Cas no 880129-82-8 (Azido-PEG6-CH2COOH)

Azido-PEG6-CH2COOH structure
Azido-PEG6-CH2COOH structure
Product Name:Azido-PEG6-CH2COOH
CAS No:880129-82-8
MF:C14H27N3O8
MW:365.379484415054
CID:3291309
PubChem ID:86229809
Update Time:2024-10-26

Azido-PEG6-CH2COOH Chemical and Physical Properties

Names and Identifiers

    • 3,6,9,12,15,18-HEXAOXAEICOSANOIC ACID, 20-AZIDO-
    • AZIDE-PEG6-CH2COOH
    • N3-PEG6-CH2COOH
    • 20-azido-3,6,9,12,15,18-hexaoxaicosanoic acid
    • Azido-PEG6-CH2COOH
    • 2-[(17-Azido-3,6,9,12,15-pentaoxaheptadec-1-yl)oxy]acetic acid (ACI)
    • 3,6,9,12,15,18-Hexaoxaeicosanoic acid, 20-azido- (9CI)
    • 2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]acetic acid
    • 880129-82-8
    • MS-25832
    • HY-134696
    • AKOS040758427
    • DA-50903
    • CS-0148084
    • SCHEMBL16294246
    • F82834
    • Inchi： 1S/C14H27N3O8/c15-17-16-1-2-20-3-4-21-5-6-22-7-8-23-9-10-24-11-12-25-13-14(18)19/h1-13H2,(H,18,19)
    • InChI Key： GXXXKIVNLFPCAG-UHFFFAOYSA-N
    • SMILES： [N-]=[N+]=NCCOCCOCCOCCOCCOCCOCC(O)=O

Computed Properties

  • Exact Mass: 365.17981483g/mol
  • Monoisotopic Mass: 365.17981483g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 10
  • Heavy Atom Count: 25
  • Rotatable Bond Count: 20
  • Complexity: 353
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -0.2
  • Topological Polar Surface Area: 107?2

Azido-PEG6-CH2COOH Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd.
A936583-100mg
Azido-PEG6-CH2COOH
 880129-82-8 ≥95%
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 ￥1,440.00 2022-09-29
Biosynth
FKB12982-25 mg
20-Azido-3,6,9,12,15,18-hexaoxaicosanoic acid
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FKB12982-100 mg
20-Azido-3,6,9,12,15,18-hexaoxaicosanoic acid
 880129-82-8
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Biosynth
FKB12982-250 mg
20-Azido-3,6,9,12,15,18-hexaoxaicosanoic acid
 880129-82-8
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 $500.00 2023-01-04
Biosynth
FKB12982-500 mg
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 880129-82-8
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MedChemExpress
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Azido-PEG6-CH2COOH
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XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd.
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SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
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Azido-PEG6-CH2COOH Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Trifluoroacetic acid Solvents: Dichloromethane ;  0 °C; 6 h, rt
Reference
Intracellular Protein-Labeling Probes for Multicolor Single-Molecule Imaging of Immune Receptor-Adaptor Molecular Dynamics
Sato, Ryota; et al, Journal of the American Chemical Society, 2017, 139(48), 17397-17404

Production Method 2

Reaction Conditions
1.1 Reagents: Sodium azide Solvents: Dimethylformamide ;  overnight, 70 °C
2.1 Reagents: Sodium hydroxide Solvents: Methanol ,  Water ;  0 °C; 21 h, rt
2.2 Reagents: Hydrochloric acid Solvents: Water ;  pH 2
Reference
Surface-Bound Cytomimetic Assembly Based on Chemoselective and Biocompatible Immobilization and Further Modification of Intact Liposome
Ma, Yong; et al, Bioconjugate Chemistry, 2010, 21(11), 1994-1999

