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≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Amino-PEG2-t-Boc-Hydrazide is a PEG derivative containing an amino group and a Boc-protected hydrazide. The hydrophilic PEG spacer increases solubility in aqueous media. The amino group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The Boc can be deprotected under mild acidic conditions to form a reactive hydrazide, which can then be coupled with various carbonyl groups.
| Canonical Smiles | CC(C)(C)OC(=O)NNC(=O)CCOCCOCCN |
|---|---|
| IUPAC Name | tert-butyl N-[3-[2-(2-aminoethoxy)ethoxy]propanoylamino]carbamate |
| InChIKey | UDVYFYDWDLXHPA-UHFFFAOYSA-N |
| INCHI | 1S/C12H25N3O5/c1-12(2,3)20-11(17)15-14-10(16)4-6-18-8-9-19-7-5-13/h4-9,13H2,1-3H3,(H,14,16)(H,15,17) |
| Isomeric SMILES | CC(C)(C)OC(=O)NNC(=O)CCOCCOCCN |
| PubChem CID | 117777156 |
| Molecular Weight | 291.34 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Class | Carboxylic acids and derivatives |
| Subclass | Hydrazinecarboxylic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Hydrazinecarboxylic acid esters |
| Alternative Parents | Organic carbonic acids and derivatives Dialkyl ethers Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Hydrazinecarboxylic acid ester - Carbonic acid derivative - Ether - Dialkyl ether - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as hydrazinecarboxylic acid esters. These are ester derivatives of hydrazinecarboxylic acids. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Oct 16, 2024 | A596403 | |
| Certificate of Analysis | Oct 16, 2024 | A596403 | |
| Certificate of Analysis | Oct 16, 2024 | A596403 | |
| Certificate of Analysis | Oct 16, 2024 | A596403 | |
| Certificate of Analysis | Oct 16, 2024 | A596403 | |
| Certificate of Analysis | Oct 16, 2024 | A596403 |
| Sensitivity | Light Sensitive |
|---|---|
| Molecular Weight | 291.340 g/mol |
| XLogP3 | -0.900 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 10 |
| Exact Mass | 291.179 Da |
| Monoisotopic Mass | 291.179 Da |
| Topological Polar Surface Area | 112.000 Ų |
| Heavy Atom Count | 20 |
| Formal Charge | 0 |
| Complexity | 291.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |