523216
甲基丙烯酰氯
97%, contains monomethyl ether hydroquinone as stabilizer
别名:
α-甲基丙烯酰氯, 2-甲基-2-丙烯酰氯, 2-甲基丙烯酰氯, 2-甲基丙烯酸氯, 甲基丙烯酸氯
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关于此项目
线性分子式:
CH2=C(CH3)COCl
化学文摘社编号:
分子量:
104.53
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
213-058-9
Beilstein/REAXYS Number:
878175
MDL number:
Quality Level
assay
97%
contains
monomethyl ether hydroquinone as stabilizer
refractive index
n20/D 1.442 (lit.)
bp
95-96 °C (lit.)
density
1.07 g/mL at 25 °C (lit.)
storage temp.
−20°C
SMILES string
CC(=C)C(Cl)=O
InChI
1S/C4H5ClO/c1-3(2)4(5)6/h1H2,2H3
InChI key
VHRYZQNGTZXDNX-UHFFFAOYSA-N
General description
甲基丙烯酰氯是甲基丙烯酸的澄清至略带颜色的氯化酸。加入单甲醚对苯二酚作为稳定剂，以防止自动聚合。在金属盐存在下与二异丙醚的反应是严格的。
Application
甲基丙烯酰氯用于生产聚合物：
- 通过使甲基丙烯酰氯与外消旋的α-氨基-ε-己内酰胺反应制备单体2-甲基丙烯酰胺基 - 己内酰胺。
- 以甲基丙烯酰氯和 L-组氨酸为原料制备功能性单体。
- 以甲基丙烯酰氯与胺进行酰胺化反应，在常压等离子体辐射下接枝到聚醚砜 (PES) 膜上，合成了一系列酰胺单体。
- 甲基丙烯酰氯与 HEMA/NVP 微球表面的羟基发生反应，在微球表面引入可聚合的双键。
- 合成了带有 2、3 和 6 臂的星形聚（d,l-丙交酯）低聚物，与甲基丙烯酰氯进行末端官能化，并在乳酸乙酯存在下进行光交联，作为非反应性稀释剂。
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Danger
Hazard Classifications
Acute Tox. 1 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - Skin Sens. 1
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
55.0 °F - closed cup
flash_point_c
12.8 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
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Ferry P W Melchels et al.
Biomaterials, 30(23-24), 3801-3809 (2009-05-02)
Porous polylactide constructs were prepared by stereolithography, for the first time without the use of reactive diluents. Star-shaped poly(D,L-lactide) oligomers with 2, 3 and 6 arms were synthesised, end-functionalised with methacryloyl chloride and photo-crosslinked in the presence of ethyl lactate
Alexander Burkhart et al.
Beilstein journal of organic chemistry, 10, 1951-1958 (2014-09-24)
The monomer 2-methacrylamido-caprolactam (4) was synthesized from methacryloyl chloride (3) and racemic α-amino-ε-caprolactam (2). Copolymerization of 4 with N,N-dimethylacrylamide (5) was carried out by a free-radical mechanism using 2,2'-azobis(2-methylpropionitrile) (AIBN) as an initiator. The new copolymers show a lower critical
Müfrettin Murat Sarı et al.
Colloids and surfaces. B, Biointerfaces, 84(1), 140-147 (2011-01-29)
Affinity adsorption technique is increasingly used for protein purification, separation and other biochemical applications. Therapeutic molecules such as antibodies, cytokines, therapeutic DNA and plasma proteins must be purified before characterization and utilization. The aim of this study was to prepare
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 523216-1L | 04061837408328 |
| 523216-100ML | 04061837408311 |