1-(2-Aminoethyl)piperazine(AEP) - ≥99% , CAS No.140-31-8

CAS: 140-31-8 Cat. No.: A101279 Peso molecular: 129.2 Beilstein Registry Number: 104363 Número EC: 205-411-0
Disponible para pedir
GRADE & PURITY ≥99%
Synonyms
AI3-52274 | 1-(2-Aminoethyl)piperazine | 1-(2-aminoethyl)-piperazine | 2-(piperazin-1-yl)ethan-1-amine | n-(2-aminoethyl) piperazine | 2-aminoethylpiperazine | CCRIS 6678 | NSC 38968 | 2-(piperazin-1-yl)ethanamine | Piperazine, 1-(2-aminoethyl)- | Z571278
Storage
Room temperature,Argon charged,Cool
Shipped In
FedEx DG Service
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25ml
A101279-25ml
3
9,90US$
100ml
A101279-100ml
3
13,90US$
500ml
A101279-500ml
3
45,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Argon charged,Cool Ships FedEx DG Service Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 67 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

1-(2-Aminoethyl)piperazine is utilized in a variety of reactions. Its is used for studying corrosion inhibition, biological activity, and metal ligand effects on catalysis
Used for studying corrosion inhibition

Specifications

Sinónimos
AI3-52274 | 1-(2-Aminoethyl)piperazine | 1-(2-aminoethyl)-piperazine | 2-(piperazin-1-yl)ethan-1-amine | n-(2-aminoethyl) piperazine | 2-aminoethylpiperazine | CCRIS 6678 | NSC 38968 | 2-(piperazin-1-yl)ethanamine | Piperazine, 1-(2-aminoethyl)- | Z571278
Especificaciones y pureza
≥99%
Condiciones de almacenamiento de almacenamiento
Room temperature, Argon charged, Cool
Enviado en
FedEx DG Service
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥99%
Nombres e identificadores
Pubchem Sid504751736
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504751736
Sonrisas canónicasC1CN(CCN1)CCN
IUPAC Name2-piperazin-1-ylethanamine
InChIKeyIMUDHTPIFIBORV-UHFFFAOYSA-N
INCHI1S/C6H15N3/c7-1-4-9-5-2-8-3-6-9/h8H,1-7H2
Isómeros SMILES C1CN(CCN1)CCN
WGK Alemania 2
RTECS TK8050000
Número ONU 2815
Grupo de embalaje III
Peso molecular 129.2
Beilstein 104363
Reaxy-Rn 104363
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=104363&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseDiazinanes
SubclassPiperazines
Intermediate Tree Nodes Not available
Direct ParentN-alkylpiperazines
Alternative Parents Trialkylamines  Dialkylamines  Azacyclic compounds  Organopnictogen compounds  Monoalkylamines  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents N-alkylpiperazine - Tertiary aliphatic amine - Tertiary amine - Azacycle - Secondary amine - Secondary aliphatic amine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Primary aliphatic amine - Amine - Aliphatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as n-alkylpiperazines. These are organic compounds containing a piperazine ring where the nitrogen ring atom carries an alkyl group.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA3 Tclin Carbonic anhydrase III (753 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA6 Tclin Carbonic anhydrase VI (993 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA1 Tclin Carbonic anhydrase I (13240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5B Tclin Carbonic anhydrase VB (957 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5A Tclin Carbonic anhydrase VA (1168 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA14 Tclin Carbonic anhydrase XIV (1305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA12 Tclin Carbonic anhydrase XII (6231 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA9 Tclin Carbonic anhydrase IX (8255 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Ca7 Carbonic anhydrase VII (3 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ca13 Carbonic anhydrase XIII (322 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA4 Carbonic anhydrase IV (1713 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Carbonic anhydrase (69 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ca15 Carbonic anhydrase 15 (173 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CAN2 Carbonic anhydrase 2 (140 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

39 results found

Lot NumberCertificate TypeFechaArticulo
F2609249Certificate of AnalysisJun 13, 2026 A101279
F2609278Certificate of AnalysisJun 12, 2026 A101279
F2609253Certificate of AnalysisJun 12, 2026 A101279
F2609252Certificate of AnalysisJun 12, 2026 A101279
F2609251Certificate of AnalysisJun 12, 2026 A101279
F2609250Certificate of AnalysisJun 12, 2026 A101279
F2609248Certificate of AnalysisJun 12, 2026 A101279
F2609247Certificate of AnalysisJun 12, 2026 A101279
E2618202Certificate of AnalysisMay 27, 2026 A101279
E2618203Certificate of AnalysisMay 27, 2026 A101279
E2618204Certificate of AnalysisMay 27, 2026 A101279
F2609254Certificate of AnalysisMay 21, 2026 A101279
F2609255Certificate of AnalysisMay 21, 2026 A101279
D2608461Certificate of AnalysisApr 03, 2026 A101279
D2608462Certificate of AnalysisApr 03, 2026 A101279
D2603027Certificate of AnalysisMar 31, 2026 A101279
D2603026Certificate of AnalysisMar 31, 2026 A101279
L2525126Certificate of AnalysisJan 04, 2026 A101279
A2607001Certificate of AnalysisJan 04, 2026 A101279
L2517004Certificate of AnalysisJul 30, 2025 A101279
G2521006Certificate of AnalysisJul 30, 2025 A101279
A2107083Certificate of AnalysisOct 08, 2024 A101279
A2107082Certificate of AnalysisOct 08, 2024 A101279
A2107081Certificate of AnalysisOct 08, 2024 A101279
G2405138Certificate of AnalysisMar 23, 2024 A101279
H2303051Certificate of AnalysisAug 05, 2023 A101279
G1908016Certificate of AnalysisApr 17, 2023 A101279
G2227573Certificate of AnalysisJul 15, 2022 A101279
J2522096Certificate of AnalysisJul 15, 2022 A101279
J2425143Certificate of AnalysisJul 15, 2022 A101279
H2303074Certificate of AnalysisJul 15, 2022 A101279
G2306233Certificate of AnalysisJul 15, 2022 A101279
G2227574Certificate of AnalysisJul 15, 2022 A101279
D2524048Certificate of AnalysisJul 15, 2022 A101279
G2227572Certificate of AnalysisJul 15, 2022 A101279
G2227571Certificate of AnalysisJul 15, 2022 A101279
B2512060Certificate of AnalysisJul 15, 2022 A101279
C2525145Certificate of AnalysisJul 15, 2022 A101279
G1813083Certificate of AnalysisMay 09, 2022 A101279

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Propiedades químicas y físicas
SolubilidadSoluble in water.
SensibilidadAir sensitive
Índice de refracción1.499-1.501
Punto de inflamación (°F)197.6 °F
Punto de inflamación (°C) 88 ℃
Punto de ebullición (°C)218-222°C
Punto de fusión (°C)-19°C
Peso molecular129.199 g/mol
XLogP3-1.300
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Exact Mass129.127 Da
Monoisotopic Mass129.127 Da
Topological Polar Surface Area41.300 Ų
Heavy Atom Count9
Formal Charge0
Complexity68.700
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
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