ChemicalBook > CAS DataBase List > Pyrrolidine

Pyrrolidine

Product Name
Pyrrolidine
CAS No.
123-75-1
Chemical Name
Pyrrolidine
Synonyms
Pyrrolidin;TETRAHYDROPYRROLE;PRL;PRD;Azolidine;Prolamine;FEMA 2523;FEMA 3523;AZACYCLOPENTANE;Tetrahydropyrrol
CBNumber
CB9852978
Molecular Formula
C4H9N
Formula Weight
71.12
MOL File
123-75-1.mol
More
Less

Pyrrolidine Property

Melting point:
-63 °C
Boiling point:
87-88 °C/760 mmHg (lit.)
Density 
0.852 g/mL at 25 °C (lit.)
vapor density 
2.45 (vs air)
vapor pressure 
128 mm Hg ( 39 °C)
refractive index 
n20/D 1.443(lit.)
FEMA 
3523 | PYRROLIDINE
Flash point:
37 °F
storage temp. 
Store below +30°C.
solubility 
water: miscible
form 
Liquid
pka
11.27(at 25℃)
color 
Colorless to Almost colorless
Odor
at 0.10 % in propylene glycol. ammoniacal animal egg amine
PH
12.9 (100g/l, H2O, 20℃)
explosive limit
1.6-10.6%(V)
Odor Type
ammoniacal
Water Solubility 
Miscible with alcohol, ether, chloroform and water.
Sensitive 
Air Sensitive
Merck 
14,8015
JECFA Number
1609
BRN 
102395
Dielectric constant
8.3000000000000007
Stability:
Stable; flammable. Incompatible with strong acids, strong oxidizing agents.
InChIKey
RWRDLPDLKQPQOW-UHFFFAOYSA-N
LogP
0.22 at 25℃
CAS DataBase Reference
123-75-1(CAS DataBase Reference)
NIST Chemistry Reference
Pyrrolidine(123-75-1)
EPA Substance Registry System
Pyrrolidine (123-75-1)
More
Less

Safety

Hazard Codes 
F,T,C
Risk Statements 
11-22-23-34-35-20/21/22-20/22-R35-R20/21/22-R11
Safety Statements 
16-26-36/37/39-45-33-S45-S36/37/39-S26-S16
RIDADR 
UN 1922 3/PG 2
WGK Germany 
2
RTECS 
UX9650000
F 
34
Autoignition Temperature
653 °F
TSCA 
Yes
HS Code 
2933 99 80
HazardClass 
3
PackingGroup 
II
Hazardous Substances Data
123-75-1(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: 433 mg/kg
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H225Highly Flammable liquid and vapour

H314Causes severe skin burns and eye damage

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
SAB1412061
Product name
ANTI-PRL antibody produced in mouse
Purity
clone 1A8, purified immunoglobulin, buffered aqueous solution
Packaging
100μg
Price
$524
Updated
2024/03/01
Sigma-Aldrich
Product number
8.07494
Product name
Pyrrolidine
Purity
for synthesis
Packaging
5ml
Price
$31.9
Updated
2024/03/01
Sigma-Aldrich
Product number
8.07494
Product name
Pyrrolidine
Purity
for synthesis
Packaging
1L
Price
$257
Updated
2024/03/01
Sigma-Aldrich
Product number
394238
Product name
Pyrrolidine
Purity
≥99.5%, purified by redistillation
Packaging
100ml
Price
$60.5
Updated
2024/03/01
Sigma-Aldrich
Product number
394238
Product name
Pyrrolidine
Purity
≥99.5%, purified by redistillation
Packaging
1l
Price
$258
Updated
2024/03/01
More
Less

Pyrrolidine Chemical Properties,Usage,Production

Chemical Properties

Pyrrolidine appears as a colorless to pale yellow liquid with an ammonia-like odor. It is infinitely miscible with water and conventional organic solvents such as methanol, acetone, ether, and chloroform. It acts as a lachrymator.
Chemically, pyrrolidine behaves like a secondary amine in every respect. For example, it undergoes Leuckart –Wallach and Mannich reactions and is readily converted into an enamine. In the presence of a catalyst, such as platinum at 360°C or rhodium at 650°C, pyrrole is formed. In the presence of a copper catalyst, N-methylpyrrolidone is converted into N-methylpyrrolidine.

Physical properties

Pyrrolidine has a penetrating amine-type odor, reminiscent of ammonia and piperidine. It is easy to turn yellow when exposed to light or humid air, easily soluble in water and ethanol. It is nauseating and diffusive.

