analytical standard 分析用標準物質 ベースライン干渉を最小限に抑える必要がある、感度の高いクロマトグラフィーおよび分析ワークフロー向け。
Store at -20°C,Desiccated Ice chest + Ice pads に出荷。正確な仕様については、ロット固有の COA をご確認ください。
SDS、COA、データシート、仕様書をダウンロードできます。ロット固有の COA はロット番号検索で入手可能です。
クロマトグラフィー、有機合成、クロスカップリング反応に関する 5638 件の査読済み論文で引用されています。
EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms an amine-reactive O-acylisourea intermediate that quickly reacts with an amino group to form an amide bond with release of an isourea by-product. The intermediate is unstable in aqueous solutions and so two-step conjugation procedures rely on N-hydroxysuccinimide (NHS) for stabilization. Failure to react with an amine will result in hydrolysis of the intermediate, regeneration of the carboxyl, and release of an N-substituted urea. A side reaction is the formation of an N-acylurea, which is usually restricted to carboxyls located in hydrophobic regions of proteins.
Characteristics of EDC:
• Reactive group:carbodiimide
• Reaction target: activates carboxyl groups to conjugate to amino groups (primary amines)
• Several conjugation strategies—react EDC alone with target groups or includecarbodiimide
• Reactivity: Forms active intermediate with carboxyl groups at pH 4.7–6.0 (optimum), then intermediate reacts with primary amines
危険性、取扱い、保管、および規制遵守を網羅した包括的な文書。
<<<<<<< HEAD SDS をダウンロード → ======= SDS をダウンロード → >>>>>>> release248-p3Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic nitrogen compounds |
| 分類 | Organonitrogen compounds |
| Subclass | Amines |
| Intermediate Tree Nodes | Tertiary amines |
| Direct Parent | Trialkylamines |
| Alternative Parents | Propargyl-type 1,3-dipolar organic compounds Carbodiimides Organopnictogen compounds Hydrochlorides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Tertiary aliphatic amine - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carbodiimide - Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - Aliphatic acyclic compound |
| 説明 | This compound belongs to the class of organic compounds known as trialkylamines. These are organic compounds containing a trialkylamine group, characterized by exactly three alkyl groups bonded to the amino nitrogen. |
| External Descriptors | Not available |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | 日付 | 商品 |
|---|---|---|---|
 D2613150 | Certificate of Analysis | Apr 14, 2026 | A638729 |
| D2613152 | Certificate of Analysis | Apr 14, 2026 | A638729 |
| D2613153 | Certificate of Analysis | Apr 14, 2026 | A638729 |
| D2613154 | Certificate of Analysis | Apr 14, 2026 | A638729 |
| D2613171 | Certificate of Analysis | Apr 14, 2026 | A638729 |
| H2420498 | Certificate of Analysis | Aug 22, 2024 | A638729 |
| H2420556 | Certificate of Analysis | Aug 22, 2024 | A638729 |
| I2511038 | Certificate of Analysis | Aug 22, 2024 | A638729 |
| J2422272 | Certificate of Analysis | Aug 22, 2024 | A638729 |
| J2429232 | Certificate of Analysis | Aug 22, 2024 | A638729 |
| K2407241 | Certificate of Analysis | Aug 22, 2024 | A638729 |
| 溶解度 | Water |
|---|---|
| 融点（°C） | 115-118°C |
| 分子量 | 191.700 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 5 |
| Exact Mass | 191.119 Da |
| Monoisotopic Mass | 191.119 Da |
| Topological Polar Surface Area | 28.000 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 134.000 |
| 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 | 2 |
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