. The sensors consist of 5 μm wide 22 nm thick Au stripes embedded in polymer (CYTOP™)
Len Verbeke et al.
Hepatology (Baltimore, Md.), 59(6), 2286-2298 (2013-11-22)
The farnesoid X receptor (FXR) is a nuclear bile acid receptor involved in bile acid homeostasis, hepatic and intestinal inflammation, liver fibrosis, and cardiovascular disease. We studied the effect of short-term treatment with obeticholic acid (INT-747), a potent selective FXR
Wanqiang Sheng et al.
Cell research, 24(12), 1387-1402 (2014-11-22)
T helper (TH)-cell subsets, such as TH1 and TH17, mediate inflammation in both peripheral tissues and central nervous system. Here we show that STAT5 is required for T helper-cell pathogenicity in autoimmune neuroinflammation but not in experimental colitis. Although STAT5
Hugo Lövheim et al.
Alzheimer's & dementia : the journal of the Alzheimer's Association, 11(6), 593-599 (2014-07-22)
Previous studies have suggested a link between herpes simplex virus (HSV) type 1 and the development of Alzheimer's disease (AD). The present analysis included 3432 persons (53.9% women, mean age at inclusion 62.7 ± 14.4 years) with a mean follow-up
Juan A López-Ráez et al.
Plant science : an international journal of experimental plant biology, 230, 59-69 (2014-12-07)
Apocarotenoids are a class of compounds that play important roles in nature. In recent years, a prominent role for these compounds in arbuscular mycorrhizal (AM) symbiosis has been shown. They are derived from carotenoids by the action of the carotenoid
View All Related Papers

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