Occurrence

Reported found in beer, bread, wheat bread, salmon caviar, fish, milk, leaves and stalks of celery, Camembert cheese, Limburger cheese, Russian cheeses, tilsit cheese, other cheeses, caviar, raw fatty fish, beer, Finnish whiskey, white wine, red wine, coffee, radish, malt, roasted peanut, sweet corn and roasted barley.

Uses

Pyrrolidine is a flammable alkaline liquid that undergoes reactions typical of secondary amines. It is used to prepare pesticides and rubber accelerators and as a chemical intermediate (usually the hydrochloride form) in the pharmaceutical industry. There is relatively limited industrial exposure to this material.

Application

Pyrrolidine is a heterocyclic compound used as a building block in the synthesis of wide range of pharmaceutical compounds, namely matrix metalloprotein inhibitors (MMPIs) and aminopeptidase N inhibitors (APNIs). It has been used for the synthesis of N-benzoyl pyrrolidine from benzaldehyde via oxidative amination. It may be used as a catalyst for the synthesis of N-sulfinyl aldimines from carbonyl compounds and sulfonamides.
Pyrrolidine can also be used to synthesize:
Taddol-pyrrolidine phosphoramidite, a ligand for rhodium-catalyzed [2+2+2] cycloaddition of pentenyl isocyanate and 4- ethynylanisole.
H,4 PyrrolidineQuin-BAM (′PBAM′), a selective catalyst for the aza-Henry addition of nitroalkanes to aryl aldimines.
1,2,3,3a,4,9-Hexahydropyrrolo[2,1-b]quinazoline by reacting with o-aminobenzaldehyde.

Definition

ChEBI: Pyrrolidine is a cyclic amine whose five-membered ring contains four carbon atoms and one nitrogen atom; the parent compound of the pyrrolidine family. It is a saturated organic heteromonocyclic parent, a member of pyrrolidines and an azacycloalkane. It is a conjugate base of a pyrrolidinium ion.

Preparation

Pyrrolidine is formed by reduction of pyrrole. Via overall 5-endo-trig cyclizations of homoallylic tosylamides. Pyrrolidine can be produced from butanediol and ammonia, e.g., over an aluminum thorium oxide catalyst at 300°C or over a nickel catalyst at 200°C and 20 MPa under hydrogenation conditions. It can also be produced from THF and ammonia over aluminum oxide at 275-375°C.

Aroma threshold values

Detection: 20.2 ppm

Taste threshold values

Taste characteristics at 50 ppm: ammonia and fishy, amine-like with seaweed and shellfish nuances.

General Description

Pyrrolidine is a saturated heterocycliccompound having one nitrogenatom in a five-membered ring. It is a colorless to pale yellow liquid with an ammonia-like odor. It is found in certain plants andthe ring structure is present in manyalkaloids. Flash point 37°F. Density 0.85 g / cm3. Vapors heavier than air. Produces toxic oxides of nitrogen during combustion.

Air & Water Reactions

Highly flammable. Very soluble in water.

Reactivity Profile

Tetrahydro pyrrole 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. May generate hydrogen, a flammable gas, in combination with strong reducing agents such as hydrides. An explosion occurred when a mixture of Tetrahydro pyrrole, benzaldehyde, and propionic acid was heated in an attempt to form porphyrins.

Hazard

Flammable, dangerous fire risk. Toxic by ingestion and inhalation.

Health Hazard

The acute toxicity of pyrrolidine is moderateon test animals. It is somewhat less toxicthan pyrrole. The vapors are an irritant tothe eyes and respiratory tract. The liquid iscorrosive to the skin. Contact with the eyescan cause damage. The oral LD50 value inrats is 300 mg/kg, while the inhalation LC50value in mice is 1300 mg/m3/2 h (NIOSH1986).

Fire Hazard

Flammable/combustible material. May be ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.

Flammability and Explosibility

Highly flammable

Safety Profile

Poison by ingestion and intravenous routes. Moderately toxic by inhalation. Dangerous fire hazard when exposed to heat or flame; can react vigorously with oxidizing materials. To fight fire, use alcohol foam, CO2, dry chemical. When heated to decomposition it emits hghly toxic fumes of NOx.

Purification Methods

Dry pyrrolidine with BaO or sodium, then fractionally distil it, under N2, through a Todd column (p 11) packed with glass helices. [Beilstein 20 H 159, 20 I 36, 20 II 79, 20 III/IV 2072, 20/1 V 162.]

