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Merck
CN

471801

4-戊烯酐

98%

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线性分子式:
(H2C=CHCH2CH2CO)2O
化学文摘社编号:
分子量:
182.22
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
98%
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InChI

1S/C10H14O3/c1-3-5-7-9(11)13-10(12)8-6-4-2/h3-4H,1-2,5-8H2

SMILES string

C=CCCC(=O)OC(=O)CCC=C

InChI key

NEDHQDYBHYNBIF-UHFFFAOYSA-N

assay

98%

refractive index

n20/D 1.447 (lit.)

bp

78-81 °C/0.4 mmHg (lit.)

density

0.997 g/mL at 25 °C (lit.)

functional group

allyl, anhydride, ester

Quality Level

General description

4-戊烯酸酐是一种羧酸酐。

Application

4-戊烯酸酐可用于:
  • 葡萄糖官能化(共)聚合物的制备。
  • 作为单体用于交联聚酸酐的制备。
  • 用于制备具有侧链乙烯基或乙炔的聚合物。

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Marlène Rippe et al.
Biomaterials science, 7(7), 2850-2860 (2019-05-10)
Glycosaminoglycans (GAGs) are important components of the extracellular matrix that have attracted great interest for drug delivery and pharmaceutical applications due to their diverse biological functions. Among GAGs, heparosan (Hep), a biosynthetic precursor of heparin, has recently emerged as a
Katie L Poetz et al.
Biomacromolecules, 15(7), 2573-2582 (2014-05-23)
Several critical aspects of cross-linked polyanhydrides made using thiol-ene polymerization are reported, in particular the erosion, release, and solution properties, along with their cytotoxicity toward fibroblast cells. The monomers used to synthesize these polyanhydrides were 4-pentenoic anhydride and pentaerythritol tetrakis(3-mercaptopropionate).
Studies of the mechanism of the hypoglycemic action of 4-pentenoic acid.
Corredor C, et al.
Proceedings of the National Academy of Sciences of the USA, 58(6), 2299-2299 (1967)
Gaojian Chen et al.
Chemical communications (Cambridge, England), (10)(10), 1198-1200 (2009-02-26)
Homopolymer and block copolymer bearing carbohydrate side chain functionality were obtained by grafting glucothiose onto alkene functional scaffolds via a thiol-ene click reaction and the resulting copolymer was used to form thermo-responsive micelles as a potential drug carrier.
2-(Trimethylsilyl) ethyl Glycosides. Transformation into the Corresponding 1-O-Acyl Sugars.
Ellervik U and Magnusson G.
Acta Chemica Scandinavica, 47, 826-826 (1993)

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