2-(2-Methoxyethoxy)ethanamine

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2-(2-Methoxyethoxy)ethanamine manufacturers

  • m-PEG2-Amine
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  • 2026-07-15
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  • 2026-07-02
  • CAS:31576-51-9
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2-(2-Methoxyethoxy)ethanamine Basic information
Product Name:2-(2-Methoxyethoxy)ethanamine
Synonyms:2-(2-Methoxyethoxy)ethanamine;MeO-EG(2)-NH2;EthanaMine, 2-(2-Methoxyethoxy)-;Methyl-PEG2-amine;mPEG2-NH2;m-PEG2-amine;Di(ethylene glycol) methyl ether amine;NH2-PEG2-OME
CAS:31576-51-9
MF:C5H13NO2
MW:119.16
EINECS:
Product Categories:MeO-PEG-NH2;peg
Mol File:31576-51-9.mol
2-(2-Methoxyethoxy)ethanamine Structure
2-(2-Methoxyethoxy)ethanamine Chemical Properties
Boiling point 163.7±15.0 °C(Predicted)
density 0.934±0.06 g/cm3(Predicted)
refractive index n/D 1.429
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
pka8.75±0.10(Predicted)
form Solid
color Colourless to Off-White
Stability:Hygroscopic
InChIInChI=1S/C5H13NO2/c1-7-4-5-8-3-2-6/h2-6H2,1H3
InChIKeyQWCGXANSAOXRFE-UHFFFAOYSA-N
SMILESC(N)COCCOC
Safety Information
RIDADR 3265
WGK Germany WGK 3
HazardClass 8
PackingGroup 
HS Code 2922190090
Storage Class6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard ClassificationsAcute Tox. 3 Oral
MSDS Information
2-(2-Methoxyethoxy)ethanamine Usage And Synthesis
Descriptionm-PEG2-amine is a PEG linker containing an amino group. The amino group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The hydrophilic PEG spacer increases solubility in aqueous media.
Uses2-(2-Methoxyethoxy)ethanamine is a reactant in the preparation of cyclopeptoids, a phase-transfer catalyst.
Synthesis
1H-Isoindole-1,3(2H)-dione, 2-[2-(2-methoxyethoxy)ethyl]-

179820-15-6

2-(2-Methoxyethoxy)ethanamine

31576-51-9

2.2.1.3 Synthesis of 2-(2-methoxyethoxy)ethylamine (2d) A mixture of N-[2-(2-methoxyethoxy)ethyl]phthalimide (2c) (27 mmol) and hydrazine monohydrate (43 mmol) in ethanol (30 mL) was refluxed for 3 hours at 100 °C. Upon completion of the reaction, the mixture was cooled to room temperature, filtered, and the filtrate was evaporated. Acetone (50 mL) was added to the residue and the precipitate was filtered. Subsequently, the filtrate was concentrated under reduced pressure to give an orange colored oil 2d in 62% yield. 1H NMR (500 MHz, CDCl3): δ 1.83 (s, 1H), 2.00 (s, 1H), 2.15 (s, 1H), 2.87 (t, J = 5.3 Hz, 1H), 3.35-3.39 (m, 2H), 3.41 (t, J = 6.4 Hz, 1H), 3.50 (t, J = 5.3 Hz, 1H) 3.52-3.55 (m, 2H), 3.60 (dd, J = 5.7, 3.3 Hz, 1H), 3.64 (dd, J = 5.6, 3.8 Hz, 1H), 3.73 (t, J = 6.5 Hz, 1H) ppm; HR ESI-MS (in MeOH): m/z [M + H]+ calcd. 120.0973, found 120.1047. found 120.1047.

IC 50Cleavable Linker; PEGs
References[1] Journal of Organic Chemistry, 2011, vol. 76, # 6, p. 1683 - 1691
[2] Journal of Organic Chemistry, 2010, vol. 75, # 3, p. 598 - 610
[3] Inorganica Chimica Acta, 2016, vol. 452, p. 159 - 169
[4] Patent: WO2009/109035, 2009, A1. Location in patent: Page/Page column 57-58
Tag:2-(2-Methoxyethoxy)ethanamine(31576-51-9) Related Product Information
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