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Merck
모든 사진(5)

문서

A6283

Sigma-Aldrich

Acetic acid

glacial, ReagentPlus®, ≥99%

동의어(들):

Glacial acetic acid

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About This Item

Linear Formula:
CH3CO2H
CAS Number:
Molecular Weight:
60.05
Beilstein:
506007
EC Number:
MDL number:
UNSPSC 코드:
12352106
PubChem Substance ID:
NACRES:
NA.21

vapor density

2.07 (vs air)

Quality Level

제품 라인

ReagentPlus®

분석

≥99%

형태

liquid

autoignition temp.

800 °F

expl. lim.

16 %, 92 °F
4 %, 59 °F

refractive index

n20/D 1.371 (lit.)

pH

2.5 (20 °C, 50 g/L)

bp

117-118 °C (lit.)

mp

16.2 °C (lit.)

solubility

alcohol: miscible(lit.)
carbon disulfide: insoluble(lit.)
glycerol: miscible(lit.)
water: miscible(lit.)

density

1.04 g/mL at 25 °C (lit.)

저장 온도

room temp

SMILES string

[F2C(F2C)13F3C]C(O)=O

InChI

1S/C2H4O2/c1-2(3)4/h1H3,(H,3,4)

InChI key

QTBSBXVTEAMEQO-UHFFFAOYSA-N

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관련 카테고리

일반 설명

Acetic acid is an aliphatic organic acid. It is a hygroscopic, corrosive liquid with a vinegar-like odor. It can be synthesized by oxidizing acetaldehyde in the presence of manganese or cobalt salts. It is utilized for synthesizing acetic anhydride, cellulose acetate and acetic esters. Its impact on the degradation of historic paper has been analyzed.

애플리케이션

Acetic acid (AcOH) can be used as:      
  • A reaction solvent in many organic reactions such as bromination, hydrolysis, solvolysis, reductions, and hydrogenations.      
  • A reagent in the protonolysis of organometallic compounds.
  • An acetylating agent for the acetylation of electron-rich aromatic compounds.      
  • A catalyst to synthesize di(indolyl)methanes by the condensation reaction of indole and aromatic aldehydes.      
  • A solvent system to prepare 3,4-dihydropyrimidin-2(1H)-one derivative via Biginelli reaction of aromatic aldehydes, 1,3-dicarbonyl compounds, and urea in the presence of a boric acid catalyst.

Acetic acid can also be used in the following:     
  • Manganese(III) acetate/AcOH catalytic system is used in the conversion of alkenes to lactones.      
  • Iron salts/AcOH is used to oxidize 2-methylnaphthalene to 2-methyl-1-naphthol in the presence of H2O2.

특징 및 장점

  • Good stability towards many reagents     
  • Excellent solubility of organic compounds in this reagent

법적 정보

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

픽토그램

FlameCorrosion

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


시험 성적서(COA)

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문서 라이브러리 방문

이미 열람한 고객

Eagleson M.
Concise Encyclopedia Chemistry, 5-5 (1994)
Maize Kernels-Fixation in FAA, Embedding, Sectioning and Feulgen Staining.
Kladnik A.
Bio-protocol, 3(15), e835-e835 (2013)
Thermooxidative aging of polydicyclopentadiene in glassy state.
Richaud E, et al.
Polymer Degradation and Stability, 102, 95-104 (2014)
Acetic acid catalyzed carbon aerogels.
Brandt R, et al.
Journal of Porous Materials, 10(3), 171-178 (2003)
Effects of NO2 and acetic acid on the stability of historic paper.
Menart Eet al.
Cellulose, 21(5), 3701-3713 (2014)

프로토콜

Preparation of Plasmid DNA by Alkaline Lysis with SDS: Maxipreparation between Cold Spring Harbor Laboratory Press and our research team.

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