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제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
(CH3CO)2O
CAS 번호:
Molecular Weight:
102.09
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
203-564-8
MDL number:
Beilstein/REAXYS Number:
385737
Assay:
≥98.0%
Form:
liquid
제품 이름
Acetic anhydride, ACS reagent, ≥98.0%
grade
ACS reagent
Quality Level
vapor density
3.5 (vs air)
vapor pressure
10 mmHg ( 36 °C), 4 mmHg ( 20 °C)
assay
≥98.0%
form
liquid
autoignition temp.
629 °F
expl. lim.
10.3 %
impurities
MnO4- reducers, passes test
evapn. residue
≤0.003%
refractive index
n20/D 1.390 (lit.)
bp
138-140 °C (lit.)
mp
−73 °C (lit.)
solubility
H2O: slightly soluble
density
1.08 g/mL (lit.)
anion traces
chloride (Cl-): ≤5 ppm, phosphate (PO43-): ≤0.001%, sulfate (SO42-): ≤5 ppm
cation traces
Fe: ≤5 ppm, heavy metals: ≤2 ppm
functional group
anhydride, ester
SMILES string
CC(=O)OC(C)=O
InChI
1S/C4H6O3/c1-3(5)7-4(2)6/h1-2H3
InChI key
WFDIJRYMOXRFFG-UHFFFAOYSA-N
General description
Acetic anhydride is an organic solvent. On dissolution in water it undergoes solvolysis to afford acetic acid. It is widely employed for the acetylation of various alcohols. Wacher process (starting reagent + a ketene) and Knapsack process (starting reagent = acetaldehyde) have been reported for the industrial preparation of acetic anhydride.
Application
Acetic anhydride has been used as one of the reaction components in the preparation of:
- 2-acetylamino-5-aminobenzenesulfonic acid
- 3,3′-bis(sulfonato)-4,4′-bis(chloroacetamido)azobenzene (BSBCA)
- 10-acetoxy-9-nitro-octadecanoic acid, allyl ester
- 9-nitro-oleic acid
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
저장 등급
3 - Flammable liquids
wgk
WGK 1
flash_point_f
120.2 °F - closed cup
flash_point_c
49 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Acetylation of anisole by acetic anhydride over a HBEA zeolite-Origin of deactivation of the catalyst.
Rohan D, et al.
J. Catal., 177(2), 296-305 (1998)
Steven R Woodcock et al.
Free radical biology & medicine, 59, 14-26 (2012-12-04)
Nitrated fatty acids are the product of nitrogen dioxide reaction with unsaturated fatty acids. The discovery of peroxynitrite and peroxidase-induced nitration of biomolecules led to the initial reports of endogenous nitrated fatty acids. These species increase during ischemia/reperfusion, but concentrations
Darcy C Burns et al.
Nature protocols, 2(2), 251-258 (2007-04-05)
This protocol describes a procedure for the synthesis of 3,3'-bis(sulfonato)-4,4'-bis(chloroacetamido)azobenzene (BSBCA), a water-soluble, thiol-reactive, photo-switchable cross-linker. In addition, a protocol is outlined for installing the cross-linker in an intramolecular fashion onto proteins bearing two surface-exposed Cys residues. BSBCA is designed


