5-CARBOXY-1-PENTANETHIOL

Base Information Edit

Chemical Name:5-CARBOXY-1-PENTANETHIOL
CAS No.:17689-17-7
Molecular Formula:C6H12O2S
Molecular Weight:148.226
Hs Code.:2930909090
Mol file:17689-17-7.mol

Synonyms:5-Carboxy-1-pentanethiol;5-Mercaptopentanecarboxylic acid;6-Mercaptocaproic acid;6-Mercaptohexanoicacid;NSC 310239;e-Mercaptocapronic acid;

Suppliers and Price of 5-CARBOXY-1-PENTANETHIOL

Supply Marketing:Edit

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
6-Mercaptohexanoic acid
50mg
$ 150.00

Sigma-Aldrich
6-Mercaptohexanoic acid 90%
1g
$ 201.00

American Custom Chemicals Corporation
6-MERCAPTOHEXANOIC ACID 95.00%
1G
$ 769.49

Total 13 raw suppliers

Chemical Property of 5-CARBOXY-1-PENTANETHIOL Edit

Chemical Property:

Vapor Pressure:0.00163mmHg at 25°C
Refractive Index:n20/D 1.4846
Boiling Point:273 °C at 760 mmHg
PKA:4.74±0.10(Predicted)
Flash Point:118.9 °C
PSA：76.10000
Density:1.087 g/cm³
LogP:1.56120
Storage Temp.:?20°C

Purity/Quality:

98%,99%, ^*data from raw suppliers

6-Mercaptohexanoic acid ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi
Statements: 36/37/38
Safety Statements: 26

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Uses MHA can be used in the surface modification of InP quantum nanowires for their potential uage in fluorescent chemical sensors that monitor cyanide ions. MHA may also be covalently bonded with liposomes that can form a SAM on the surface of gold for use as an insect odorant receptor in biosensor based applications.

Technology Process of 5-CARBOXY-1-PENTANETHIOL

There total 8 articles about 5-CARBOXY-1-PENTANETHIOL 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: 89.0%

: 4224-70-8
6-bromohexanoic acid

: 17689-17-7
6-mercaptocaproic acid

Guidance literature:: 6-bromohexanoic acid; With thiourea; In methanol; Reflux;

With ammonium hydroxide; In methanol; at 120 ℃; for 2h; Sealed tube;

Reference yield:

: 502-44-3,24980-41-4,80137-66-2
hexahydro-2H-oxepin-2-one

: 17356-08-0
thiourea

: 17689-17-7
6-mercaptocaproic acid

Guidance literature:: hexahydro-2H-oxepin-2-one; thiourea; With hydrogen bromide; In water; at 120 ℃; for 9h; Heating / reflux;

With sodium hydroxide; In water; at 100 ℃; for 3h; Heating / reflux;

With sulfuric acid; In water; at 20 ℃;

Reference yield:

: 6-[(4-methoxy-phenyl)-diphenyl-methylsulfanyl]-hexanoic acid

: 17689-17-7
6-mercaptocaproic acid

Guidance literature:: With N-tris(hydroxymethyl)methyl-2-aminoethanesulfonic acid; trifluoroacetic acid; In dichloromethane; at 20 ℃; for 5h;
DOI:10.1016/S0040-4039(01)01423-X