Purity | Size | Price | VIP Price | USA Stock *0-1 Day | Global Stock *5-7 Days | Quantity | |||||
{[ item.p_purity ]} | {[ item.pr_size ]} |
{[ getRatePrice(item.pr_usd, 1,1) ]} {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate) ]} |
{[ getRatePrice(item.pr_usd, 1,1) ]} | Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate) ]} {[ getRatePrice(item.pr_usd,1,item.mem_rate) ]} | {[ item.pr_usastock ]} | Inquiry - | {[ item.pr_chinastock ]} | Inquiry - |
* Storage: {[proInfo.prStorage]}
CAS No. : | 23024-29-5 | MDL No. : | MFCD00216005 |
Formula : | C18H24N2O8 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | XPKIVYVYXKPGBP-UHFFFAOYSA-N |
M.W : | 396.39 | Pubchem ID : | 3430836 |
Synonyms : |
Disuccinimidyl sebacate;DSSeb;DSSeb Crosslinker, DSSeb Cross linker, DSSeb Cross-linker;Sebacic acid bis N-succinimidyl ester
|
Chemical Name : | Bis(2,5-dioxopyrrolidin-1-yl) decanedioate |
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H315-H319-H335 | Packing Group: | N/A |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With dicyclohexyl-carbodiimide In tetrahydrofuran | ||
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In acetone at 25℃; for 24h; | Experimental General procedure: NHS-Cn was prepared as described by Chen et al. (2011) with a small modification; end-bit binary acid (15 mmol each; C2, C3, C4, C5, C6, C8, C10, C14) and NHS (40 mmol) were dissolved in acetone (25 mL), and then EDC (30 mmol) was added to the solution. The clear mixture was gently stirred at 25°C for 24 h. After the acetone was removed by rotary evaporation under reduced pressure, the residue was washed several times with deionised water and then dried under vacuum at 50°C. The crosslinker thus prepared was characterised by the 1H NMR and FT-IR spectra. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With toluene-4-sulfonic acid; triethylamine In chloroform Yield given; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With NaHCO3 In water; dimethyl sulfoxide mixt. of Eu complex and Et3N in DMSO added at room temp. every 30 min tosoln. of disuccinimidyl sebacate in DMSO with stirring; left at room te mp. for 45 min; mixed with soln. of peptide in aq. NaHCO3 (pH 8.7); stirred at room temp. overnight; purified by semi-preparative RP-HPLC; lyophilised; detd. by mass spectra; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With Et3N In dimethyl sulfoxide mixt. of Eu complex and Et3N in DMSO added at room temp. every 30 min tosoln. of disuccinimidyl sebacate in DMSO with stirring; left at room te mp. for 45 min; detd. by mass spectra; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
52% | With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide for 6h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
30% | In N,N-dimethyl-formamide at 20℃; for 1h; | |
30% | In N,N-dimethyl-formamide at 20℃; for 1h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: N,N-dimethyl-formamide / 1 h / 20 °C 2: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide | ||
Multi-step reaction with 2 steps 1: N,N-dimethyl-formamide / 1 h / 20 °C 2: trifluoroacetic acid / dichloromethane / 2 h / 0 - 20 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 3 steps 1: N,N-dimethyl-formamide / 1 h / 20 °C 2: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 20 °C 3: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide | ||
Multi-step reaction with 3 steps 1: N,N-dimethyl-formamide / 1 h / 20 °C 2: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 0 - 20 °C 3: trifluoroacetic acid / dichloromethane / 2 h / 0 - 20 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: N,N-dimethyl-formamide / 1 h / 20 °C 2: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 20 °C | ||
Multi-step reaction with 2 steps 1: N,N-dimethyl-formamide / 1 h / 20 °C 2: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 0 - 20 °C |
[ 14565-47-0 ]
2,5-Dioxopyrrolidin-1-yl dodecanoate
Similarity: 1.00
[ 14464-32-5 ]
2,5-Dioxopyrrolidin-1-yl stearate
Similarity: 1.00
[ 240133-34-0 ]
2,5-Dioxopyrrolidin-1-yl 4-palmitamidobutanoate
Similarity: 1.00
[ 69888-86-4 ]
2,5-Dioxopyrrolidin-1-yl tetradecanoate
Similarity: 1.00
[ 14464-30-3 ]
2,5-Dioxopyrrolidin-1-yl octanoate
Similarity: 1.00
[ 14565-47-0 ]
2,5-Dioxopyrrolidin-1-yl dodecanoate
Similarity: 1.00
[ 14464-32-5 ]
2,5-Dioxopyrrolidin-1-yl stearate
Similarity: 1.00
[ 240133-34-0 ]
2,5-Dioxopyrrolidin-1-yl 4-palmitamidobutanoate
Similarity: 1.00
[ 69888-86-4 ]
2,5-Dioxopyrrolidin-1-yl tetradecanoate
Similarity: 1.00
[ 14464-30-3 ]
2,5-Dioxopyrrolidin-1-yl octanoate
Similarity: 1.00
[ 14464-31-4 ]
Palmitic acid N-hydroxysuccinimide ester
Similarity: 1.00
[ 240133-34-0 ]
2,5-Dioxopyrrolidin-1-yl 4-palmitamidobutanoate
Similarity: 1.00
[ 69888-86-4 ]
2,5-Dioxopyrrolidin-1-yl tetradecanoate
Similarity: 1.00
[ 146004-84-4 ]
18-((2,5-Dioxopyrrolidin-1-yl)oxy)-18-oxooctadecanoic acid
Similarity: 1.00
[ 159350-38-6 ]
10-((2,5-Dioxopyrrolidin-1-yl)oxy)-10-oxodecanoic acid
Similarity: 1.00