QBD10213
Fmoc-N-amido-dPEG®4-acid
Manufacturer: Sigma Aldrich
CAS Number: 557756-85-1
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 100 MG | QBD10213-100-MG | In Stock | ₹ 9,634.25 |
| 1000 MG | QBD10213-1000-MG | In Stock | ₹ 24,702.65 |
QBD10213 - 100 MG
In Stock
Quantity
1
Base Price: ₹ 9,634.25
GST (18%): ₹ 1,734.165
Total Price: ₹ 11,368.415
Assay
>90%
form
solid or viscous liquid
reaction suitability
reaction type: Pegylationsreagent type: cross-linking reagent
functional group
Fmocaminecarboxylic acid
polymer architecture
shape: linearfunctionality: heterobifunctional
shipped in
ambient
storage temp.
−20°C
SMILES string
OC(CCOCCOCCOCCOCCNC(OCC1C(C=CC=C2)=C2C3=C1C=CC=C3)=O)=O
InChI
1S/C26H33NO8/c28-25(29)9-11-31-13-15-33-17-18-34-16-14-32-12-10-27-26(30)35-19-24-22-7-3-1-5-20(22)21-6-2-4-8-23(21)24/h1-8,24H,9-19H2,(H,27,30)(H,28,29)
InChI key
NUHRPLKTAAVHCZ-UHFFFAOYSA-N
Other Options
Related Products
Description
- Features and Benefits: Fmoc-N-amido-dPEG®4-acid is a novel Fmoc-protected amino acid containing a single molecular weight PEG (dPEG®) spacer arm. These reagents are used to introduce a hydrophilic, non-immunogenic spacer into a peptide. Three different lengths of dPEG® allow precise control of spacing and hydrophilicity. The Fmoc group can be removed, exposing the terminal amine, using piperidine as with standard peptide synthesis.Fmoc-N-amido-dPEG®n-acid reagents are novel Fmoc-protected amino acids containing a single molecular weight PEG (dPEG®) spacer arm (18.1 Å). This reagents is used to introduce a hydrophilic, non-immunogenic spacer into a peptide. Fmoc group can be removed, exposing the terminal amine, using piperidine as with standard peptide synthesis.
- Legal Information: Products Protected under U.S. Patents # 7,888,536 B2
SAFETY INFORMATION
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Compare Similar Items
Show Difference
Assay: >90%
form: solid or viscous liquid
reaction suitability: reaction type: Pegylationsreagent type: cross-linking reagent
functional group: Fmocaminecarboxylic acid
polymer architecture: shape: linearfunctionality: heterobifunctional
shipped in: ambient
storage temp.: −20°C
SMILES string: OC(CCOCCOCCOCCOCCNC(OCC1C(C=CC=C2)=C2C3=C1C=CC=C3)=O)=O
InChI: 1S/C26H33NO8/c28-25(29)9-11-31-13-15-33-17-18-34-16-14-32-12-10-27-26(30)35-19-24-22-7-3-1-5-20(22)21-6-2-4-8-23(21)24/h1-8,24H,9-19H2,(H,27,30)(H,28,29)
InChI key: NUHRPLKTAAVHCZ-UHFFFAOYSA-N
Assay:
>90%
form:
solid or viscous liquid
reaction suitability:
reaction type: Pegylationsreagent type: cross-linking reagent
functional group:
Fmocaminecarboxylic acid
polymer architecture:
shape: linearfunctionality: heterobifunctional
shipped in:
ambient
storage temp.:
−20°C
SMILES string:
OC(CCOCCOCCOCCOCCNC(OCC1C(C=CC=C2)=C2C3=C1C=CC=C3)=O)=O
InChI:
1S/C26H33NO8/c28-25(29)9-11-31-13-15-33-17-18-34-16-14-32-12-10-27-26(30)35-19-24-22-7-3-1-5-20(22)21-6-2-4-8-23(21)24/h1-8,24H,9-19H2,(H,27,30)(H,28,29)
InChI key:
NUHRPLKTAAVHCZ-UHFFFAOYSA-N
Assay: >90%
form: solid or viscous liquid
reaction suitability: reagent type: cross-linking reagentreactivity: amine reactive
functional group: __
polymer architecture: shape: linearfunctionality: homobifunctional
shipped in: ambient
storage temp.: −20°C
SMILES string: O=C(ON1C(CCC1=O)=O)CCOCCOCCOCCOCCOCCOCCOCCOCCOCCC(ON2C(CCC2=O)=O)=O
InChI: __
InChI key: __
Assay:
>90%
form:
solid or viscous liquid
reaction suitability:
reagent type: cross-linking reagentreactivity: amine reactive
functional group:
__
polymer architecture:
shape: linearfunctionality: homobifunctional
shipped in:
ambient
storage temp.:
−20°C
SMILES string:
O=C(ON1C(CCC1=O)=O)CCOCCOCCOCCOCCOCCOCCOCCOCCOCCC(ON2C(CCC2=O)=O)=O
InChI:
__
InChI key:
__
Assay: >90%
form: solid or viscous liquid
reaction suitability: reagent type: chemical modification reagentreagent type: cross-linking reagentreactivity: amine reactive
functional group: __
polymer architecture: shape: linearfunctionality: monofunctional
shipped in: ambient
storage temp.: −20°C
SMILES string: O=C(CCOCCOCCOCCOCCOCCOCCOCCOC)ON1C(CCC1=O)=O
InChI: 1S/C22H39NO12/c1-27-6-7-29-10-11-31-14-15-33-18-19-34-17-16-32-13-12-30-9-8-28-5-4-22(26)35-23-20(24)2-3-21(23)25/h2-19H2,1H3
InChI key: IBZNTYBFTKFSMU-UHFFFAOYSA-N
Assay:
>90%
form:
solid or viscous liquid
reaction suitability:
reagent type: chemical modification reagentreagent type: cross-linking reagentreactivity: amine reactive
functional group:
__
polymer architecture:
shape: linearfunctionality: monofunctional
shipped in:
ambient
storage temp.:
−20°C
SMILES string:
O=C(CCOCCOCCOCCOCCOCCOCCOCCOC)ON1C(CCC1=O)=O
InChI:
1S/C22H39NO12/c1-27-6-7-29-10-11-31-14-15-33-18-19-34-17-16-32-13-12-30-9-8-28-5-4-22(26)35-23-20(24)2-3-21(23)25/h2-19H2,1H3
InChI key:
IBZNTYBFTKFSMU-UHFFFAOYSA-N
Assay: >90%
form: solid or viscous liquid
reaction suitability: reagent type: chemical modification reagentreagent type: cross-linking reagentreactivity: amine reactive
functional group: __
polymer architecture: shape: linearfunctionality: monofunctional
shipped in: ambient
storage temp.: −20°C
SMILES string: COCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCC(ON1C(CCC1=O)=O)=O
InChI: __
InChI key: __
Assay:
>90%
form:
solid or viscous liquid
reaction suitability:
reagent type: chemical modification reagentreagent type: cross-linking reagentreactivity: amine reactive
functional group:
__
polymer architecture:
shape: linearfunctionality: monofunctional
shipped in:
ambient
storage temp.:
−20°C
SMILES string:
COCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCC(ON1C(CCC1=O)=O)=O
InChI:
__
InChI key:
__