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Merck
CN

106615

Sigma-Aldrich

2,2-双(羟甲基)丙酸

98%

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别名:
Bis-MPA, DMPA®, 二羟甲基丙酸
线性分子式:
(HOCH2)2C(CH3)COOH
CAS号:
分子量:
134.13
Beilstein:
1756385
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

蒸汽密度

<1 (vs air)

质量水平

检测方案

98%

形式

solid

mp

189-191 °C (lit.)

溶解性

H2O: soluble
acetone: slightly soluble
benzene: insoluble
methanol: soluble

SMILES字符串

CC(CO)(CO)C(O)=O

InChI

1S/C5H10O4/c1-5(2-6,3-7)4(8)9/h6-7H,2-3H2,1H3,(H,8,9)

InChI key

PTBDIHRZYDMNKB-UHFFFAOYSA-N

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应用

2,2-双(羟甲基)丙酸用于聚甲基硅氧烷(Si-PUD)改性聚氨酯分散体的合成和表征研究及其与粘土结合的纳米复合材料。2,2-双(羟甲基)丙酸基树枝状大分子在作为顺铂和多柔比星等强效抗癌药物的递送系统以及硼中子俘获疗法和光动力疗法的药剂方面具有很大的应用价值
2,2-双(羟甲基)丙酸通常用作AB2 单体,用于合成超支化(hb)聚合物和树枝状大分子。
以2,2-双(羟甲基)丙酸合成了具有48个羟基的第四代三分枝树枝状大分子
该酸简单衍生后就可通过“点击”叠氮-炔环加成反应来构建树枝状结构。

法律信息

DMPA is a registered trademark of GEO Specialty Chemicals, Inc.

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2

WGK

WGK 3

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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Elizabeth R Gillies et al.
Drug discovery today, 10(1), 35-43 (2005-01-29)
The unique properties of dendrimers, such as their high degree of branching, multivalency, globular architecture and well-defined molecular weight, make them promising new scaffolds for drug delivery. In the past decade, research has increased on the design and synthesis of
Synthesis and Characterization of Siloxane-Modified Polyurethane Dispersion/Clay Nanocomposites.
Noh HH, et al.
Advanced Materials Research, 415, 1196-1199 (2012)
Structure buildup in hyperbranched polymers from 2, 2-bis (hydroxymethyl) propionic acid.
Magnusson H, et al.
Macromolecules, 33(8), 3099-3104 (2000)
Double-stage convergent approach for the synthesis of functionalized dendritic aliphatic polyesters based on 2, 2-bis (hydroxymethyl) propionic acid.
Ihre H and Hult A.
Macromolecules, 31(13), 4061-4068 (1998)
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Biomaterials science, 7(6), 2288-2296 (2019-04-25)
Cationic aliphatic polycarbonates bearing primary ammonium side chains have been developed with relatively high molecular weights and controlled macromolecular architectures. These polycarbonates exhibit reasonable antimicrobial activity against Gram-negative and Gram-positive bacteria. The prepared homopolymers could be effective against Gram-negative bacteria

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