Piperidine

HCID 178730326CAS 52167-54-1

Basic information

Standard SMILES
C1CCNCC1
InChIKey
NQRYJNQNLNOLGT-UHFFFAOYSA-N
Molecular formula
C5H11N
Average molar mass
85.15 g/mol

Overview

Piperidine appears as a clear colorless liquid with a pepper-like odor. Less dense than water, but miscible in water. Will float on water. Flash point 37 °F. Melting point -15.8 °F (-9 °C). Boiling point 222.8 °F (106 °C). May severely irritate skin and eyes. May be toxic by ingestion and inhalation. Vapors heavier than air. Used to make rubber and as a solvent.

Names & identifiers

Preferred name
Piperidine
IUPAC
piperidine
English name
piperidine
Molecular formula
C12H19NO3S
Molecular weight
0

Names & synonyms

PIPERIDINE110-89-4HexahydropyridineCyclopentimineAzacyclohexaneHexazaneCypentilPentamethyleneiminePiperidinPentamethyleniminePerhydropyridinePyridine, hexahydro-
Show more names
FEMA No. 2908DTXSID602116567I85E138YDTXCID101165CHEBI:18049RefChem:6144203-813-0Pentamethyleneamine

Database identifiers

CAS
52167-54-1
ChEMBL
CHEMBL15487
ChEBI
CHEBI:18049
UNII
67I85E138Y
EC Number
203-813-0
Nikkaji
J2.884C

Properties

Computed structural properties

XLogP
0.8
Topological polar surface area
12 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
1
Rotatable bonds
0
Heavy atoms
6

Experimental & physicochemical properties

Chemical Classes · 2 items

Nitrogen Compounds -> Amines, Cyclic

Flammable agents - 3rd degree

pHStrong base
SpringerMaterials Properties15N nuclear magnetic resonance spectrum
FragrancesFragrance Ingredient (Piperidine) -> IFRA transparency List
LogP · 4 items

log Kow = 0.84

0.84

0.84

0.84

Odor · 3 items

AMINE-LIKE ODOR

HEAVY, SWEET, FLORAL, ANIMAL ODOR

Odor of pepper

Safety & regulation

GHS classification

GHS Classification · 6 items

Danger

H225: Highly Flammable liquid and vapor [Danger Flammable liquids]

P210, P233, P240, P241, P242, P243, P260, P261, P262, P264, P270, P271, P280, P301+P330+P331, P302+P352, P302+P361+P354, P303+P361+P353, P304+P340, P305+P354+P338, P316, P321, P361+P364, P363, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)

Danger

H225 (100%): Highly Flammable liquid and vapor [Danger Flammable liquids]

P210, P233, P240, P241, P242, P243, P260, P261, P262, P264, P270, P271, P280, P301+P317, P301+P330+P331, P302+P352, P302+P361+P354, P303+P361+P353, P304+P340, P305+P354+P338, P316, P321, P330, P361+P364, P363, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)

Hazard information

Regulatory Information · 6 items

Chemical: Piperidine

List I Chemical: A chemical specified by regulation that, in addition to legitimate uses, is used in manufacturing a controlled substance in violation of the Act and is important to the manufacture of a controlled substance. (21 eCFR 1310.02)

Regulation (EC) No 1831/2003 (amended)

Piperidine is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Piperidine 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: 03-11-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/13488

Piperidine: HSNO Approval: HSR001260 Approved with controls

Other Safety InformationIMAP assessments - Piperidine: Human health tier II assessment
DOT LabelCorrosive Flammable Liquid
Fire Hazards · 3 items

Piperidine evolves explosive concentrations of vapor at normal room temperatures. When heated to decomposition, it emits highly toxic fumes of nitrogen oxides. Dangerous, when exposed to heat, flame, or oxidizers. Avoid 1-Perchlorylpiperidine and oxidizing materials. Piperidine is a reactive compound and forms complexes with the salts of heavy metals. It evolves explosive concentrations of vapor at normal room temperatures. Keep away from igniting sources and heat. (EPA, 1998)

· Flammable/combustible material.

Highly flammable. Vapour/air mixtures are explosive.

Fire Potential · 2 items

This substance ... evolves explosive concentrations of vapor at normal room temperatures.

Dangerous /fire hazard/, when exposed to heat, flame or oxidizers.

