N-isopropylhydroxylamine

Base Information

Chemical Name:N-isopropylhydroxylamine
CAS No.:5080-22-8
Molecular Formula:C3H9NO
Molecular Weight:75.1106
Hs Code.:2928000090
European Community (EC) Number:225-791-1
UNII:3NT440V34T
DSSTox Substance ID:DTXSID6063694
Nikkaji Number:J203.284H
Wikidata:Q27257766
ChEMBL ID:CHEMBL140282
Mol file:5080-22-8.mol

Synonyms:2-hydroxylaminopropane;2-hydroxylaminopropane sulfate (2:1)

Suppliers and Price of N-isopropylhydroxylamine

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

Matrix Scientific
N-Hydroxypropan-2-amine
10g
$ 2052.00

Matrix Scientific
N-Hydroxypropan-2-amine
5g
$ 1283.00

Matrix Scientific
N-Hydroxypropan-2-amine
1g
$ 443.00

American Custom Chemicals Corporation
N-ISOPROPYLHYDROXYLAMINE 98.00%
2.5KG
$ 6641.80

Total 88 raw suppliers

Chemical Property of N-isopropylhydroxylamine

Chemical Property:

Vapor Pressure:16.5mmHg at 25°C
Melting Point:159-160 °C (dec.)
Boiling Point:104.9 °C at 760 mmHg
PKA:14.14±0.50(Predicted)
Flash Point:44.5 °C
PSA：32.26000
Density:0.886 g/cm³
LogP:0.76450
Water Solubility.:199g/L at 25℃
XLogP3:0.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:75.068413911
Heavy Atom Count:5
Complexity:20.9

Purity/Quality:

99% ^*data from raw suppliers

N-Hydroxypropan-2-amine ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xn
Hazard Codes:Xn
Statements: 21/22
Safety Statements: 24/25

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)NO
Uses N-Isopropylhydroxylamine is used in preparation method of Methylstyrene Butadiene rubber.

Technology Process of N-isopropylhydroxylamine

There total 10 articles about N-isopropylhydroxylamine 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:

Reference yield: 96.0%

: 113768-49-3
2-Isopropyl-3-methyl-5-oxo-2,5-dihydro-isoxazole-4-carboxylic acid ethyl ester

: 5080-22-8
N-isopropylhydroxyamine

Guidance literature:: With hydrogenchloride; acetic acid; In water;
DOI:10.1016/S0040-4039(00)96265-8

Reference yield: 88.0%

: 79-46-9
2-nitropropane

: 75-31-0
isopropylamine

: 5080-22-8
N-isopropylhydroxyamine

Guidance literature:: With hydrogen; In para-xylene; isopropyl alcohol; at 25 ℃; for 4h; under 760.051 Torr;

Reference yield: 85.0%

: 79-46-9
2-nitropropane

: 5080-22-8
N-isopropylhydroxyamine

Guidance literature:: With ammonia borane; gold on titanium oxide; In ethanol; at 20 ℃; for 0.666667h; Inert atmosphere;
DOI:10.1002/adsc.201200983