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Bis(2-methoxyethyl)hydroxylamine

HCID 79886
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Basic information

CAS
5815-11-2
Standard SMILES
COCCN(O)CCOC
InChIKey
BJOXIRAGBLTXIZ-UHFFFAOYSA-N
Molecular formula
C6H15NO3
Average molar mass
149.19 g/mol
Monoisotopic mass
149.10519334

Names & identifiers

Preferred name
Bis(2-methoxyethyl)hydroxylamine
IUPAC
N,N-bis(2-methoxyethyl)hydroxylamine
English name
N,N-BIS-(2-METHOXYETHYL)HYDROXYLAMINE
Molecular formula
C6H15NO3
Molecular weight
149.19

Names & synonyms

5815-11-2Ethanamine, N-hydroxy-2-methoxy-N-(2-methoxyethyl)-Bis(2-methoxyethyl)hydroxylamineDTXSID3064013EINECS 227-384-4RefChem:568787DTXCID9042330227-384-4N,N-BIS-(2-METHOXYETHYL)HYDROXYLAMINESCHEMBL4395855BJOXIRAGBLTXIZ-UHFFFAOYSA-NAKOS006285658
Show more names
NS000476291-[hydroxy(2-methoxyethyl)amino]-2-methoxyethaneN-Hydroxy-2-methoxy-N-(2-methoxyethyl)ethan-1-amine

Database identifiers

CAS
5815-11-2
PubChem CID
79886
DTXSID
DTXSID3064013
EC Number
227-384-4
Nikkaji
J43.151F

Properties

Computed structural propertiesFilling in

XLogP
-0.5
Topological polar surface area
41.9 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
4
Rotatable bonds
6
Heavy atoms
10
Formal charge
0
Complexity
62

Physicochemical properties

EPA Substance Registry System
-2 · Ethanamine, N-hydroxy-2-methoxy-N-(2-methoxyethyl)- (5815-11-2)
TSCA
TSCA listed

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

Hazard information

Regulatory InformationChemical: Ethanamine, N-hydroxy-2-methoxy-N-(2-methoxyethyl)-

Safety data

tsca
TSCA listed

Chemistry & industry

Uses & manufacturing

General Manufacturing InformationEthanamine, N-hydroxy-2-methoxy-N-(2-methoxyethyl)-: ACTIVE
Preparation methods · 1 item

PreparationTo a solution of 5.75 gm (0.0825 mole) of hydroxylamine hydrochloride in 25 ml of dimethylsulfoxide (DMSO) and 1.0 ml of water in a 3-necked round bottom flask equipped with a mechanical stirrer, a thermometer, and a condenser is added 22.7 gm (0.27 mole) of sodium bicarbonate. The mixture is stirred and a stream of nitrogen kept throughout the reaction. To this solution is added 33.8 gm (0.182 mole) of 2-methoxyethyl iodide and the stirring continued at 35°C for 20 hr. The temperature is then increased to 50°C, and kept at this temperature for 4 hr. The mixture is made pH 8 by means of 50% sodium hydroxide and extracted several times with 100-ml portions of toluene (original procedure uses benzene), then filtered, and the solids are washed again with toluene. The extracts are dried and concentrated to give 37.0 gm of an oil, which contains (as determined by gas chromatography) 23.0% of bis(3-methoxyethyl)hy-droxylamine (62.7% overall yield) and 9.0% of 2-methoxyethylamine (20.1% yield).

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