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HCID 13007Erstellt: 26. Oktober 2026

1-Ethylpiperidin

N-ETHYLPIPERIDINE · Ethylpiperidine · Piperidine, 1-ethyl- · NSC 2090 · N-Ethylpiperidin · 1-Ethylpiperidin · 1-Ethylpiperidene · 1-ethvlpiperidine

https://huagongshe.com/de/chemical/13007

Molekülstruktur von 1-Ethylpiperidin

Identifikatoren & physikalische Daten

CAS No.766-09-6
SummenformelC7H15N
Durchschnittliche Molmasse113,2 g/mol
Monoisotopische Masse113,12044948 g/mol
SMILESCCN1CCCCC1
InChIKeyHTLZVHNRZJPSMI-UHFFFAOYSA-N
PubChem CID13007
ChEMBLCHEMBL25053
ChEBICHEBI:39017
EC No.212-161-6
DTXSIDDTXSID1061102
Lokaler Name1-Ethylpiperidin

Chemische & physikalische Eigenschaften

XLogP2
Polarare Oberfläche (TPSA)3,2
H-Brücken-Donoren0
H-Brücken-Akzeptoren1
Frei drehbare Bindungen1
Schwere Atome8
Formalladung0
Komplexität55,4
StoffklassenFlammable agents - 3rd degree
SpringerMaterials Properties15N nuclear magnetic resonance spectrum
LogP (Verteilungskoeffizient)1.88
Physical Description1-ethylpiperidine appears as a colorless liquid with the odor of pepper. Less dense than water. May irritate skin and eyes. Vapors heavier than air. Used as a solvent and to make other chemicals.
Schmelzpunkt-20 °C
Siedepunkt131 °C(lit.)
Dichte0.824 g/mL at 25 °C(lit.)
Dampfdruck12.76hPa at 20℃
Brechungsindexn20/D 1.444(lit.)
Flammpunkt66 °F
LagerbedingungenFlammables area
Löslichkeit1-ethylpiperidine salt of benzylpenicillin is considerably less soluble in amyl acetate and acetone.50 G/L
pKa (Säurekonstante)10.45(at 23℃)
AggregatzustandLiquid
FarbeClear colorless to slightly yellow
pH12.2 (50g/l, H2O, 20℃)
Explosionsgrenze1.9-12.1%(V)
BRN102643
Henry-Konstante3.9×10-1 mol/(m3Pa) at 25℃, Hilal et al. (2008)
InChI1S/C7H15N/c1-2-8-6-4-3-5-7-8/h2-7H2,1H3
InChIKeyHTLZVHNRZJPSMI-UHFFFAOYSA-N
SMILESCCN1CCCCC1
LogP (Verteilungskoeffizient)1.89 at 25℃
CAS Datenbank766-09-6(CAS DataBase Reference)
NIST chemische InformationenPiperidine, 1-ethyl-(766-09-6)
EPA chemische InformationenPiperidine, 1-ethyl- (766-09-6)

Sicherheit & Vorschriften

GHS-EinstufungDangerH225 (100%): Highly Flammable liquid and vapor [Danger Flammable liquids]P210, P233, P240, P241, P242, P243, P260, P261, P264, P264+P265, P270, P271, P280, P301+P316, P301+P317, P301+P330+P331, P302+P352, P302+P361+P354, P303+P361+P353, P304+P340, P305+P351+P338, P305+P354+P338, P316, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P363, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 213 reports by companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Regulatorische InformationenChemical: Piperidine, 1-ethyl-Piperidine, 1-ethyl- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Piperidine, 1-ethyl- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)Status: Active Update: 16-05-2018 https://echa.europa.eu/registration-dossier/-/registered-dossier/11076Piperidine, 1-ethyl-: HSNO Approval: HSR001045 Approved with controlsThe New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)
DOT-KennzeichnungFlammable Liquid Corrosive
BrandgefahrenExcerpt from ERG Guide 132 [Flammable Liquids - Corrosive]:· Flammable/combustible material.
GesundheitsgefahrenExcerpt from ERG Guide 132 [Flammable Liquids - Corrosive]:· May cause toxic effects if inhaled or ingested.
DOT-Nummer und Handbuch2386 132
Reaktive GruppeAmines, Phosphines, and Pyridines
Reactivity AlertsHighly Flammable
Reactivity Profile1-ETHYLPIPERIDINE neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides.
DOT Hazard Classification1-EthylpiperidineUN2386Class 3 Flammable and combustible liquid (49 eCFR § 173.120)PG II: the degree of danger presented by the material is medium
Air and Water ReactionsHighly flammable. Soluble in water.
Hazard Classes and CategoriesFlam. Liq. 2 (100%)Flammable agents - 3rd degree
BrandbekämpfungExcerpt from ERG Guide 132 [Flammable Liquids - Corrosive]:
Freisetungsmaßnahmen· CALL 911. Then call emergency response telephone number on shipping paper. If shipping paper not available or no answer, refer to appropriate telephone number listed on the inside back cover.· ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.
Erste HilfeExcerpt from ERG Guide 132 [Flammable Liquids - Corrosive]:General First Aid:
Expositionsschutz und Persönliche Schutzausrüstung· Wear positive pressure self-contained breathing apparatus (SCBA).
Freisetung ohne BrandExcerpt from ERG Guide 132 [Flammable Liquids - Corrosive]:
Isolation and EvacuationExcerpt from ERG Guide 132 [Flammable Liquids - Corrosive]:Immediate precautionary measure
Personal Protective Equipment (PPE)Excerpt from ERG Guide 132 [Flammable Liquids - Corrosive]:
Emergency Response Planning Guidelines· Some of these materials may react violently with water.
F10-23
Wassergefährdungsklasse (WGK)1
TSCA-Inventar-StatusTSCA listed
UN-TransportnummerUN 2386
Zollcode29333990
RTECS-Nr.TN0250000
R-Sätze (R)11-20/22-36/37/38
GefahrensymboleF,Xn
Sicherheitshinweise (S)26-36/37/39
Gefahrenklasse3Acute Tox. 3 InhalationAcute Tox. 3 OralAcute Tox. 4 DermalEye Dam. 1Flam. Liq. 2Skin Corr. 1B
VerpackungsgruppeII
Lagerklasse3 - Flammable liquids

Anwendungen & Verwendung

Verwenden

In Room temperature phosphorescence of α-bromonaphthalene induced by cyclodextrin in the presence of hexahydropyridine or 1-ethylpiperidine and its application is described. The highest yields of 5-Bromopyrimidine (37%) were obtained by using 1-ethylpiperidine or triethylamine as condensing agent. Tributyltin hydride and 1-ethylpiperidine hypophosphite were mediated intermolecular radical additions to 2, 4, 6-trichlorophenyl vinyl sulfonate.