4-Phenoxybutan-1-amine

Base Information

Chemical Name:4-Phenoxybutan-1-amine
CAS No.:16728-66-8
Molecular Formula:C10H15 N O
Molecular Weight:165.235
Hs Code.:2922299090
NSC Number:78379
DSSTox Substance ID:DTXSID10276178
Wikidata:Q82006556
Mol file:16728-66-8.mol

Synonyms:4-phenoxybutan-1-amine;16728-66-8;4-phenoxybutylamine;1-Butanamine, 4-phenoxy-;phenoxybutylamine;NSC78379;(4-Phenoxybutyl)amine;4-Phenoxy-1-butanamine;SCHEMBL2528;NCIOpen2_000789;DTXSID10276178;XUOBVRURUPUPHB-UHFFFAOYSA-N;AB7703;MFCD00031400;NSC-78379;AKOS000200977;SB75932;AS-44867;CS-0213123;FT-0694736;EN300-15198

Suppliers and Price of 4-Phenoxybutan-1-amine

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

TRC
4-Phenoxybutan-1-amine
250mg
$ 330.00

Crysdot
4-Phenoxybutan-1-amine 95+%
1g
$ 303.00

Crysdot
4-Phenoxybutan-1-amine 95+%
5g
$ 923.00

American Custom Chemicals Corporation
4-PHENOXYBUTAN-1-AMINE 95.00%
1G
$ 692.46

Alichem
4-Phenoxybutan-1-amine
1g
$ 400.00

AK Scientific
4-Phenoxybutan-1-amine
1g
$ 487.00

Total 6 raw suppliers

Chemical Property of 4-Phenoxybutan-1-amine

Chemical Property:

Vapor Pressure:0.00632mmHg at 25°C
Melting Point:79.5 °C(Solv: ethanol (64-17-5))
Boiling Point:271.8°Cat760mmHg
PKA:10.29±0.10(Predicted)
Flash Point:118.5°C
PSA：35.25000
Density:0.991g/cm³
LogP:2.50460
Storage Temp.:2-8°C
XLogP3:2.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:165.115364102
Heavy Atom Count:12
Complexity:100

Purity/Quality:

99% ^*data from raw suppliers

4-Phenoxybutan-1-amine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)OCCCCN

Technology Process of 4-Phenoxybutan-1-amine

There total 17 articles about 4-Phenoxybutan-1-amine 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: 73.0%

: 124721-39-7
2-(4-phenoxybutyl)-1H-isoindole-1,3(2H)-dione

: 16728-66-8
4-phenoxybutylamine

Guidance literature:: With hydrogenchloride; hydrazine hydrate; In ethanol; for 2h; Reflux;
DOI:10.1002/chem.201704245

Reference yield:

: 64-17-5
ethanol

: 2243-43-8
4-phenoxybutyronitrile

: 6303-58-8
4-phenyloxybutanoic acid

: 16728-66-8
4-phenoxybutylamine

: 4,4'-diphenoxy-dibutyramide

Guidance literature:

Reference yield:

: 5394-18-3
2-(4-bromobutyl)isoindoline-1,3-dione

: 108-95-2,27073-41-2
phenol

: 16728-66-8
4-phenoxybutylamine

Guidance literature:: With sodium hydroxide; potassium carbonate; hydrazine hydrate; In ethanol; water; ethyl acetate; N,N-dimethyl-formamide;