Cas no 934-98-5 (2-(4-methylpiperazin-1-yl)ethan-1-amine)

2-(4-methylpiperazin-1-yl)ethan-1-amine structure
934-98-5 structure
Product Name:2-(4-methylpiperazin-1-yl)ethan-1-amine
CAS No:934-98-5
MF:C7H17N3
MW:143.229981184006
MDL:MFCD03701701
CID:40329
PubChem ID:70284
Update Time:2024-10-26

2-(4-methylpiperazin-1-yl)ethan-1-amine Chemical and Physical Properties

Names and Identifiers

    • 2-(4-Methylpiperazin-1-yl)ethylamine
    • 1-(2-Aminoethyl)-4-methylpiperazine
    • 1-(2-Aminoethyl)-4-Methyl-Piperazine
    • 2-(4-Methylpiperazin-1-yl)ethanamine
    • 2-(4-Methyl-piperazin-1-yl)-ethylamine
    • 4-Methyl-1-piperazineethanamine
    • 1-Piperazineethanamine,4-methyl
    • 4-Methyl-1-piperazineethanamine (ACI)
    • Piperazine, 1-(2-aminoethyl)-4-methyl- (6CI, 7CI, 8CI)
    • 1-Methyl-4-(2-aminoethyl)piperazine
    • 2-(4-Methyl-1-piperazinyl)ethanamine
    • 2-(4-Methylpiperazin-1-yl)ethan-1-amine
    • 2-(4-Methylpiperazino)ethanamine
    • 4-(2-Aminoethyl)-1-methylpiperazine
    • CS-W007512
    • ALBB-005818
    • STK500900
    • 2-(4-methylpiperazin-1-yl)-ethanamine
    • 2-(4-Methyl-1-piperazino)ethylamine Hydrochloride
    • Q27157656
    • 2-(4-methylpiperazin-1-yl) ethylamine
    • DTXSID10239420
    • 2-(4-methyl-piperazine-1-yl)-ethyl amine
    • NS00039568
    • 2-(4-methylpiperazin-1-yl)-ethylamine
    • CHEBI:84290
    • 2(4-methylpiperazin-1-yl)ethylamine
    • AB15815
    • DB-019466
    • Piperazine 1-[2-aminoethyl]-4-methyl-
    • SCHEMBL42017
    • Z79BOY08I2
    • EINECS 213-296-3
    • SCHEMBL4480122
    • 4-Methylpiperazine-1-ethylamine
    • EN300-24106
    • 2-(4-Methyl-piperazin-1-yl)-ethylamine, AldrichCPR
    • A846010
    • MFCD03701701
    • UNII-Z79BOY08I2
    • CCG-358157
    • 2-(4-Methyl-1-piperazinyl)ethanamine #
    • A2398
    • 2-(4-METHYL-1-PIPERAZINYL)ETHYLAMINE
    • DTXCID30161911
    • F2187-2164
    • AKOS000201108
    • 1-(2-aminoethyl)-4-methyl piperazine
    • Piperazine, 1-(2-aminoethyl)-4-methyl-
    • SY032261
    • Piperazine 1-(2-aminoethyl)-4-methyl-
    • LF-0565
    • J-506071
    • 1-Piperazineethanamine, 4-methyl-
    • 934-98-5
    • 2-(4-methylpiperazin-1-yl)ethan-1-amine
    • MDL: MFCD03701701
    • Inchi: 1S/C7H17N3/c1-9-4-6-10(3-2-8)7-5-9/h2-8H2,1H3
    • InChI Key: GOWUDHPKGOIDIX-UHFFFAOYSA-N
    • SMILES: NCCN1CCN(C)CC1

Computed Properties

  • Exact Mass: 143.14200
  • Monoisotopic Mass: 143.142
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 2
  • Complexity: 86.9
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: -0.9
  • Topological Polar Surface Area: 32.5A^2

Experimental Properties

  • Density: 0.956
  • Boiling Point: 215.4℃ at 760 mmHg
  • Flash Point: 83.3 °C
  • Refractive Index: 1.487
  • PSA: 32.50000
  • LogP: -0.23140
  • Sensitiveness: Air Sensitive