Health Hazards · 2 items

Strong local irritant and may cause permanent injury after short exposure to small amounts. Ingestion may involve both irreversible and reversible changes. 30 to 60 mg/kg may cause symptoms in humans. (EPA, 1998)

· May cause toxic effects if inhaled or ingested.

Safety & protection

Fire Fighting · 2 items

Keep unnecesary people away; isolate hazard area and deny entry. Stay upwind; keep out of low area. Wear self-contained (positive pressure if available) breathing apparatus and full protective clothing. Isolate for 1/2 mile in all directions if tank car or truck is involved in fire.

Use water in large amounts, powder, alcohol-resistant foam, carbon dioxide. In case of fire: keep drums, etc., cool by spraying with water.

First Aid Measures · 4 items

Fresh air, rest. Half-upright position. Artificial respiration may be needed. Refer for medical attention.

Remove contaminated clothes. Rinse skin with plenty of water or shower. Refer for medical attention .

First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.

Rinse mouth. Do NOT induce vomiting. Give one or two glasses of water to drink. Refer for medical attention .

Accidental Release Measures · 2 items

· 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.

First Aid · 2 items

Warning: Piperidine is a basic irritant of skin and mucous membranes. May cause permanent injury after short exposure to small amounts.

General First Aid:

Safe StorageFireproof. Separated from strong oxidants, acids and incompatible materials. See Chemical Dangers.
Exposure Control and Personal Protection· Wear positive pressure self-contained breathing apparatus (SCBA).

Toxicology

Interactions · 1 item

A study in ddy mice successfully demonstrated that simultaneous administration of nitrite and piperidine led to a marked increase in the incidence of urinary bladder cancer when cholesterol pellets containing piperidine hydrochloride were surgically implanted into the urinary bladder and the rats were given sodium nitrite (0.1%) in their drinking water for 40 weeks. /Piperidine hydrochloride/

Ecotoxicity Values · 2 items

LC50 Daphnia magna /water flea/ 8.234 mg/L /48 hr. /Conditions of bioassay not specified/

LC50 Pimephales promelas (fathead minnow) 129.594 mg/L /96 hr. /Conditions of bioassay not specified/

Environmental Fate · 1 item

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), piperidine, which has a vapor pressure of 32.1 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase piperidine is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 4 hours(SRC), calculated from its rate constant of 8.9X10-11 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3).

Food Survey Values · 2 items

Piperidine concns in various West German foods and drink were; broken butterbeans 0.1 mg/kg, paprika 5.2 mg/kg, paprika with brine 5.6 mg/L, pepperoni 3.4 mg/kg, pepperoni with brine 0.4 mg/L, celery 1 mg/kg, celery with brine 0.1 mg/L, Bismarck herring 0.3 mg/kg, salted herring 0.7 mg/kg, smoked herring 0.2 mg/kg, Limburger cheese trace, coffee extract 2, freeze-dried coffee 2, freeze-dried coffee 1, defatted cocoa 9 mg/kg, barley 1 mg/kg, hops 2.5 mg/kg, and malt <0.1 mg/kg(1). Piperidine was also found in baked ham at 0.2 ppm(2) and 0.81 ppm(3), coffee at 1 ppm(2), fish sausage at 9 ppb(3) and as a volatile component of boiled beef(4).

Piperidine occurs at low levels in a variety of food products including baked ham (0.2 ppm), milk (0.11 ppm), coffee (1 ppm dry) and canned fish.

Adverse EffectsNeurotoxin - Other CNS neurotoxin
Exposure RoutesThe substance can be absorbed into the body by inhalation of its vapour, through the skin and by ingestion.

Regulatory information

FDA Requirements · 2 items

Piperidine is a food additive permitted for direct addition to food for human consumption as a synthetic flavoring substance and adjuvant in accordance with the following conditions: 1) the quantity added to food does not exceed the amount reasonably required to accomplish its intended physical, nutritive, or other technical effect in food, and 2) when intended for use in or on food it is of appropriate food grade and is prepared and handled as a food ingredient.

The following chemical has been specifically designated by the Administrator of the Drug Enforcement Administration as subject to the provisions of this part and parts 1309 and 1313 of this chapter. Piperidine and its salts are List 1 chemicals; DEA Code: 2704.

