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HCID 24372Erstellt: 26. Oktober 2026
1,2-Diethylhydrazine dihydrochloride
1,2-DIETHYLHYDRAZINE DIHYDROCHLORIDE · 1,2-Diethylhydrazine2HCl · -Diethylhydrazine dihydrochloride · 1,2-diethyl-hydrazindihydrochloride · N,N'-Diethylhydrazine dihydrochloride · Hydrazine, 1,2-diethyl, dihydrochloride. · N,Nzzhlxy-Diethylhydrazine dihydrochloride · N,N''-DIETHYLHYDRAZINE DIHYDROCHLORIDE: TECH., 90%
https://huagongshe.com/de/chemical/24372
Identifikatoren & physikalische Daten
| CAS No. | 7699-31-2 |
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| Summenformel | C4H12N2.2ClH |
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| Durchschnittliche Molmasse | 161,07 g/mol |
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| Monoisotopische Masse | 160,0534038 g/mol |
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| SMILES | CCNNCC.Cl.Cl |
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| InChIKey | NMTDWUVFGOBBAX-UHFFFAOYSA-N |
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| PubChem CID | 24372 |
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| ChEMBL | CHEMBL1203769 |
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| EC No. | 624-628-5 |
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| DTXSID | DTXSID2025056 |
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Chemische & physikalische Eigenschaften
| Polarare Oberfläche (TPSA) | 24,1 |
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| H-Brücken-Donoren | 4 |
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| H-Brücken-Akzeptoren | 2 |
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| Frei drehbare Bindungen | 3 |
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| Schwere Atome | 8 |
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| Formalladung | 0 |
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| Komplexität | 17,5 |
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| Stoffklassen | Nitrogen Compounds -> Hydrazines |
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| Löslichkeit | greater than or equal to 100 mg/mL at 64 °F (NTP, 1992)DMSO, Methanol |
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| Schmelzpunkt | 336 °F (decomposes) (NTP, 1992)169 °C (dec.)(lit.) |
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| Physical Description | 1,2-diethylhydrazine dihydrochloride is a white powder. (NTP, 1992)White solid[CAMEO] White odorless crystalline powder[Alfa Aesar MSDS] |
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| Lagerbedingungen | Room Temperature |
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| Aggregatzustand | Solid |
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| Farbe | Off-White |
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| BRN | 3668380 |
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| InChI | 1S/C4H12N2.2ClH/c1-3-5-6-4-2/h5-6H,3-4H2,1-2H32*1H |
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| InChIKey | NMTDWUVFGOBBAX-UHFFFAOYSA-N |
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| SMILES | Cl[H].Cl[H].CCNNCC |
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| CAS Datenbank | 7699-31-2 |
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| EPA chemische Informationen | 1,2-Diethylhydrazine dihydrochloride (7699-31-2) |
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Sicherheit & Vorschriften
| GHS-Einstufung | DangerH302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]P203, P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P318, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 43 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies. |
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| DOT-Kennzeichnung | Poison |
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| Brandgefahren | Flash point data for this chemical are not available. It is probably combustible. (NTP, 1992) |
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| Gesundheitsgefahren | SYMPTOMS: Symptoms of exposure to this compound may include a burning sensation, coughing, wheezing, laryngitis, shortness of breath, headache, nausea and vomiting. |
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| Gefahrenübersicht | A strong reducing agent[CAMEO] A severe irritant that may cause corrosive injuries at high concentrationsHarmful by ingestion, inhalation, and skin absorption[NTP] A skin and strong eye irritantToxic by ingestion and skin absorption[Alfa Aesar MSDS] |
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| Reaktive Gruppe | Azo, Diazo, Azido, Hydrazine, and Azide Compounds |
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| Reactivity Alerts | Strong Reducing Agent |
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| Reactivity Profile | 1,2-DIETHYLHYDRAZINE DIHYDROCHLORIDE is incompatible with strong oxidizing agents, strong acids and strong bases. (NTP, 1992) |
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| Air and Water Reactions | Probably moisture sensitive. Water soluble. |
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| Hazard Classes and Categories | Acute Tox. 4 (100%) |
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| Brandbekämpfung | Fires involving this material can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992) |
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| Erste Hilfe | EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop. |
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Anwendungen & Verwendung
Verwenden
Reactant involved in:• ;Bromopyridazinedione-mediated protein and peptide bioconjugation1• ;Synthesis of human neutrophil proteinase 3 inhibitors2• ;Three-component cascade processes for sythesis of aminoisoindolones and phthalazones3• ;Stereoselective heterocyclization for synthesis of substituted hexahydropyrazolodiazepinecarboxylates4• ;Synthesis of azacycloalkanes, isoindoles, pyrazole, pyrazolidine, and phthalazine derivatives5