推荐产品
蒸汽密度
4.5 (vs air)
质量水平
蒸汽压
10 mmHg ( 57.7 °C)
方案
97%
自燃温度
545 °F
expl. lim.
11.9 %
折射率
n20/D 1.404 (lit.)
沸点
167 °C (lit.)
mp
−43 °C (lit.)
溶解性
H2O: decomposes (when in contact with water)
密度
1.015 g/mL at 25 °C (lit.)
SMILES字符串
CCC(=O)OC(=O)CC
InChI
1S/C6H10O3/c1-3-5(7)9-6(8)4-2/h3-4H2,1-2H3
InChI key
WYVAMUWZEOHJOQ-UHFFFAOYSA-N
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应用
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。
警示用语：
Danger
危险声明
危险分类
Eye Dam. 1 - Skin Corr. 1B
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 1
闪点(°F)
165.2 °F - closed cup
闪点(°C)
74 °C - closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
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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