Skip to Content
Merck
CN

00561

Acetone

≥99.5% (GC)

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
CH3COCH3
CAS Number:
Molecular Weight:
58.08
UNSPSC Code:
12352200
PubChem Substance ID:
eCl@ss:
39021201
EC Number:
200-662-2
Beilstein/REAXYS Number:
635680
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

CSCPPACGZOOCGX-UHFFFAOYSA-N

InChI

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

SMILES string

CC(C)=O

vapor pressure

184 mmHg ( 20 °C)

assay

≥99.5% (GC)

expl. lim.

13.2 %

color

clear colorless

mp

−94 °C (lit.)

density

0.791 g/mL at 25 °C (lit.)

λ

1 cm path, H2O reference

UV absorption

λ: 335 nm Amax: ≤0.30, λ: 340 nm Amax: ≤0.08, λ: 350 nm Amax: ≤0.003

suitability

in accordance for luminescence, suitable for luminescence

Looking for similar products? Visit Product Comparison Guide

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 .

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

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

target_organs

Central nervous system

supp_hazards

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

1.4 °F - closed cup

flash_point_c

-17.0 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support

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

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