Production Method 3

Reaction Conditions
1.1 Reagents: Sodium azide Solvents: Dimethylformamide ;  12 h, 100 °C
1.2 Solvents: Water
2.1 Reagents: Sodium hydride Solvents: Tetrahydrofuran ;  1 h, 0 °C
2.2 Solvents: Tetrahydrofuran ;  0 °C; 5 min, 0 °C; 16 h, rt
2.3 Solvents: Water ;  cooled
2.4 Reagents: Hydrochloric acid Solvents: Water ;  pH 5
Reference
Design, synthesis and activity study of a novel PI3K degradation by hijacking VHL E3 ubiquitin ligase
Wang, Haili; et al, Bioorganic & Medicinal Chemistry, 2022, 61,

Production Method 4

Reaction Conditions
1.1 Reagents: Dicyclohexylcarbodiimide Solvents: Chloroform ;  30 min, 0 °C
1.2 overnight, rt
2.1 Reagents: Diisopropylethylamine Solvents: Tetrahydrofuran ,  Water ;  8 h, rt
Reference
Surface-Bound Cytomimetic Assembly Based on Chemoselective and Biocompatible Immobilization and Further Modification of Intact Liposome
Ma, Yong; et al, Bioconjugate Chemistry, 2010, 21(11), 1994-1999

Production Method 5

Reaction Conditions
1.1 Reagents: Sodium hydroxide Solvents: Tetrahydrofuran ,  Water ;  rt → 0 °C
1.2 Solvents: Tetrahydrofuran ;  2 h, 0 °C; 3 h, 0 °C
2.1 Reagents: Sodium azide Solvents: Dimethylformamide ;  5 h, 60 °C
3.1 Reagents: Sodium hydride Solvents: Dimethylformamide ;  30 min, cooled
3.2 0 °C; 16 h, rt
3.3 Reagents: Water ;  cooled
4.1 Reagents: Sodium hydroxide Solvents: Methanol ,  Water ;  10 min, rt
4.2 Reagents: Hydrogen ion Solvents: Water ;  pH 3.5
Reference
Towards potential nanoparticle contrast agents: synthesis of new functionalized PEG bisphosphonates
Kachbi-Khelfallah, Souad; et al, Beilstein Journal of Organic Chemistry, 2016, 12, 1366-1371

Production Method 6

Reaction Conditions
1.1 Reagents: Sodium hydroxide Solvents: Methanol ,  Water ;  10 min, rt
1.2 Reagents: Hydrogen ion Solvents: Water ;  pH 3.5
Reference
Towards potential nanoparticle contrast agents: synthesis of new functionalized PEG bisphosphonates
Kachbi-Khelfallah, Souad; et al, Beilstein Journal of Organic Chemistry, 2016, 12, 1366-1371

Production Method 7

Reaction Conditions
1.1 Reagents: Sodium hydroxide Solvents: Methanol ,  Water ;  0 °C; 21 h, rt
1.2 Reagents: Hydrochloric acid Solvents: Water ;  pH 2
Reference
Surface-Bound Cytomimetic Assembly Based on Chemoselective and Biocompatible Immobilization and Further Modification of Intact Liposome
Ma, Yong; et al, Bioconjugate Chemistry, 2010, 21(11), 1994-1999

Production Method 8

Reaction Conditions
1.1 Reagents: Trifluoroacetic acid ;  4 h, rt
Reference
A Y-Shaped Three-Arm Structure for Probing Bivalent Interactions between Protein Receptor-Ligand Using AFM and SPR
Senapati, Subhadip ; et al, Langmuir, 2018, 34(23), 6930-6940

Production Method 9

Reaction Conditions
1.1 Reagents: Sodium hydride Solvents: Tetrahydrofuran ;  1 h, 0 °C
1.2 Solvents: Tetrahydrofuran ;  0 °C; 5 min, 0 °C; 16 h, rt
1.3 Solvents: Water ;  cooled
1.4 Reagents: Hydrochloric acid Solvents: Water ;  pH 5
Reference
Design, synthesis and activity study of a novel PI3K degradation by hijacking VHL E3 ubiquitin ligase
Wang, Haili; et al, Bioorganic & Medicinal Chemistry, 2022, 61,

