2-METHOXYETHYLAMINE

2-METHOXYETHYLAMINE Basic information
Product Name:2-METHOXYETHYLAMINE
Synonyms:1-Methoxy-2-aminoethane;RARECHEM AL BW 0200;O-METHYLETHANOLAMINE;2-AMINOETHYL METHYL ETHER;2-METHOXYETHYLAMINE;CAS_109-85-3;2-methoxy-ethanamin;2-Methoxyethanamine
CAS:109-85-3
MF:C3H9NO
MW:75.11
EINECS:203-712-1
Product Categories:Amino Alcohols;Building Blocks;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds
Mol File:109-85-3.mol
2-METHOXYETHYLAMINE Structure
2-METHOXYETHYLAMINE Chemical Properties
Melting point -82 °C
Boiling point 95 °C (lit.)
density 0.864 g/mL at 25 °C (lit.)
refractive index n20/D 1.406(lit.)
Fp 49 °F
storage temp. Store below +30°C.
Water Solubility Completely miscible in water
form clear liquid
pka9.89(at 10℃)
color Colorless to Almost colorless
PH12 (100g/l, H2O, 20℃)
explosive limit3-16.10%(V)
BRN 741854
CAS DataBase Reference109-85-3(CAS DataBase Reference)
EPA Substance Registry SystemEthanamine, 2-methoxy- (109-85-3)
Safety Information
Hazard Codes F,C
Risk Statements 11-34
Safety Statements 16-26-36/37/39-45
RIDADR UN 2733 3/PG 2
WGK Germany 3
RTECS KR8750000
Autoignition Temperature285 °C
TSCA Yes
HazardClass 3
PackingGroup II
HS Code 29221990
ToxicityLD50 orally in Rabbit: 1570 mg/kg
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
2-METHOXYETHYLAMINE Usage And Synthesis
Chemical Propertiesclear colorless liquid
Uses2-Methoxyethylamine is used as a reagent in the preparation of lipid-like materials for delivery of RNAi therapeutics.
General DescriptionKinetics of reaction of 2-methoxyethylamine with guanosine 5′-phospho-2-methylimidazolide (2-MeImpG) was studied.
Purification MethodsAn aqueous 70% solution of the amine is dehydrated by azeotropic distillation with *benzene or methylene chloride and the amine is distilled twice from zinc dust. Store it in a tight container as it absorbs CO2 from the atmosphere. [Beilstein 4 IV 1411.]
4-ETHOXYMETHYLENE-2-PHENYL-2-OXAZOLIN-5-ONE METHYL ISOCYANOACETATE 5-Phenyl-2-(2-propynylamino)-2-oxazolin-4-one 2,2'-Cyclouridine Ethyl N-acetyl-L-tyrosinate hydrate (+)-Bicuculline N-[2-(4-Bromophenoxy)ethyl]pyrrolidine MERSALYL ACID AC-LYS-OME HCL Aspartame Ethyl N-benzoyl-L-tyrosinate Methyl L-tyrosinate N-(4-CHLORO-PHENYL)-OXALAMIC ACID ETHYL ESTER Ethylenebis(oxyethylenenitrilo)tetraacetic acid Ethyl Isocyanatoacetate DIETHYL FORMAMIDOMALONATE Actinomycin D 2-OXO-1-PYRROLIDINEACETIC ACID METHYL ESTER

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