Pyrrolidine Preparation Products And Raw materials

Raw materials

Preparation Products

Ramipril METHYL 3-((PYRROLIDIN-1-YL)METHYL)BENZOATE ETHYL 3,5-DIMETHYLISOXAZOLE-4-CARBOXYLATE Barnidipine hydrochloride 4,5,6,7-TETRAHYDRO-2-METHYLFURO[3,2-C]PYRIDINE 6-Bromoindole-3-carboxaldehyde Alizapride 6-Benzyloxyindole Rocuronium bromide 6-(1-PYRROLIDINYL)-3-PYRIDINAMINE 6-Methoxyindole Gestrinone 6-Fluorotryptamine hydrochloride N-[2-(4-Bromophenoxy)ethyl]pyrrolidine Bis(pinacolato)diboron [6-(1-PYRROLIDINYL)-3-PYRIDINYL]METHANOL 6-Methoxy-1H-indole-3-carbaldehyde TOSUFLOXACIN TOSILATE BEPRIDIL 3-Methyl-4-isoxazolecarboxylic acid 3,5-DIMETHYLISOXAZOLE-4-CARBONYL CHLORIDE 4-PYRROLIDINOBUTYLAMINE 5-NITRO-2-(1-PYRROLIDINYL)PYRIDINE 5-BROMO-2-(PYRROLIDIN-1-YL)PYRIDINE 6-(1-PYRROLIDINYL)NICOTINALDEHYDE Methyl 1-Methyl-2-oxopyrrolidine-3-carboxylate 1-(2-Aminoethyl)pyrrolidine 4-(1-Pyrrolidinyl)piperidine (2-PYRROLIDIN-1-YL-ETHYL)-HYDRAZINE 1-BENZYL-3-METHYL-4-PIPERIDONE 5-BROMO-2-(PYRROLIDIN-1-YL)PYRIMIDINE Sultopride hydrochloride PYRROLIDIN-1-YL-ACETIC ACID 1-(4-AMINO-2,6-DICHLOROPHENOXY)-3-(PYRROLIDIN-1-YL)PROPAN-2-OL 3,5-DIMETHYLISOXAZOLE-4-CARBOXYLIC ACID PYRROLIDINE-1-SULFONYL CHLORIDE 1-(2-Chloroethyl)pyrrolidine Hydrochloride 1-(3-PYRROLIDINOPROPYL)PIPERAZINE Indole-6-carboxylic acid Simvastatin
More
Less

