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Merck
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文件

155721

Sigma-Aldrich

甲基丙烯酸

contains 250 ppm MEHQ as inhibitor, 99%

别名:

2-甲基丙烯酸, 异丁烯酸

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About This Item

线性分子式:
H2C=C(CH3)COOH
CAS号:
79-41-4
分子量:
86.09
Beilstein:
1719937
EC號碼:
201-204-4
MDL號碼:
MFCD00002651
分類程式碼代碼:
12162002
PubChem物質ID:
24849561
NACRES:
NA.23

蒸汽密度

>3 (vs air)

品質等級

200

蒸汽壓力

1 mmHg ( 20 °C)

化驗

99%

形狀

liquid

自燃溫度

752 °F

包含

250 ppm MEHQ as inhibitor

折射率

n20/D 1.431 (lit.)

pH值

2.0-2.2 (20 °C, 100 g/L)

bp

163 °C (lit.)

mp

12-16 °C (lit.)

密度

1.015 g/mL at 25 °C (lit.)

SMILES 字串

C=C(C)C(O)=O

InChI

1S/C4H6O2/c1-3(2)4(5)6/h1H2,2H3,(H,5,6)

InChI 密鑰

CERQOIWHTDAKMF-UHFFFAOYSA-N

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相关类别

一般說明

甲基丙烯酸（MAA）是一种有机化合物，无色，粘性液体。它是一种单功能甲基丙烯醛单体。它在温水中可溶解，可以和大多数有机溶剂混合。MAA可用作对应酯化产物的起始物质；尤其是甲基丙烯酸甲酯与聚甲基丙烯酸甲酯（PMMA）。

應用

MAA可用于合成聚（甲基丙烯酸）-g-聚(ε己内酯）共聚物，和PMMA以及甲基丙烯酸羟乙酯（HEMA）-MAA凝胶聚合共混合。

象形圖

Skull and crossbonesCorrosion
GHS06,GHS05

訊號詞

Danger

危險分類

Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1A - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

水污染物質分類（WGK）

WGK 1

閃點（°F）

152.6 °F - closed cup

閃點（°C）

67 °C - closed cup

個人防護裝備

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

分析证书(COA)

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1 of 2

甲基丙烯酸甲酯 European Pharmacopoeia (EP) Reference Standard

Y0001488

甲基丙烯酸甲酯

2-羟基乙基甲基丙烯酸酯 contains ≤250 ppm monomethyl ether hydroquinone as inhibitor, 97%

Sigma-Aldrich

128635

2-羟基乙基甲基丙烯酸酯

Reversible Addition Fragmentation Chain Transfer
(RAFT) Polymerization
Moad G, et al.
Material Matters, 5(1) (2010)
Synthesis of graft copolymers of poly(methacrylic acid)-g-poly(?-caprolactone) by coupling ROP and RAFT polymerizations
Kiehl J, et al.
Polymer, 53(3), 694-700 (2012)
Thomas J Dursch et al.
Biomaterials, 35(2), 620-629 (2013-10-24)
Two-photon confocal microscopy and back extraction with UV/Vis-absorption spectrophotometry quantify equilibrium partition coefficients, k, for six prototypical drugs in five soft-contact-lens-material hydrogels over a range of water contents from 40 to 92%. Partition coefficients were obtained for acetazolamide, caffeine, hydrocortisone
Josué A Torres-Ávalos et al.
Polymers, 13(4) (2021-03-07)
Design of a smart drug delivery system is a topic of current interest. Under this perspective, polymer nanocomposites (PNs) of butyl acrylate (BA), methacrylic acid (MAA), and functionalized carbon nanotubes (CNTsf) were synthesized by in situ emulsion polymerization (IEP). Carbon
Riteshkumar J Patel et al.
Journal of biomedical materials research. Part A, 100(8), 2054-2062 (2012-05-15)
Exudate analysis indicated that both hydroxamated methacrylic acid-based (HX-MAA) and methacrylic acid-based (MAA) beads without hydroxamation, implanted in an air pouch with gelatin discs, elicited similar biological responses, with both resulting in high cell counts and chemokine (MCP3) levels, relative
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