Phthalimide Protected Aminooxy Reagents – VectorLabs https://staging.vectorlabs.com From linker design and synthesis, bioconjugated design and manufacturing, biomolecule labeling and functionalization, and detection system and solutions, our team is here to help you move forward, with impact. Wed, 22 Oct 2025 17:20:28 +0000 en-US hourly 1 https://wordpress.org/?v=6.8.3 https://staging.vectorlabs.com/wp-content/uploads/2024/11/V-favicon-02-100x100.png Phthalimide Protected Aminooxy Reagents – VectorLabs https://staging.vectorlabs.com 32 32 Phthalimidooxy-dPEG®₁₂-NHS ester https://staging.vectorlabs.com/products/phthalimidooxy-dpeg12-nhs-ester/ Sat, 24 Feb 2024 02:15:03 +0000 https://staging.vectorlabs.com/?post_type=product&p=37509 Phthalimidooxy-dPEG®12-NHS ester, product number QBD-10011, is a protected aminooxy compound linked to an amine-reactive N-hydroxysuccinimidyl (NHS) ester through a medium-length (41 atoms, 46.3 Å), single molecular weight, discrete polyethylene glycol (dPEG®) spacer. This allows a hydrophilic, protected aminooxy group to be installed on peptides, proteins, small molecules, and amine-functionalized surfaces.

The phthaloyl moiety on phthalimidooxy-dPEG®4-NHS ester stably protects the aminooxy group. Following amide bond formation, the phthalimide group can be removed using aqueous hydrazine or hydroxylamine, leaving the aminooxy group free to react. Oxime bonds form from the reaction between an aminooxy group and an aldehyde (creating an aldoxime bond) or ketone (creating a ketoxime bond). Compared to hydrazone bonds, oxime bonds are exceptionally stable. They do not break under physiological or even slightly acidic conditions that can occur under some physiological states.

The amine-reactive NHS ester has optimal reactivity in the pH range of 7.0 - 7.4. This group should be reacted first as the subsequent deprotection step for the aminooxy group will also react with the NHS ester.

Specifications

Unit Size 100mg, 1000mg
Molecular Weight 860.90; single compound
Chemical formula C₃₉H₆₀N₂O₁₉
CAS N/A
Purity > 97%
Spacers dPEG® Spacer is 41 atoms and 46.3 Å
Shipping Ambient
Typical solubility properties (for additional information contact Customer Support) Methylene chloride or Acetonitrile.
Storage and handling -20°C; Always let come to room temperature before opening; be careful to limit exposure to moisture and restore under an inert atmosphere; stock solutions can be prepared with dry solvent and kept for several days (freeze when not in use). dPEG® pegylation compounds are generally hygroscopic and should be treated as such. This will be less noticeable with liquids, but the solids will become tacky and difficult to manipulate, if care is not taken to minimize air exposure.

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Description

Phthalimidooxy-dPEG®12-NHS ester, product number QBD-10011, is a protected aminooxy compound linked to an amine-reactive N-hydroxysuccinimidyl (NHS) ester through a medium-length (41 atoms, 46.3 Å), single molecular weight, discrete polyethylene glycol (dPEG®) spacer. This allows a hydrophilic, protected aminooxy group to be installed on peptides, proteins, small molecules, and amine-functionalized surfaces.

The phthaloyl moiety on phthalimidooxy-dPEG®4-NHS ester stably protects the aminooxy group. Following amide bond formation, the phthalimide group can be removed using aqueous hydrazine or hydroxylamine, leaving the aminooxy group free to react. Oxime bonds form from the reaction between an aminooxy group and an aldehyde (creating an aldoxime bond) or ketone (creating a ketoxime bond). Compared to hydrazone bonds, oxime bonds are exceptionally stable. They do not break under physiological or even slightly acidic conditions that can occur under some physiological states.

The amine-reactive NHS ester has optimal reactivity in the pH range of 7.0 – 7.4. This group should be reacted first as the subsequent deprotection step for the aminooxy group will also react with the NHS ester.

Specifications

Unit Size100mg, 1000mg
Molecular Weight860.90; single compound
Chemical formulaC₃₉H₆₀N₂O₁₉
CASN/A
Purity> 97%
SpacersdPEG® Spacer is 41 atoms and 46.3 Å
ShippingAmbient
Typical solubility properties (for additional information contact Customer Support)Methylene chloride or Acetonitrile.
Storage and handling-20°C; Always let come to room temperature before opening; be careful to limit exposure to moisture and restore under an inert atmosphere; stock solutions can be prepared with dry solvent and kept for several days (freeze when not in use). dPEG® pegylation compounds are generally hygroscopic and should be treated as such. This will be less noticeable with liquids, but the solids will become tacky and difficult to manipulate, if care is not taken to minimize air exposure.



Documents

References

Greg T. Hermanson, Bioconjugate Techniques, 3rd Edition, Elsevier, Waltham, MA 02451, 2013, ISBN 978-0-12-382239-0; See Chapter 18, Discrete PEG Reagents, pp. 787-821, for a full overview of the dPEG® products.

The post Phthalimidooxy-dPEG®₁₂-NHS ester appeared first on VectorLabs.