Production Method 10

Reaction Conditions
1.1 Reagents: Diisopropylethylamine Solvents: Tetrahydrofuran ,  Water ;  8 h, rt
Reference
Surface-Bound Cytomimetic Assembly Based on Chemoselective and Biocompatible Immobilization and Further Modification of Intact Liposome
Ma, Yong; et al, Bioconjugate Chemistry, 2010, 21(11), 1994-1999

Production Method 11

Reaction Conditions
1.1 Reagents: Potassium tert-butoxide Solvents: Tetrahydrofuran ;  5 h, rt
2.1 Reagents: Trifluoroacetic acid ;  4 h, rt
Reference
A Y-Shaped Three-Arm Structure for Probing Bivalent Interactions between Protein Receptor-Ligand Using AFM and SPR
Senapati, Subhadip ; et al, Langmuir, 2018, 34(23), 6930-6940

Production Method 12

Reaction Conditions
1.1 Reagents: Sodium hydride Solvents: Dimethylformamide ;  30 min, 0 °C
1.2 0 °C; 1 h, 0 °C
1.3 Solvents: Water
2.1 Reagents: Trifluoroacetic acid Solvents: Dichloromethane ;  0 °C; 6 h, rt
Reference
Intracellular Protein-Labeling Probes for Multicolor Single-Molecule Imaging of Immune Receptor-Adaptor Molecular Dynamics
Sato, Ryota; et al, Journal of the American Chemical Society, 2017, 139(48), 17397-17404

Production Method 13

Reaction Conditions
1.1 Catalysts: 4-(Dimethylamino)pyridine Solvents: Dichloromethane ,  Pyridine ;  5 h, rt
2.1 Reagents: Sodium azide Solvents: Dimethylformamide ;  overnight, 70 °C
3.1 Reagents: Sodium hydroxide Solvents: Methanol ,  Water ;  0 °C; 21 h, rt
3.2 Reagents: Hydrochloric acid Solvents: Water ;  pH 2
Reference
Surface-Bound Cytomimetic Assembly Based on Chemoselective and Biocompatible Immobilization and Further Modification of Intact Liposome
Ma, Yong; et al, Bioconjugate Chemistry, 2010, 21(11), 1994-1999

Production Method 14

Reaction Conditions
1.1 Reagents: Sodium hydroxide Solvents: Tetrahydrofuran ,  Water ;  5 min, 0 °C; 2 h, rt
2.1 Reagents: Sodium azide Solvents: Dimethylformamide ;  12 h, 100 °C
2.2 Solvents: Water
3.1 Reagents: Sodium hydride Solvents: Tetrahydrofuran ;  1 h, 0 °C
3.2 Solvents: Tetrahydrofuran ;  0 °C; 5 min, 0 °C; 16 h, rt
3.3 Solvents: Water ;  cooled
3.4 Reagents: Hydrochloric acid Solvents: Water ;  pH 5
Reference
Design, synthesis and activity study of a novel PI3K degradation by hijacking VHL E3 ubiquitin ligase
Wang, Haili; et al, Bioorganic & Medicinal Chemistry, 2022, 61,

Production Method 15

Reaction Conditions
1.1 Catalysts: Boron trifluoride etherate Solvents: Dichloromethane ;  0 °C; 15 min, rt
2.1 Catalysts: 4-(Dimethylamino)pyridine Solvents: Dichloromethane ,  Pyridine ;  5 h, rt
3.1 Reagents: Sodium azide Solvents: Dimethylformamide ;  overnight, 70 °C
4.1 Reagents: Sodium hydroxide Solvents: Methanol ,  Water ;  0 °C; 21 h, rt
4.2 Reagents: Hydrochloric acid Solvents: Water ;  pH 2
Reference
Surface-Bound Cytomimetic Assembly Based on Chemoselective and Biocompatible Immobilization and Further Modification of Intact Liposome
Ma, Yong; et al, Bioconjugate Chemistry, 2010, 21(11), 1994-1999

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