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Merck
CN

671401

N-Boc-N′-succinyl-4,7,10-trioxa-1,13-tridecanediamine

95% (HPLC)

Synonym(s):

17-Oxo-6,9,12-trioxa-2,16-diazaeicosanedioic acid 1-(1,1-dimethylethyl)ester

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About This Item

Empirical Formula (Hill Notation):
C19H36N2O8
CAS Number:
250612-31-8
Molecular Weight:
420.50
NACRES:
NA.22
PubChem Substance ID:
329760420
UNSPSC Code:
12352116
MDL number:
MFCD10566970
Assay:
95% (HPLC)

Key Documents

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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)

SMILES string

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

InChI key

RTHQDNQOODHVLK-UHFFFAOYSA-N

assay

95% (HPLC)

reaction suitability

reagent type: cross-linking reagent

functional group

Fmoc, amine, carboxylic acid

storage temp.

−20°C

Quality Level

100

Related Categories

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

Regulatory Information

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Certificates of Analysis (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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