Pyrrolidine Suppliers

Americas 1 Australia 1 Austria 1 Belgium 4 Canada 3 China 408 China Hong Kong 1 Czech 1 Europe 4 France 3 Germany 18 India 56 Italy 1 Japan 10 Poland 1 Slovakia 1 South Korea 1 Switzerland 3 The Netherlands 1 Ukraine 1 United Kingdom 17 United States 74 Global 611
GLR Innovations
Tel
+91 9891111994
Email
info@glrgroup.in
Country
India
ProdList
4535
Advantage
58
TCI Chemicals (India) Pvt. Ltd.
Tel
--
Fax
--
Email
sales-in@tcichemicals.com
Country
India
ProdList
6768
Advantage
58
Jigs chemical
Tel
--
Fax
--
Email
info@jigschemical.com
Country
India
ProdList
318
Advantage
58
Sisco Research Laboratories Pvt. Ltd.
Tel
--
Fax
--
Email
marketing@srlchem.com
Country
India
ProdList
4315
Advantage
58
Triveni chemicals
Tel
--
Fax
--
Email
sales@trivenichemical.com
Country
India
ProdList
6088
Advantage
58
Trignokem International.
Tel
--
Fax
--
Email
ignokem@gmail.com
Country
India
ProdList
233
Advantage
58
Multichem Specialities Private Limited.
Tel
--
Fax
--
Email
sales@multichemindia.com
Country
India
ProdList
127
Advantage
58
Perfect Chemical
Tel
--
Fax
--
Country
India
ProdList
171
Advantage
58
Shivam Pharma Chemicals
Tel
--
Fax
--
Email
info@shivampharma.com
Country
India
ProdList
656
Advantage
58
J. N. Chemical
Tel
--
Fax
--
Email
info@jnchemicals.com
Country
India
ProdList
139
Advantage
58
Sudarshan Pharma Industries Limited.
Tel
--
Fax
--
Email
@sudarshangrp.com
Country
India
ProdList
157
Advantage
58
Sachin Chemicals
Tel
--
Fax
--
Email
sachinchemicals@gmail.com
Country
India
ProdList
140
Advantage
58
Azole Rasayanas India Private Limited
Tel
--
Fax
--
Email
info@azolerasayanas.com
Country
India
ProdList
681
Advantage
58
A. B. Enterprises
Tel
--
Fax
--
Country
India
ProdList
226
Advantage
58
Jay Chem Marketing
Tel
--
Fax
--
Country
India
ProdList
231
Advantage
58
Paras Chemical Industries
Tel
--
Fax
--
Email
info@paraschemicals.com
Country
India
ProdList
54
Advantage
58
Leo Chemo Plast Pvt Ltd
Tel
--
Fax
--
Country
India
ProdList
39
Advantage
58
BASF India Limited
Tel
--
Fax
--
Country
India
ProdList
138
Advantage
58
Molychem
Tel
--
Fax
--
Country
India
ProdList
576
Advantage
58
Lok Chemicals Pvt., Ltd.
Tel
--
Fax
--
Email
nidhi@lokchem.com
Country
India
ProdList
123
Advantage
58
ASM Organics
Tel
--
Fax
--
Country
India
ProdList
1185
Advantage
58
Renuka Interchem
Tel
--
Fax
--
Country
India
ProdList
116
Advantage
58
Antares Chem Private Limited
Tel
--
Fax
--
Country
India
ProdList
179
Advantage
58
Manav Bio -Chem Impex Pvt Ltd
Tel
--
Fax
--
Email
cheminquiry@gmail.com
Country
India
ProdList
204
Advantage
58
Deep Prabha Transchem
Tel
--
Fax
--
Email
dipen@deepprabha.com
Country
India
ProdList
108
Advantage
58
Associated Agencies
Tel
--
Fax
--
Email
info@assoagen.com
Country
India
ProdList
29
Advantage
58
Saradhi Organics
Tel
--
Fax
--
Email
sales@saradhiorganics.com
Country
India
ProdList
183
Advantage
58
Oceanic Pharmachem Pvt., Ltd. (OPPL)
Tel
--
Fax
--
Email
info@oceanicpharmachem.com
Country
India
ProdList
946
Advantage
58
Innovative Synthetic Molecules
Tel
--
Fax
--
Country
India
ProdList
526
Advantage
58
Base Chemicals India Company
Tel
--
Fax
--
Country
India
ProdList
151
Advantage
58
Dishman Pharmaceuticals & Chemicals Ltd
Tel
--
Fax
--
Country
India
ProdList
74
Advantage
58
Mesha Pharma Private Limited
Tel
--
Fax
--
Country
India
ProdList
133
Advantage
58
Loba Chemie Pvt Ltd
Tel
--
Fax
--
Country
India
ProdList
498
Advantage
58
Dr. Silviu Pharmachem Pvt., Ltd. (DRSPL)
Tel
--
Fax
--
Email
info@drspl.in
Country
India
ProdList
143
Advantage
58
Panax-Matrix Research Laboratory
Tel
--
Fax
--
Country
India
ProdList
3
Advantage
58
Sanjay Chemicals (India) Pvt., Ltd.
Tel
--
Fax
--
Email
abdul@sanjaychemindia.com
Country
India
ProdList
159
Advantage
58
Meru Chem Pvt. Ltd.
Tel
--
Fax
--
Email
meruchempltd@gmail.com
Country
India
ProdList
174
Advantage
58
Molecraft LifeSciences Pvt Ltd
Tel
--
Fax
--
Email
info@molecraft.com
Country
India
ProdList
757
Advantage
0
Anand Agencies
Tel
--
Fax
--
Email
en@gmail.com
Country
India
ProdList
2332
Advantage
58
Avra Synthesis Pvt Ltd
Tel
--
Fax
--
Email
info@avrasynthesis.com
Country
India
ProdList
1603
Advantage
30
Ganesh Chem tech Pvt Ltd
Tel
--
Fax
--
Country
India
ProdList
44
Advantage
58
Brisben Chemicals
Tel
--
Fax
--
Country
India
ProdList
508
Advantage
58
Trilok Enterprises
Tel
--
Fax
--
Country
India
ProdList
25
Advantage
58
Mahavir Interchem
Tel
--
Fax
--
Country
India
ProdList
33
Advantage
58
Vcare Medicines
Tel
--
Fax
--
Country
India
ProdList
114
Advantage
58
Manav Biochem Impex Private Limited
Tel
--
Fax
--
Country
India
ProdList
198
Advantage
58
Central Drug House(P) Ltd.
Tel
--
Fax
--
Email
sales@cdhfinechemical.com
Country
India
ProdList
6157
Advantage
58
LOBA CHEMIE PVT.LTD.
Tel
--
Fax
--
Email
info@lobachemie.com
Country
India
ProdList
3075
Advantage
58
Dr Prem's Molecules Pvt. Ltd.
Tel
--
Fax
--
Email
prem@dpmolecules.com
Country
India
ProdList
544
Advantage
50
More
Less