2-(4-methylpiperazin-1-yl)ethan-1-amine Security Information

  • Hazard Statement: Irritant
  • Hazardous Material transportation number:2735
  • Hazard Category Code: 36/37/38-22
  • Safety Instruction: S26-S36/37/39
  • Hazardous Material Identification: Xi
  • Risk Phrases:R36/37/38
  • HazardClass:8
  • PackingGroup:

2-(4-methylpiperazin-1-yl)ethan-1-amine Customs Data

  • HS CODE:2933599090
  • Customs Data:

    China Customs Code:

    2933599090

    Overview:

    2933599090. Other compounds with pyrimidine ring in structure(Including other compounds with piperazine ring on the structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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2-(4-methylpiperazin-1-yl)ethan-1-amine Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Hydrochloric acid Solvents: Methanol ,  1,4-Dioxane ;  1 h, rt
Reference
Synthesis and evaluation of chirally defined side chain variants of 7-chloro-4-aminoquinoline to overcome drug resistance in malaria chemotherapy
Dola, Vasantha Rao; Soni, Awakash; Agarwal, Pooja; Ahmad, Hafsa; Raju, Kanumuri Siva Rama; et al, Antimicrobial Agents and Chemotherapy, 2017, 61(3),

Production Method 2

Reaction Conditions
1.1 Reagents: Lithium aluminum hydride Solvents: Tetrahydrofuran ;  0 °C; 1 h, rt; cooled
1.2 Reagents: Sodium hydroxide Solvents: Water ;  20 min, cooled
Reference
Phenyl-urea and phenyl-carbamate derivatives as inhibitors of protein aggregation
, World Intellectual Property Organization, , ,

Production Method 3

Reaction Conditions
1.1 Reagents: Lithium aluminum hydride Solvents: Diethyl ether ,  Tetrahydrofuran ;  0 °C; 24 h, rt; cooled
1.2 Reagents: Sodium hydroxide Solvents: Water ;  20 min, cooled
Reference
2,3-Dihydro-2-oxo-1H-benzimidazole-1-carboxamides with Selective Affinity for the 5-HT4 Receptor: Synthesis and Structure-Affinity and Structure-Activity Relationships of a New Series of Partial Agonist and Antagonist Derivatives
Tapia, Ines; Alonso-Cires, Luisa; Lopez-Tudanca, Pedro Luis; Mosquera, Ramon; Labeaga, Luis; et al, Journal of Medicinal Chemistry, 1999, 42(15), 2870-2880

Production Method 4

Reaction Conditions
1.1 Solvents: Diethyl ether
Reference
Guanidines having antihypertensive activity. I. Dialkylaminoalkylamino-2-imidazolines
Najer, Henry; Giudicelli, Rene; Sette, Jacques, Bulletin de la Societe Chimique de France, 1962, 556, 556-9

Production Method 5

Reaction Conditions
1.1 Reagents: Lithium aluminum hydride Solvents: Diethyl ether ,  Tetrahydrofuran ;  0 °C; 1 h, 0 °C; 0 °C → rt; overnight, rt
1.2 Reagents: Sodium hydroxide Solvents: Water ;  20 min, rt
Reference
New derivatives of quinoline-4-carboxylic acid with antiplasmodial activity
Hochegger, Patrick ; Faist, Johanna; Seebacher, Werner; Saf, Robert; Maeser, Pascal; et al, Bioorganic & Medicinal Chemistry, 2017, 25(7), 2251-2259

Production Method 6

Reaction Conditions
1.1 Reagents: Hydrazine Solvents: Ethanol ;  24 h, reflux
Reference
Structural optimizations and bioevaluation of N-substituted acridone derivatives as strong topoisomerase II inhibitors
Li, Zhi-Ying; Xu, Guang-Sen; Song, Yu-Liang; Li, Xun, Bioorganic Chemistry, 2022, 119,

