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2-Methoxy-2-methylpropan-1-amine

Base Information
  • Chemical Name:2-Methoxy-2-methylpropan-1-amine
  • CAS No.:89282-70-2
  • Molecular Formula:C5H13 N O
  • Molecular Weight:103.164
  • Hs Code.:2922199090
  • European Community (EC) Number:804-308-3
  • DSSTox Substance ID:DTXSID80472701
  • Wikidata:Q82301775
  • Mol file:89282-70-2.mol
2-Methoxy-2-methylpropan-1-amine

Synonyms:2-methoxy-2-methylpropan-1-amine;89282-70-2;2-Methoxy-2-methylpropylamine;2-METHOXY-2-METHYL-PROPYLAMINE;2-methoxyisobutylamine;(2-methoxy-2-methylpropyl)amine;MFCD01821229;2-methoxy-2-methyl-propan-1-amine;1-Propanamine, 2-methoxy-2-methyl-;2-methoxy-2-methyl-1-propanamine hcl;SCHEMBL456975;DTXSID80472701;ZSTYQALWKOGXOV-UHFFFAOYSA-N;AMY36536;AKOS005172310;GS-4548;2-methoxy-2-methyl-propylamine, AldrichCPR;BB 0261960;FT-0646671;FT-0655914;D87550;EN300-103952;J-509781

Suppliers and Price of 2-Methoxy-2-methylpropan-1-amine
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Abosyn
  • 2-methoxy-2-methylpropan-1-amine 95+%
  • 1g
  • $ 135.00
  • Acrotein
  • 2-Methoxy-2-methyl-1-propanamineHCl 97%
  • 1g
  • $ 161.52
  • Acrotein
  • 2-Methoxy-2-methyl-1-propanamineHCl 97%
  • 0.5g
  • $ 100.83
  • Activate Scientific
  • 2-Methoxy-2-methylpropan-1-amine 95+%
  • 1 g
  • $ 165.00
  • Activate Scientific
  • 2-Methoxy-2-methylpropan-1-amine 95+%
  • 5 g
  • $ 557.00
  • AK Scientific
  • (2-Methoxy-2-methylpropyl)amine
  • 5g
  • $ 631.00
  • AK Scientific
  • (2-Methoxy-2-methylpropyl)amine
  • 25g
  • $ 2473.00
  • AK Scientific
  • (2-Methoxy-2-methylpropyl)amine
  • 250mg
  • $ 116.00
  • American Custom Chemicals Corporation
  • 2-METHOXY-2-METHYL-1-PROPANAMINE 95.00%
  • 5G
  • $ 2476.74
  • American Custom Chemicals Corporation
  • 2-METHOXY-2-METHYL-1-PROPANAMINE 95.00%
  • 1G
  • $ 1172.71
Total 40 raw suppliers
Chemical Property of 2-Methoxy-2-methylpropan-1-amine
Chemical Property:
  • Vapor Pressure:15.76mmHg at 25°C 
  • Refractive Index:1.417 
  • Boiling Point:119.696°C at 760 mmHg 
  • PKA:8.88±0.10(Predicted) 
  • Flash Point:23.244°C 
  • PSA:35.25000 
  • Density:0.851g/cm3 
  • LogP:1.07040 
  • XLogP3:-0.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:103.099714038
  • Heavy Atom Count:7
  • Complexity:52
Purity/Quality:

97% *data from raw suppliers

2-methoxy-2-methylpropan-1-amine 95+% *data from reagent suppliers

Safty Information:
  • Pictogram(s): Xi 
  • Hazard Codes:Xi 
  • Statements: 43 
  • Safety Statements: 36/37 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(CN)OC
  • Use Description 2-Methoxy-2-methyl-propylamine, also known as tert-butylamine, serves various functions in different fields. In the realm of organic synthesis and chemical manufacturing, it plays a pivotal role as a versatile reagent and building block for the creation of complex organic molecules, contributing to the production of specialty chemicals, pharmaceuticals, and agrochemicals. In the field of analytical chemistry, it can be used as a derivatizing agent for the analysis of various compounds, aiding in the detection and quantification of specific analytes. Additionally, in the production of polymers and plastics, tert-butylamine can serve as a chain transfer agent or catalyst, influencing the molecular weight and properties of the resulting materials. Its applications in organic synthesis, analytical chemistry, and polymer production underscore its significance in driving chemical innovation, supporting precise analysis, and enhancing material properties within these diverse domains.
Technology Process of 2-Methoxy-2-methylpropan-1-amine

There total 11 articles about 2-Methoxy-2-methylpropan-1-amine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With hydrogenchloride; sodium hydroxide; hydrazine; In N-methyl-acetamide; methanol; chloroform; water;
Guidance literature:
With lithium aluminium tetrahydride; In diethyl ether; Inert atmosphere; Reflux;
DOI:10.1002/ejic.201500756
Guidance literature:
With (phthalocyaninato)iron(II); O-pivaloylhydroxylamine trifluoromethanesulfonate salt; at 25 ℃; for 16h; regioselective reaction; Inert atmosphere;
DOI:10.1002/anie.201507630
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