View Lastest Price from Pyrrolidine manufacturers

Dorne Chemical Technology co. LTD
Product
Pyrrolidine 123-75-1
Price
US $10.00/ASSAYS
Min. Order
1ASSAYS
Purity
99%
Supply Ability
10 tons
Release date
2021-04-10
Hebei Weibang Biotechnology Co., Ltd
Product
Pyrrolidine 123-75-1
Price
US $100.00/Kg/Drum
Min. Order
1Kg/Drum
Purity
99%min
Supply Ability
200TON
Release date
2024-10-28
Hebei Dangtong Import and export Co LTD
Product
Pyrrolidine 123-75-1
Price
US $60.00-55.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20Tons
Release date
2023-10-10

123-75-1, PyrrolidineRelated Search:

Pyrrole Tellurium tetrachloride Tetrahydropyran Tetrahydro-4H-pyran-4-one Tetrahydrofuran Tetrahydro-2H-pyran-4-carbonyl chloride Tetrahydro-4-pyranol Methyl tetrahydropyran-4-carboxylate Tetrahydro-2H-pyran-4-carboxylic acid Tetrahydro-4H-Pyran-4-one Ethyl Tetrahydropyran-4-Carboxylate 1-AMINOPYRROLIDINE 1-Methyl-3-pyrrolidinol 3-CARBAMOYL-PROXYL 1-Cyanopyrrolidine 1-FORMYLPYRROLIDINE 1-Methylpyrrolidine 1-(TRIMETHYLSILYL)PYRROLIDINE

  • TETRAMETHYLENEIMINE
  • pyrrolidine,tetrahydropyrrole
  • PYRROLIDINE,REAGENT
  • TETRAHYDROPYRROLE(PYRROLIDINE)
  • PYRROLIDINE 99+%
  • PYRROLIDINE, REDISTILLED, 99.5+%
  • 1-AZACYCLOPENTANE
  • AKOS BBS-00003603
  • TETRAHYDROPYRROLE
  • PYRROLIDINE
  • PRL
  • PRD
  • Tetrahydropyrrole, 1-Azacyclopentane
  • Pyrrolidine, 99+% 250ML
  • NSC 62781
  • PYRROLIDINE extrapure AR
  • Tetrahydropyrrole, Tetramethyleneimine
  • Pyrrolidine ,97%
  • Tetrahydro-1H-pyrrole
  • Pyrrolidine,Tetrahydropyrrole, Tetramethyleneimine
  • Pyrrolidine, 99.5+%, purified by redistillation, AcroSeal
  • PYRROLIDINE FOR SYNTHESIS 250 ML
  • PYRROLIDINE FOR SYNTHESIS 5 ML
  • PYRROLIDINE FOR SYNTHESIS 1 L
  • Pyrrolidine >=99.5%, purified by redistillation
  • Pyrrolidine puriss. p.a., >=99.0%
  • Four hydrogen pyrrole
  • Luterotropic hormone
  • Lutetropin
  • Prolactin from rat
  • Lactotrophin
  • Mamotrophin
  • Prolactin from mouse
  • Azolidine
  • Butylenimine
  • perhydroazole
  • Perhydropyrrole
  • Prolamine
  • Pyrrole, tetrahydro-
  • Pyrrolidene
  • Pyrrolidin
  • pyrrolidinering
  • tetrahydroazole
  • Tetrahydro pyrrole manufacturer
  • Pyrrolidine China supplier
  • PYRROLIDINE, 99%PYRROLIDINE, 99%PYRROLIDINE, 99%PYRROLIDINE, 99%
  • Tetrahydropyrrol
  • tetrahydro-pyrrol
  • Tetramethylenimin
  • Tetramethylenimine
  • LABOTEST-BB LTBB000397
  • AZACYCLOPENTANE
  • FEMA 2523
  • FEMA 3523
  • Pyrrolidine liquid
  • Pyrrolidine&gt
  • cas 123-75-1 Pyrrolidine
  • Human PRL Protein, His Tag