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55750-63-5

55750-63-5 Structure

55750-63-5 Structure
IdentificationMore
[Name]

N-Succinimidyl 6-maleimidohexanoate
[CAS]

55750-63-5
[Synonyms]

6-MALEIMIDOCAPROIC ACID N-SUCCINIMIDYL ESTER
EMCS
EPSILON-MALEIMIDOCAPROIC ACID N-HYDROXYSUCCINIMIDE ESTER
N-(6-MALEIMIDOCAPROYLOXY)SUCCINIMIDE
N-(E-MALEIMIDOCAPROYLOXY)SUCCINIMIDE
N-(EPSILON-MALEIMIDOCAPROYLOXY)SUCCINIMIDE
N-[EPSILON-MALEIMIDOCAPROYLOXY]SUCCINIMIDE ESTER
N-SUCCINIMIDYL 6-MALEIMIDOCAPROATE
N-SUCCINIMIDYL 6-MALEIMIDOHEXANOATE
6-Maleimidohexanoic acid N-hydroxysuccinimide ester
N-SUCCINIMIDYL-6-MALEMIDOCAPROATE, 99%
EPISILON-MALEIMIDOCAPROIC ACID N-*HYDROX YSUCCINIMID
6-maleimidohexanoic acid n-succinimidyl ester
N-(6-Maleimidocaproyloxy)succinimideN-Succinimidyl-6-maleimidohexanoate
6-Maleimidocaproic acid N-hydroxysuccinimide ester
N-Succinimidyl 6-Maleimidohexanoate [Cross-linking Reagent]
6-Maleimidocaproic acid N-succinimidyl ester, N-(ε-Maleimidocaproyloxy)succinimide, N-Succinimidyl 6-maleimidocaproate, EMCS
6-Maleimidohexanoic acid N-hydroxy succinimidyl ester
[EINECS(EC#)]

637-238-5
[Molecular Formula]

C14H16N2O6
[MDL Number]

MFCD00043043
[Molecular Weight]

308.29
[MOL File]

55750-63-5.mol
Chemical PropertiesBack Directory
[Appearance]

White to cream colored crystals
[Melting point ]

70-73 °C(lit.)
[Boiling point ]

480.6±47.0 °C(Predicted)
[density ]

1.40±0.1 g/cm3(Predicted)
[storage temp. ]

−20°C
[solubility ]

chloroform: 100mg/mL
[form ]

powder
[pka]

-2.21±0.20(Predicted)
[color ]

Off-white to pale brown
[Sensitive ]

Light & Moisture Sensitive & Hygroscopic
[BRN ]

1499815
[InChI]

InChI=1S/C14H16N2O6/c17-10-5-6-11(18)15(10)9-3-1-2-4-14(21)22-16-12(19)7-8-13(16)20/h5-6H,1-4,7-9H2
[InChIKey]

VLARLSIGSPVYHX-UHFFFAOYSA-N
[SMILES]

N1(CCCCCC(ON2C(=O)CCC2=O)=O)C(=O)C=CC1=O
[CAS DataBase Reference]

55750-63-5(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xn,Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
R40:Limited evidence of a carcinogenic effect.
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37:Wear suitable protective clothing and gloves .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[F ]

8-10-21
[HS Code ]

29280000
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Description]

Mal-heptanoic NHS ester contains a maleimide group and an NHS ester. The NHS ester can be used to label the primary amines (-NH2) of proteins, amine-modified oligonucleotides, and other amine-containing molecules. The maleimide group will react with a thiol group to form a covalent bond, enabling the connection of biomolecule with a thiol.
[Chemical Properties]

White to cream colored crystals
[Uses]

6-Maleimidohexanoic acid N-hydroxysuccinimide ester can be used in:
  • Synthesis of maleimide-activated carbohydrates for site-specific glycosylation of cysteine-containing peptides and proteins via maleimide-thiol ligation reaction.
  • Synthesis of a glucuronide prodrug of doxorubicin bearing a maleimide side chain as an antitumor agent.
  • Cross-linking oligonucleotides with the amino groups on the substrate to fabricate DNA microarrays.

[reaction suitability]

reagent type: linker
[Synthesis]

N-Hydroxysuccinimide

6066-82-6

6-Maleimidocaproic acid

55750-53-3

N-Succinimidyl 6-maleimidohexanoate

55750-63-5

Under nitrogen protection, 4.7 g (22 mmol) of 6-maleimidohexanoic acid (MC) and 25 g (22 mmol) of N-hydroxybutanediimide (HOSu) were dissolved in 50 ml of acetonitrile. Another 4.5 g (22 mmol) of N,N'-dicyclohexylcarbodiimide (DCC) was dissolved in 25 ml of acetonitrile and the internal temperature was maintained. The DCC solution was slowly added dropwise to the reaction mixture at 0°C. The reaction mixture was stirred at 0 °C for 2 h. The reaction was then brought to room temperature and continued overnight. After completion of the reaction, the precipitate was removed by filtration and the filter cake was washed with acetonitrile (10 ml x 3). The filtrates were combined and concentrated to dryness under reduced pressure. The resulting oily product was dried under reduced pressure for 6 h at room temperature to give 6.4 g of a light brown solid, i.e., succinimidyl 6-(maleimido)hexanoate, in 95% yield.

[IC 50]

Non-cleavable Linker
[References]

[1] Patent: CN107789630, 2018, A. Location in patent: Paragraph 0064; 0065; 0066
[2] Patent: WO2018/178060, 2018, A1. Location in patent: Page/Page column 58; 60; 61
[3] International Journal of Molecular Sciences, 2017, vol. 18, # 9,
[4] Patent: WO2015/95953, 2015, A1. Location in patent: Page/Page column 118
[5] Patent: WO2016/41082, 2016, A1. Location in patent: Page/Page column 97; 98
Spectrum DetailBack Directory
[Spectrum Detail]

N-Succinimidyl 6-maleimidohexanoate(55750-63-5)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

55750-63-5(sigmaaldrich)
[TCI AMERICA]

N-Succinimidyl 6-Maleimidohexanoate  [Cross-linking Reagent],>98.0%(N)(55750-63-5)
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