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Merck

320110

Acetone

ACS reagent, ≥99.5%

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About This Item

Linear Formula:
CH3COCH3
CAS Number:
Molecular Weight:
58.08
UNSPSC Code:
12352115
NACRES:
NA.21
PubChem Substance ID:
EC Number:
200-662-2
Beilstein/REAXYS Number:
635680
MDL number:
grade:
ACS reagent
assay:
≥99.5%
bp:
56 °C/760 mmHg (lit.)
vapor pressure:
184 mmHg ( 20 °C)

Product Name

Acetone, ACS reagent, ≥99.5%

InChI key

CSCPPACGZOOCGX-UHFFFAOYSA-N

InChI

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

SMILES string

CC(C)=O

grade

ACS reagent

agency

suitable for EPA 1613

vapor density

2 (vs air)

vapor pressure

184 mmHg ( 20 °C)

assay

≥99.5%

form

liquid

expl. lim.

13.2 %

dilution

(for analytical testing)

impurities

≤0.0003 meq/g Titr. acid
≤0.0006 meq/g Titr. base
≤0.002% aldehyde as formaldehyde
≤0.05% isopropanol
≤0.05% methanol
≤0.5% water

evapn. residue

≤0.001%

color

APHA: ≤10

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.)

format

neat

Quality Level

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Application

  • Used as solvent and/or building block in organic syntheses, such as SN2 reactions and Jones oxidation
  • Mobile phase in Thin layer chromatography (TLC)
  • Used as solvent in chemical molecules delivery systems in pharmaceutical and cosmetic industries
  • Cleaning proposes
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 .

Features and Benefits

ACS solvents meet or exceed the high standards of the American Chemical Society (ACS) ,with test specifications that are specialized to every compound. According to the American Chemical Society, ACS reagent grade implies that it is a substance of sufficient purity to be used in most chemical analyses or reactions

General description

Acetone is a polar, aprotic organic solvent. It is a colorless and highly volatile liquid. It is commonly used in organic syntheses as solvent and/or building block, in pharmaceutical and personal care industries. This grade meets ACS requirements, making it ideal for a wide range of analytical applications.
Our premium ACS solvents are ideal for routine chemical synthesis, drying, purification, and critical labware cleaning. They meet or exceed the rigorous standards of the American Chemical Society (ACS), ensuring high-quality results for your research needs.

Premium ACS Solvents: Our solvents meet or exceed the stringent standards set by the American Chemical Society, ensuring high quality and reliability for your laboratory applications.

Replicable and Publishable Results: Designed for consistency, our solvents deliver results that can be reliably reproduced, making them ideal for research that requires publication.

Versatile Applications: Suitable for routine chemical synthesis, drying, purification, and critical labware cleaning, our solvents cater to a wide range of research needs in the laboratory.

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


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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
Anna Hultberg et al.
PloS one, 6(4), e17665-e17665 (2011-04-13)
For efficient prevention of viral infections and cross protection, simultaneous targeting of multiple viral epitopes is a powerful strategy. Llama heavy chain antibody fragments (VHH) against the trimeric envelope proteins of Respiratory Syncytial Virus (Fusion protein), Rabies virus (Glycoprotein) and
Sinisa Bjelic et al.
Journal of molecular biology, 426(1), 256-271 (2013-10-29)
Designed retroaldolases have utilized a nucleophilic lysine to promote carbon-carbon bond cleavage of β-hydroxy-ketones via a covalent Schiff base intermediate. Previous computational designs have incorporated a water molecule to facilitate formation and breakdown of the carbinolamine intermediate to give the

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