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234958

1,4-丁二醇二甲基丙烯酸酯

Name: 1,4-丁二醇二甲基丙烯酸酯
Brand: ALDRICH

95%, contains 200-300 ppm MEHQ as inhibitor

别名:

1,4-丁二醇二甲基丙烯酸酯, 丁二醇二甲基丙烯酸酯, 甲基丙烯酸四亚甲基酯

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关于此项目

线性分子式:

[H₂C=C(CH₃)CO₂CH₂CH₂-]₂

化学文摘社编号:

2082-81-7

分子量:

226.27

NACRES:

NA.23

PubChem Substance ID:

24854068

UNSPSC Code:

12162002

EC Number:

218-218-1

MDL number:

MFCD00008594

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属性

Quality Level

100

assay

95%

form

liquid

contains

200-300 ppm MEHQ as inhibitor

refractive index

n20/D 1.456 (lit.)

bp

132-134 °C/4 mmHg (lit.)

density

1.023 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CC(=C)C(=O)OCCCCOC(=O)C(C)=C

InChI

1S/C12H18O4/c1-9(2)11(13)15-7-5-6-8-16-12(14)10(3)4/h1,3,5-8H2,2,4H3

InChI key

XOJWAAUYNWGQAU-UHFFFAOYSA-N

说明

Application

1,4-BDDMA水泡状乳剂的配方及聚合：本研究的重点是1,4-丁二醇二甲基丙烯酸酯（1,4-BDDMA）在水乳液中的配方和聚合过程，展示了其在制造适用于各种工业应用的高性能聚合物泡沫方面的潜力（Dabrowski et al., 2020）。
甲基丙烯酸酯基聚合物泡沫具有可控制的连通性、孔隙形状、孔径大小和多分散性：该研究深入研究了使用1,4-BDDMA制造甲基丙烯酸酯基聚合物泡沫，强调了其在生产具有定制物理特性的材料方面的多功能性，这对生物医学和工业用途至关重要（Dabrowski et al., 2019）。
二氧化硅胶体晶体膜的双重复制：本文讨论了使用1,4-BDDMA复制二氧化硅胶体晶体薄膜，强调了其在为先进技术应用创建结构化材料方面的功效（Russell and Mallouk, 2017）。
基于聚丁二烯/多面体低聚硅氧烷的原位光交联纳米杂化弹性体：本研究研究了使用1,4-BDDMA的纳米杂化弹性体的开发，重点研究了其在医疗器械粘合剂和高性能聚合物合成中的应用（Mirmohammadi et al., 2016）。
甲基丙烯酸酯对牙髓细胞耗氧量和氧化还原状态的影响：研究强调了1,4-BDDMA的生物相容性和潜在的牙科应用，证明了它对人类牙髓细胞的影响，这对牙科复合材料至关重要（Nocca et al., 2014）。

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pictograms

GHS07

signalword

Warning

hcodes

H315,H317,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

存储类别

10 - Combustible liquids

wgk

WGK 1

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Effects of 1,4-butanediol dimethacrylate and urethane dimethacrylate on HL-60 cell metabolism.

Giuseppina Nocca et al.

European journal of oral sciences, 117(2), 175-181 (2009-03-27)

The polymerization of methacrylic monomers present in dental composite resins never reaches completion and therefore the leakage of residual monomers into the oral cavity and into biological fluids can cause local and systemic adverse effects. This work was carried out

Analysis of residual monomers in dendritic methacrylate copolymers and composites by HPLC and headspace-GC/MS.

Eeva K Viljanen et al.

Dental materials : official publication of the Academy of Dental Materials, 22(9), 845-851 (2005-12-29)

The aim of this study was to analyze the residual monomer content of photopolymerized dendritic methacrylate copolymers and particulate filler composites. Headspace-gas chromatography/mass spectrometry (HS-GC/MS) was compared with high performance liquid chromatography (HPLC). The resin mixtures consisted of a dendritic

Synthesis of esculentin-1 antibacterial peptide fragments on 1,4-butanediol dimethacrylate cross-linked polystyrene support.

M Roice et al.

Journal of protein chemistry, 20(1), 25-32 (2001-05-02)

Peptide segments corresponding to antibacterial esculentin-1 (1-15), (3344), (9-27), and their modified forms were synthesized on 1,4-butanediol dimethacrylate cross-linked polystyrene (PS-BDODMA) support. Hydroxymethyl and aminomethyl 2% PS-BDODMA supports were used for the synthesis. The HMPB linker was appended to the

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全球贸易项目编号

货号	GTIN
234958-100G	04061838784858
234958-500G	04061837404696