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Merck
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671401

Sigma-Aldrich

N-Boc-N′-琥珀酰-4,7,10-三氧杂-1,13-十三烷二胺

95% (HPLC)

别名:

17-氧代-6,9,12-三氧杂-2,16-二氮杂二十烷二酸 1-(1,1-二甲基乙基)酯

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About This Item

经验公式（希尔记法）:
C19H36N2O8
CAS号:
250612-31-8
分子量:
420.50
MDL编号:
MFCD10566970
UNSPSC代码:
12352116
PubChem化学物质编号:
329760420
NACRES:
NA.22

质量水平

100

方案

95% (HPLC)

反应适用性

reagent type: cross-linking reagent

官能团

Fmoc
amine
carboxylic acid

储存温度

−20°C

SMILES字符串

O=C(CCC(O)=O)NCCCOCCOCCOCCCNC(OCC1C2=C(C=CC=C2)C3=C1C=CC=C3)=O

InChI

1S/C19H36N2O8/c1-19(2,3)29-18(25)21-9-5-11-27-13-15-28-14-12-26-10-4-8-20-16(22)6-7-17(23)24/h4-15H2,1-3H3,(H,20,22)(H,21,25)(H,23,24)

InChI key

RTHQDNQOODHVLK-UHFFFAOYSA-N

相关类别

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H302

危险分类

Acute Tox. 4 Oral

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCBZ8186
BCCM4305
BCCK9519
BCBW9547
BCBW9548

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Maria Davydova et al.
Journal of visualized experiments : JoVE, (145) (2019-03-26)
Maleimide-bearing bifunctional probes have been employed for decades for the site-selective modification of thiols in biomolecules, especially antibodies. Yet maleimide-based conjugates display limited stability in vivo because the succinimidyl thioether linkage can undergo a retro-Michael reaction. This, of course, can

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