P51478
丙酸酐
97%
别名:
初油酸酐
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关于此项目
线性分子式:
(CH3CH2CO)2O
化学文摘社编号:
分子量:
130.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-638-2
Beilstein/REAXYS Number:
507066
MDL number:
Assay:
97%
InChI key
WYVAMUWZEOHJOQ-UHFFFAOYSA-N
InChI
1S/C6H10O3/c1-3-5(7)9-6(8)4-2/h3-4H2,1-2H3
SMILES string
CCC(=O)OC(=O)CC
vapor density
4.5 (vs air)
vapor pressure
10 mmHg ( 57.7 °C)
assay
97%
autoignition temp.
545 °F
expl. lim.
11.9 %
Quality Level
bp
167 °C (lit.)
mp
−43 °C (lit.)
solubility
H2O: decomposes (when in contact with water)
density
1.015 g/mL at 25 °C (lit.)
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Application
丙酐可作为酰化剂用于脂肪酶催化的醇类酯化反应。近年来的研究表明，丙酸酐改性木屑制备的刨花板具有较高的尺寸稳定性。
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
165.2 °F - closed cup
flash_point_c
74 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Dimensional stabilisation and strength of particleboard by chemical modification with propionic anhydride.
Papadopoulos AN & Gkaraveli A
European Journal of Wood and Wood Products, 61(2), 142-144 (2003)
Anhydrides as acylating agents in lipase-catalyzed stereoselective esterification of racemic alcohols.
Bianchi D, et al.
The Journal of Organic Chemistry, 53(23), 5531-5534 (1988)
Robert Meatherall et al.
Journal of analytical toxicology, 33(8), 525-531 (2009-10-31)
Azide in human blood and plasma samples was derivatized with propionic anhydride in a headspace vial without prior sample preparation. The reaction proceeds quickly at room temperature to form propionyl azide. A portion of the headspace was assayed by gas
Surendra Nimesh et al.
International journal of pharmaceutics, 337(1-2), 265-274 (2007-01-27)
Polyethylenimine (750 kDa) has been derivatized to influence the proton sponge mechanism and hydrophobic-hydrophilic balance. The polymer was acylated using acid anhydrides of varying carbon chain length, followed by cross-linking with PEG-bis-P to form compact nanoparticles. The chemical linkages in
Haim Tsubery et al.
The Journal of biological chemistry, 279(37), 38118-38124 (2004-06-11)
Polyethylene glycol (PEG)-conjugated therapeutic peptides/proteins have been shown to exhibit clinical properties superior to those of their corresponding unmodified parent molecules. However, the desirable pharmacological features gained by protein PEGylation become irrelevant if conjugates are inactivated or cannot reach their
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