HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Methoxybenzenecarboximidamide
4-MethoxybenziMidaMide · 4-Methoxyl-benzamidine · Benzenecarboximidamide, 4-methoxy- · 4-Methoxybenzamidine for fluorescence · 4-METHOXYBENZAMIDINE FOR FLUORESCENCE 97+%

Identifikatoren & physikalische Daten
| CAS No. | 22265-37-8 |
|---|---|
| Summenformel | C8H10N2O |
| Durchschnittliche Molmasse | 150,18 g/mol |
| Monoisotopische Masse | 150,07931294 g/mol |
| SMILES | COc1ccc(C(=N)N)cc1 |
| InChIKey | CSISQILZUHMAJB-UHFFFAOYSA-N |
| PubChem CID | 229074 |
| ChEMBL | CHEMBL3138844 |
| EC No. | 622-603-3 |
| DTXSID | DTXSID20281672 |
Chemische & physikalische Eigenschaften
| XLogP | 0,9 |
|---|---|
| Polarare Oberfläche (TPSA) | 59,1 |
| H-Brücken-Donoren | 2 |
| H-Brücken-Akzeptoren | 2 |
| Frei drehbare Bindungen | 2 |
| Schwere Atome | 11 |
| Formalladung | 0 |
| Komplexität | 139 |
| Schmelzpunkt | 120-124 °C |
| Lagerbedingungen | Keep in dark place,Inert atmosphere,Room temperature |
| BRN | 637173 |
| InChI | 1S/C8H10N2O/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5H,1H3,(H3,9,10) |
| InChIKey | CSISQILZUHMAJB-UHFFFAOYSA-N |
| SMILES | COc1ccc(cc1)C(N)=N |
Sicherheit & Vorschriften
| GHS-Einstufung | DangerH314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]P260, P264, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P363, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 39 reports by companies from 1 notifications to the ECHA C&L Inventory. |
|---|---|
| Hazard Classes and Categories | Skin Corr. 1B (100%) |
| F | 10-34 |
| Wassergefährdungsklasse (WGK) | 3 |
| UN-Transportnummer | UN 3263 8/PG 3 |
| R-Sätze (R) | 34 |
| Gefahrensymbole | C |
| Sicherheitshinweise (S) | 26-36/37/39-45 |
| Lagerklasse | 8B - Non-combustible corrosive hazardous materials |
| Gefahrenklasse | Skin Corr. 1B |
Anwendungen & Verwendung
Verwenden
Reagent for the determination of reducing carbohydrates and glycoproteins by postcolumn derivatization after HPLC; A method using benzamidine should be improved by this reagent