]]> Phthalimidooxy-dPEG®₄-NHS ester https://staging.vectorlabs.com/products/phthalimidooxy-dpeg4-nhs-ester/ Sat, 24 Feb 2024 02:04:29 +0000 https://staging.vectorlabs.com/?post_type=product&p=32731 Phthalimidooxy-dPEG®4-NHS ester, product number QBD-10011, is a protected aminooxy compound linked to an amine-reactive N-hydroxysuccinimidyl (NHS) ester through a single molecular weight, discrete polyethylene glycol (dPEG®) spacer. This allows a hydrophilic, protected aminooxy group to be installed on peptides, proteins, small molecules, and amine-functionalized surfaces.

The amine-reactive NHS ester has optimal reactivity in the pH range of 7.0 - 7.4. This group should be reacted first as the subsequent deprotection step for the aminooxy group will also react with the NHS ester.

The phthaloyl moiety on phthalimidooxy-dPEG®4-NHS ester stably protects the aminooxy group. Following amide bond formation, the phthalimide group can be removed using aqueous hydrazine or hydroxylamine, leaving the aminooxy group free to react.

Oxime bonds form from the reaction between an aminooxy group and an aldehyde or ketone. If the formative reaction is between an aminooxy and an aldehyde, the oxime bond formed is called an aldoxime. The oxime bond formed by the reaction of an aminooxy and a ketone is called a ketoxime. Compared to hydrazone bonds, oxime bonds are exceptionally stable. They do not break under physiological or even slightly acidic conditions that can occur under some physiological states.

Specifications

Unit Size 100mg, 1000mg
Molecular Weight 508.48; single compound
Chemical formula C₂₃H₂₈N₂O₁₁
CAS N/A
Purity > 98%
Spacers dPEG® Spacer is 17 atoms and 19.0 Å
Shipping Ambient
Typical solubility properties (for additional information contact Customer Support) Methylene chloride or Acetonitrile.
Storage and handling -20°C; Always let come to room temperature before opening; be careful to limit exposure to moisture and restore under an inert atmosphere; stock solutions can be prepared with dry solvent and kept for several days (freeze when not in use). dPEG® pegylation compounds are generally hygroscopic and should be treated as such. This will be less noticeable with liquids, but the solids will become tacky and difficult to manipulate, if care is not taken to minimize air exposure.

The post Phthalimidooxy-dPEG®₄-NHS ester appeared first on VectorLabs.

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Phthalimidooxy-dPEG®4-NHS ester, product number QBD-10011, is a protected aminooxy compound linked to an amine-reactive N-hydroxysuccinimidyl (NHS) ester through a single molecular weight, discrete polyethylene glycol (dPEG®) spacer. This allows a hydrophilic, protected aminooxy group to be installed on peptides, proteins, small molecules, and amine-functionalized surfaces. Deprotecting the aminooxy group allows the formation of stable oxime bonds with aldehydes and ketones.

Description

Phthalimidooxy-dPEG®4-NHS ester, product number QBD-10011, is a protected aminooxy compound linked to an amine-reactive N-hydroxysuccinimidyl (NHS) ester through a single molecular weight, discrete polyethylene glycol (dPEG®) spacer. This allows a hydrophilic, protected aminooxy group to be installed on peptides, proteins, small molecules, and amine-functionalized surfaces.

The amine-reactive NHS ester has optimal reactivity in the pH range of 7.0 – 7.4. This group should be reacted first as the subsequent deprotection step for the aminooxy group will also react with the NHS ester.

The phthaloyl moiety on phthalimidooxy-dPEG®4-NHS ester stably protects the aminooxy group. Following amide bond formation, the phthalimide group can be removed using aqueous hydrazine or hydroxylamine, leaving the aminooxy group free to react.

Oxime bonds form from the reaction between an aminooxy group and an aldehyde or ketone. If the formative reaction is between an aminooxy and an aldehyde, the oxime bond formed is called an aldoxime. The oxime bond formed by the reaction of an aminooxy and a ketone is called a ketoxime. Compared to hydrazone bonds, oxime bonds are exceptionally stable. They do not break under physiological or even slightly acidic conditions that can occur under some physiological states.

Specifications

Unit Size100mg, 1000mg
Molecular Weight508.48; single compound
Chemical formulaC₂₃H₂₈N₂O₁₁
CASN/A
Purity> 98%
SpacersdPEG® Spacer is 17 atoms and 19.0 Å
ShippingAmbient
Typical solubility properties (for additional information contact Customer Support)Methylene chloride or Acetonitrile.
Storage and handling-20°C; Always let come to room temperature before opening; be careful to limit exposure to moisture and restore under an inert atmosphere; stock solutions can be prepared with dry solvent and kept for several days (freeze when not in use). dPEG® pegylation compounds are generally hygroscopic and should be treated as such. This will be less noticeable with liquids, but the solids will become tacky and difficult to manipulate, if care is not taken to minimize air exposure.

Documents

References

  1. Greg T. Hermanson, Bioconjugate Techniques, 3rd Edition, Elsevier, Waltham, MA 02451, 2013, ISBN 978-0-12-382239-0; See Chapter 18, Discrete PEG Reagents, pp. 787-821, for a full overview of the dPEG® products.

The post Phthalimidooxy-dPEG®₄-NHS ester appeared first on VectorLabs.

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