Production Method 7

Reaction Conditions
1.1 Reagents: Hydrochloric acid Solvents: 1,4-Dioxane ;  1 h, 27 °C; 10 min, 27 °C
1.2 Reagents: Triethylamine ,  Hydrochloric acid Solvents: Water ;  basified
Reference
Preparation of aminoquinoline derivatives for use as antimalarials
, India, , ,

Production Method 8

Reaction Conditions
1.1 Reagents: Lithium aluminum hydride Solvents: Diethyl ether
Reference
Synthesis and cytotoxicity of novel indirubin-5-carboxamides
Cheng, Xinlai; Rasque, Paul; Vatter, Sandra; Merz, Karl-Heinz; Eisenbrand, Gerhard, Bioorganic & Medicinal Chemistry, 2010, 18(12), 4509-4515

Production Method 9

Reaction Conditions
1.1 Reagents: Hydrazine hydrate (1:1) Solvents: Ethanol ;  24 h, reflux
Reference
New pyrido[3,4-g]quinazoline derivatives as CLK1 and DYRK1A inhibitors: synthesis, biological evaluation and binding mode analysis
Tazarki, Helmi ; Zeinyeh, Wael; Esvan, Yannick J.; Knapp, Stefan; Chatterjee, Deep; et al, European Journal of Medicinal Chemistry, 2019, 166, 304-317

Production Method 10

Reaction Conditions
1.1 Reagents: Hydrazine hydrate (1:1) Solvents: Ethanol ;  4 - 6 h, reflux
Reference
Synthesis and antitumor activity of 5-bromo-7-azaindolin-2-one derivatives containing a 2,4-dimethyl-1H-pyrrole-3-carboxamide moiety
Zhang, Jun; Shen, Weiyi; Li, Xiaoning; Chai, Yun; Li, Senjun; et al, Molecules, 2016, 21(12), 1674-1683

Production Method 11

Reaction Conditions
1.1 Reagents: Hydrazine hydrate (1:1) Solvents: Ethanol ;  24 h, rt → reflux
Reference
Drug containing cinnamic acid amide, especially for chronic pain treatment
, Japan, , ,

Production Method 12

Reaction Conditions
1.1 Reagents: Hydrazine hydrate (1:1) Solvents: Ethanol ;  rt; 24 h, reflux
Reference
Preparation of cinnamic acid amide derivatives as analgesics
, World Intellectual Property Organization, , ,

2-(4-methylpiperazin-1-yl)ethan-1-amine Raw materials

2-(4-methylpiperazin-1-yl)ethan-1-amine Preparation Products

2-(4-methylpiperazin-1-yl)ethan-1-amine Suppliers

Suzhou Senfeida Chemical Co., Ltd
Gold Member
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(CAS:934-98-5)4-Methyl-1-piperazin
Order Number:1619449
Stock Status:in Stock
Quantity:Company Customization
Purity:98%
Pricing Information Last Updated:Monday, 14 April 2025 21:49
Price ($):discuss personally
Amadis Chemical Company Limited
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(CAS:934-98-5)2-(4-methylpiperazin-1-yl)ethan-1-amine
Order Number:A844616
Stock Status:in Stock
Quantity:5g/25g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 07:03
Price ($):219.0/877.0
Tiancheng Chemical (Jiangsu) Co., Ltd
Gold Member
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(CAS:934-98-5)4-甲基-1-哌嗪乙胺
Order Number:LE1619449
Stock Status:in Stock
Quantity:25KG,200KG,1000KG
Purity:99%
Pricing Information Last Updated:Friday, 20 June 2025 12:29
Price ($):discuss personally
Recommended suppliers
Suzhou Senfeida Chemical Co., Ltd
(CAS:934-98-5)4-Methyl-1-piperazin
1619449
Purity:98%
Quantity:Company Customization
Price ($):Inquiry
Email
Amadis Chemical Company Limited
(CAS:934-98-5)2-(4-methylpiperazin-1-yl)ethan-1-amine
A844616
Purity:99%/99%
Quantity:5g/25g
Price ($):219.0/877.0
Email