CERCLA Reportable Quantities · 1 item

Releases of CERCLA hazardous substances are subject to the release reporting requirement of CERCLA section 103, codified at 40 CFR part 302, in addition to the requirements of 40 CFR part 355. Piperidine is an extremely hazardous substance (EHS) subject to reporting requirements when stored in amounts in excess of its threshold planning quantity (TPQ) of 1,000 lbs.

DHS Chemicals of Interest (COI) · 4 items

Piperidine

1

10000

Flammable chemical that can be released at a facility.

Chemistry & industry

Pharmacology

Biological Half-LifeWhen injected iv into rats, piperidine disappeared exponentially with a half-life of 20 min.
Metabolism/Metabolites · 4 items

Mammals synthesize piperidine in the body, probably from the amino acid lysine. ... Mammals, including humans, excrete piperidine in urine in amounts of several mg/L under physiological conditions. Piperidine has been demonstrated to undergo oxidative metabolism in vitro in studies on rat liver microsomes. However, in the absence of quantitative data the importance of this metabolic route cannot be assessed.

Piperidine, a strong base, is excreted unchanged, & is normal constituent of urine probably arising from traces of cadaverine formed by intestinal micro-organisms.

In rats most of an ip dose of (3)H piperidine was excreted unchanged. Two major metabolites were identified as 3- and 4-hydroxypiperidine. Both compounds were also found in untreated animals and thus are probably metabolites of piperidine of exogenous or endogenous origin. These metabolites represent a detoxification mechanism, since they lack the potent pharmacological activities of the parent compound.

Metabolic studies of analgesics and anesthetics containing the piperidine ring have demonstrated the occurrence of N-hydroxylation, formation of a 6-oxo-derivative, and C-oxidative ring cleavage. N-nitrosopiperidine has been synthesized from piperidine and sodium nitrite in the gastric contents, isolated stomach and isolated small intestine of rats.

MeSH Pharmacological ClassificationA class of drugs that act by selective inhibition of calcium influx through cellular membranes.
Absorption, Distribution and Excretion · 4 items

... Piperidine is absorbed through the GI tract, through the skin and by inhalation.

It is well absorbed from gastrointestinal tract and absorption through skin is sufficient to produce death in small animals.

Mammals synthesize piperidine in the body, probably from the amino acid lysine. ... Mammals, including humans, excrete piperidine in urine in amounts of several mg/L under physiological conditions.

In hens, 35 to 70% of an injected dose is rapidly excreted unchanged in the urine. ... When injected iv into rats, piperidine disappeared exponentially with a half-life of 20 min. ... In rats most of an ip dose of (3)H piperidine was excreted unchanged.

Cellular LocationsCytoplasm

Uses & manufacturing

Uses · 6 items

Used as a chemical intermediate to produce drugs, wetting agents, and disinfectants; Also used as a rubber accelerator, a curing agent for epoxy resins, a flavoring agent, and an additive to oils and fuels; [HSDB]

Plastic Composites Manufacturing [Category: Industry]

Prepn of crystalline derivatives of aromatic nitro compd containing nuclear halogen atoms

Solvent and intermediate, curing agent for rubber and epoxy resins, catalyst for condensation reactions, ingredient in oils and fuels, complexing agent

Used in the manufacture of local anesthetics, analgesics and other pharmaceuticals, and for wetting agents and germicides.

INT FOR RUBBER VULCANIZATION ACCELERATORS; HARDENING AGENT FOR EPOXY RESINS

U.S. Imports · 2 items

(1975) 3.57X10+6 GRAMS (PRINCPL CUSTMS DISTS)

(1984) 5.00X10+5 g

U.S. Production · 6 items

2023: 2,500,000 - <4,000,000 lb

(1972) 2.17X10+8 GRAMS

(1975) 1.6X10+8 GRAMS

(1983) 2.75X10+8 g

Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#351]

This chemical is listed as a High Production Volume (HPV) (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and/or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B; 51FR21438).

Industry UsesIntermediate
Methods of Manufacturing · 3 items

May be obtained from piperine by heating with alcoholic potassium hydroxide, or from 1,5-diaminopentane hydrochloride by cyclization. Usually prepared by electrolytic reduction of pyridine.

Usually prepared by electrolytic reduction of pyridine.

Piperidine and most of its derivatives are easily produced by hydrogenation of the corresponding pyridine derivatives at elevated temperature and pressure over nickel, palladium, or ruthenium catalysts.

Formulations/PreparationsGrades: 95% and 98% pure

Related reactions

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