Non-8-en-1-ol
Grundinformationen
- CAS
13038-21-6- Standard-SMILES
C=CCCCCCCCO- InChIKey
FKGFCVJJLGSFSB-UHFFFAOYSA-N- Summenformel
- C9H18O
- Durchschnittliche Molmasse
- 142,24 g/mol
- Monoisotopische Masse
- 142,1357652
Namen und Bezeichner
- Bevorzugter Name
- Non-8-en-1-ol
- IUPAC
- non-8-en-1-ol
- Englischer Name
- 8-NONEN-1-OL
- Summenformel
- C9H18O
- Molmasse
- 142.24
Namen und Synonyme
Non-8-en-1-olRefChem:854442848-942-98-Nonen-1-ol13038-21-6MFCD007980628-nonenol8-nonene-1-olSCHEMBL133623SCHEMBL133624orb2940250SCHEMBL3170179
Weitere Namen anzeigen
8-Nonen-1-ol>8-NONEN-1-OL97+%
DTXSID20454905NAA03821TYD-00328AKOS015839898HY-W127362AS-56400DA-12819SY054507
Datenbank-Bezeichner
- CAS
13038-21-6- PubChem CID
- 11094728
- DTXSID
DTXSID20454905- EC Number
- 848-942-9
- Nikkaji
- J112.180D
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 3,3
- Polarare Oberfläche (TPSA)
- 20,2 Ų
- H-Brücken-Donoren
- 1
- H-Brücken-Akzeptoren
- 1
- Frei drehbare Bindungen
- 7
- Schwere Atome
- 10
- Formalladung
- 0
- Komplexität
- 69,1
Physikochemische Eigenschaften
- Schmelzpunkt
- -7 °C · -7°C (estimate)
- Siedepunkt
- 134 °C · 134 °C / 20mmHg
- Dichte
- 0.85 · 0.85
- Brechungsindex
- 1.444 to · 1.4440 to 1.4470
- storage temp.
- 2 · 2-8°C, stored under nitrogen
- pka
- 15.2 · 15.20±0.10(Predicted)
- Aggregatzustand
- clear liquid
- Farbe
- Colorless to Almost colorless
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Warning
H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.
Gefahrenhinweise
Hazard Classes and CategoriesSkin Irrit. 2 (100%)
Sicherheitsdaten
- hs_code
- 2905.29.9000
- risk_code
- 36/37/38
- safety_code
- 26-36/37/39
Chemie und Industrie
Anwendungen
Verwenden8-Nonen-1-ol is a reactant in the synthesis of chlorosulfolipid (+)-danicalipin A, which has cytotoxicity towards various mammalian cell lines and increases the uptake of fluorophores into bacteria and mammalian cells.
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