lauric acid n-hydroxy-succinimide ester

Names

[ Name ]:
lauric acid n-hydroxy-succinimide ester

[Synonym ]:
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

Biological Activity

[Description]:

(2,5-Dioxopyrrolidin-1-yl) dodecanoate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Chemical & Physical Properties

[ Density]:
1.07g/cm3

[ Boiling Point ]:
392.3ºC at 760mmHg

[ Molecular Formula ]:
C₁₆H₂₇NO₄

[ Molecular Weight ]:
297.39000

[ Flash Point ]:
191.1ºC

[ Exact Mass ]:
297.19400

[ PSA ]:
63.68000

[ LogP ]:
3.45240

[ Vapour Pressure ]:
2.31E-06mmHg at 25°C

[ Index of Refraction ]:
1.489

[ Storage condition ]:
−20°C

MSDS

Click to get detail MSDS

Safety Information

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2925190090

Synthetic Route

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Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2925190090

[ 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%

Articles

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)