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2,5-二氧代吡咯烷-1-基十二酸酯

2,5-二氧代吡咯烷-1-基十二酸酯用途

(2,5-二氧吡咯烷-1-基)十二烷酸酯是一种生物化学试剂,可作为生物材料或有机化合物用于生命科学相关研究。

2,5-二氧代吡咯烷-1-基十二酸酯名称

[ CAS 号 ]:
14565-47-0

[ 中文名 ]:
2,6-二甲基吡啶

[ 英文名 ]:
lauric acid n-hydroxy-succinimide ester

[英文别名 ]:

2,5-dioxopyrrolidin-1-yl dodecanoate
dodecanoic acid 2,5-dioxo-pyrrolidin-1-yl
Lauric acid N-hydroxysuccinimide ester
dodecanoic N-hydroxyl-succinimide ester
Succinimidyl laurate
2,5-dioxotetrahydro-1H-1-pyrrolyl laurate
dodecanoic acid 2,5-dioxopyrrolidin-1-yl ester
dodecanoic acid N-hydroxysuccinimide ester

2,5-二氧代吡咯烷-1-基十二酸酯生物活性

[ 描述 ]:

(2,5-二氧吡咯烷-1-基)十二烷酸酯是一种生物化学试剂,可作为生物材料或有机化合物用于生命科学相关研究。

[ 相关类别 ]:

研究领域 >> 其他

2,5-二氧代吡咯烷-1-基十二酸酯物理化学性质

[ 密度 ]:
1.07g/cm3

[ 沸点 ]:
392.3ºC at 760mmHg

[ 分子式 ]:
C₁₆H₂₇NO₄

[ 分子量 ]:
297.39000

[ 闪点 ]:
191.1ºC

[ 精确质量 ]:
297.19400

[ PSA ]:
63.68000

[ LogP ]:
3.45240

[ 蒸汽压 ]:
2.31E-06mmHg at 25°C

[ 折射率 ]:
1.489

[ 储存条件 ]:
−20°C

2,5-二氧代吡咯烷-1-基十二酸酯MSDS

2,5-二氧代吡咯烷-1-基十二酸酯安全信息

[ 危害码 (欧洲) ]:
Xi

[ 危险品运输编码 ]:
NONH for all modes of transport

[ WGK德国 ]:
3

[ 海关编码 ]:
2925190090

2,5-二氧代吡咯烷-1-基十二酸酯合成路线

2,5-二氧代吡咯烷-1-基十二酸酯上下游产品

2,5-二氧代吡咯烷-1-基十二酸酯上游产品

2,5-二氧代吡咯烷-1-基十二酸酯下游产品

2,5-二氧代吡咯烷-1-基十二酸酯海关

[ 海关编码 ]: 2925190090

[ 中文概述 ]:
2925190090 其他酰亚胺及其衍生物盐. 增值税率:17.0% 退税率:9.0% 监管条件:无最惠国关税:6.5% 普通关税:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途

[ Summary ]:
2925190090 other imides and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

2,5-二氧代吡咯烷-1-基十二酸酯文献

Water-soluble fatty acid derivatives as acylating agents for reversible lipidization of polypeptides.

FEBS Lett. 371 , 283-286, (1995)

A novel method allowing the conjugation of a fatty acid to a peptide or protein in aqueous buffer is described in this paper. L-Cysteinyl 2-pyridyl disulfide (CPD) (III), which was obtained by reactin...

Use of esters of N-hydroxysuccinimide in the synthesis of N-acylamino acids.

J. Lipid Res. 8 , 142-145, (1967)

Several crystalline N-hydroxysuccinimide esters of short- and long-chain fatty acids have been synthesized. These compounds react with free amino acids to form preferentially N-acylamino acids. The re...

Lipidization of human interferon-α: a new approach toward improving the delivery of protein drugs. Yuan L, Wang J, Shen WC.

J. Controlled Release 129 , 11-17, (2008)

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