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695092

Sigma-Aldrich

Acetic acid

glacial, ACS reagent, ≥99.7%

Synonyma:

Glacial acetic acid

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About This Item

Lineární vzorec:
CH3CO2H
Číslo CAS:
64-19-7
Molekulová hmotnost:
60.05
Beilstein/REAXYS Number:
506007
EC Number:
200-580-7
MDL number:
MFCD00036152
UNSPSC Code:
12352106
PubChem Substance ID:
329761715
NACRES:
NA.21

grade

ACS reagent

Quality Level

200

vapor density

2.07 (vs air)

vapor pressure

11.4 mmHg ( 20 °C)

assay

≥99.7%

form

liquid

autoignition temp.

800 °F

expl. lim.

16 %, 92 °F
4 %, 59 °F

technique(s)

mass spectrometry (MS): suitable

impurities

Cr2O72- reducers, passes test
 MnO4- reducers, passes test
≤0.0004 meq/g Titr. base
≤0.01% acetic anhydride

evapn. residue

≤0.001%

color

APHA: ≤10

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.)

density

1.04 g/mL at 25 °C (lit.)

anion traces

chloride (Cl-): ≤1 ppm
sulfate (SO42-): ≤1 ppm

cation traces

Fe: ≤0.2 ppm
heavy metals: ≤0.5 ppm (by ICP)

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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General description

Acetic acid is an organic carboxylic acid. It is a pungent smelling hygroscopic liquid. Glacial acetic acid is the anhydrous acetic acid. It forms dimers linked by hydrogen bonds in solution and gaseous commonly referred as phases. It is weakly acidic in nature.

Application

Acetic acid is widely employed as solvent for various oxidation reactions. It may be used in the analysis of synthetic peptides by electron transfer dissociation (ETD) tandem mass spectrometry (MS/MS). It may be used in the preparation of peroxyacetic acid (disinfectant), via reaction with perhydrol (30% hydrogen peroxide).

Other Notes

4L and 4X4L are packaged in poly bottles

pictograms

FlameCorrosion
GHS02,GHS05

signalword

Danger

hcodes

H226,H314

Hazard Classifications

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

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

102.2 °F - closed cup

flash_point_c

39 °C - closed cup

Osvědčení o analýze (COA)

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John E P Syka et al.
Proceedings of the National Academy of Sciences of the United States of America, 101(26), 9528-9533 (2004-06-24)
Peptide sequence analysis using a combination of gas-phase ion/ion chemistry and tandem mass spectrometry (MS/MS) is demonstrated. Singly charged anthracene anions transfer an electron to multiply protonated peptides in a radio frequency quadrupole linear ion trap (QLT) and induce fragmentation
Eagleson M.
Concise Encyclopedia Chemistry, 5-5 (1994)
Isabelle Brunet et al.
The Journal of clinical investigation, 124(7), 3230-3240 (2014-06-18)
Autonomic sympathetic nerves innervate peripheral resistance arteries, thereby regulating vascular tone and controlling blood supply to organs. Despite the fundamental importance of blood flow control, how sympathetic arterial innervation develops remains largely unknown. Here, we identified the axon guidance cue
Katharine Trenholme et al.
Antimicrobial agents and chemotherapy, 58(7), 3666-3678 (2014-04-16)
Therapies to prevent transmission of malaria parasites to the mosquito vector are a vital part of the global malaria elimination agenda. Primaquine is currently the only drug with such activity; however, its use is limited by side effects. The development
Xianbao Deng et al.
The New phytologist, 201(4), 1469-1483 (2013-11-26)
• Chalcone synthase (CHS) is the key enzyme in the first committed step of the flavonoid biosynthetic pathway and catalyzes the stepwise condensation of 4-coumaroyl-CoA and malonyl-CoA to naringenin chalcone. In plants, CHS is often encoded by a small family
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