N-Methyl-N-(4-hydroxybutyl)nitrosamine

Base Information

Chemical Name:N-Methyl-N-(4-hydroxybutyl)nitrosamine
CAS No.:51938-16-0
Molecular Formula:C₅H₁₂N₂O₂
Molecular Weight:132.162
Hs Code.:
UNII:H3T5WR683M
DSSTox Substance ID:DTXSID20199905
Nikkaji Number:J70.069J
Wikidata:Q83072922
Mol file:51938-16-0.mol

Synonyms:N-Methyl-N-(4-hydroxybutyl)nitrosamine;51938-16-0;CCRIS 1137;1-BUTANOL, 4-(METHYLNITROSAMINO)-;4-(Methylnitrosoamino)-1-butanol;BRN 2238808;N-Nitroso-N-methyl-(4-hydroxybutyl)amine;H3T5WR683M;N-(4-hydroxybutyl)-N-methylnitrous amide;UNII-H3T5WR683M;DTXSID20199905;1-Butanol, 4-(methylnitrosoamino)-;AKOS006278425;LS-46578;METHYL-N-(4-HYDROXYBUTYL)NITROSAMINE, N-

Suppliers and Price of N-Methyl-N-(4-hydroxybutyl)nitrosamine

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

American Custom Chemicals Corporation
N-METHYL-N-(4-HYDROXYBUTYL)NITROSAMINE 95.00%
5MG
$ 503.95

Total 5 raw suppliers

Chemical Property of N-Methyl-N-(4-hydroxybutyl)nitrosamine

Chemical Property:

Vapor Pressure:0.000407mmHg at 25°C
Refractive Index:1.4496 (estimate)
Boiling Point:282°Cat760mmHg
PKA:15.03±0.10(Predicted)
Flash Point:124.3°C
PSA：52.90000
Density:1.08g/cm³
LogP:0.37210
XLogP3:0.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:132.089877630
Heavy Atom Count:9
Complexity:77.4

Purity/Quality:

99% ^*data from raw suppliers

N-METHYL-N-(4-HYDROXYBUTYL)NITROSAMINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(CCCCO)N=O

Technology Process of N-Methyl-N-(4-hydroxybutyl)nitrosamine

There total 1 articles about N-Methyl-N-(4-hydroxybutyl)nitrosamine 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:

: 42042-68-2
4-(N-methylamino)butan-1-ol

: 51938-16-0,74778-52-2,74778-70-4
N-methyl-N-(4-hydroxybutyl)nitrosamine

Guidance literature:: With hydrogenchloride; sodium nitrite;
DOI:10.1248/cpb.26.3891 DOI:10.1016/S0040-4039(00)77919-6

Reference yield:

: 51938-16-0,74778-52-2,74778-70-4
N-methyl-N-(4-hydroxybutyl)nitrosamine

: 61445-55-4
N-nitroso-N-methyl-4-aminobutyric acid

Guidance literature:: With potassium hydroxide; potassium permanganate;
DOI:10.1248/cpb.26.3909

Reference yield:

: 51938-16-0,74778-52-2,74778-70-4
N-methyl-N-(4-hydroxybutyl)nitrosamine

: 70103-63-8
C₁₃H₁₅BrN₂O₄

Guidance literature:: Multi-step reaction with 2 steps

1: aq. KOH, KMnO₄

2: (i) aq. NaOH, (ii) /BRN= 607604/, aq. HCl

With potassium hydroxide; potassium permanganate;
DOI:10.1248/cpb.26.3909