1-Pentanethiol

Base Information Edit

Chemical Name:1-Pentanethiol
CAS No.:110-66-7
Molecular Formula:C5H12S
Molecular Weight:104.216
Hs Code.:29309090
European Community (EC) Number:203-789-1
ICSC Number:1521
UN Number:1111
UNII:9A3YK965F3
DSSTox Substance ID:DTXSID9041605
Nikkaji Number:J43.568F
Wikidata:Q3824464
Metabolomics Workbench ID:45541
Mol file:110-66-7.mol

Synonyms:1-Pentanethiol;110-66-7;Pentane-1-thiol;n-Amyl mercaptan;Pentyl mercaptan;AMYL MERCAPTAN;Pentanethiol;Amyl thioalcohol;Pentalarm;Amyl sulfhydrate;Amyl hydrosulfide;Pentylmercaptan;Thioamyl alcohol;n-Pentylmercaptan;1-Mercaptopentane;Mercaptan amylique;n-Pentyl mercaptan;n-Thioamyl alcohol;Amyl mercaptans;1-pentylthiol;1-Pentanthiol;Mercaptan amilique;Caswell No. 642A;Mercaptan amilique [French];Mercaptan amylique [French];HSDB 468;EINECS 203-789-1;EPA Pesticide Chemical Code 100701;BRN 1730979;UNII-9A3YK965F3;9A3YK965F3;1-Pentanethiol, 98%;4-01-00-01653 (Beilstein Handbook Reference);pentanotiol;pentiltiol;pentylthiol;thiopentane;Mercaptopentane;Mercaptopentano;n-pentanethiol;pentilmercaptano;n-pentiltiol;n-Pentylthiol;n-Amylthiol;tioalcohol amilo;1-pentanotiol;1-pentiltiol;Sulfhidrato amilo;1-n-pentanotiol;1-pentane thiol;1-pentane-thiol;pentilmercaptano-n;1-Mercaptopentano;1-n-Pentanethiol;1-pentilmercaptano;1-Pentyl mercaptan;Mercaptano de amilo;hidrosulfuro de amilo;Pentanethiol (6CI);N-mercaptano de amilo;AMM (CHRIS Code);Amyl mercaptan (7CI);PENTANETHIOL, 1-;SCHEMBL37855;UN 1111 (Salt/Mix);AMYL MERCAPTAN [HSDB];CH3(CH2)4SH;1-PENTANETHIOL [FHFI];N-AMYL MERCAPTAN [MI];DTXSID9041605;CHEBI:173322;AMY19243;MFCD00004907;NA1111;UN1111;AKOS015897629;LS-101769;FT-0608200;P0053;EN300-125882;A802231;J-505046;Q3824464

Suppliers and Price of 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
1-Pentanethiol
10mL
$ 60.00

TRC
1-Pentanethiol
5mL
$ 45.00

TCI Chemical
1-Pentanethiol >98.0%(GC)(T)
25mL
$ 53.00

TCI Chemical
1-Pentanethiol >98.0%(GC)(T)
500mL
$ 447.00

Sigma-Aldrich
1-Pentanethiol 98%
1kg
$ 240.00

Sigma-Aldrich
1-Pentanethiol 98%
100 g
$ 217.00

Sigma-Aldrich
1-Pentanethiol 98%
100g-a
$ 210.00

Sigma-Aldrich
1-Pentanethiol 98%
25 g
$ 64.40

Sigma-Aldrich
1-Pentanethiol 98%
25g-a
$ 62.20

Sigma-Aldrich
1-Pentanethiol 98%
sample
$ 40.00

Total 58 raw suppliers

Chemical Property of 1-Pentanethiol Edit

Chemical Property:

Appearance/Colour:clear colorless to light-yellow liquid
Vapor Pressure:27.4 mm Hg ( 37.7 °C)
Melting Point:-76 °C
Refractive Index:n20/D 1.446(lit.)
Boiling Point:126.3 °C at 760 mmHg
PKA:10.51±0.10(Predicted)
Flash Point:18.3 °C
PSA：38.80000
Density:0.832 g/cm³
LogP:2.10640
Storage Temp.:Flammables area
Sensitive.:Air Sensitive
Solubility.:0.16g/l
Water Solubility.:practically insoluble
XLogP3:2.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:104.06597156
Heavy Atom Count:6
Complexity:19.9
Transport DOT Label:Flammable Liquid

Purity/Quality:

99%, ^*data from raw suppliers

1-Pentanethiol ^*data from reagent suppliers

Safty Information:

Pictogram(s): F, Xn
Hazard Codes:F,Xn
Statements: 11-20/22-36/37/38
Safety Statements: 16-23-24/25-37/39-26

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Chemical Classes:Other Classes -> Thiols
Canonical SMILES:CCCCCS
Inhalation Risk:No indication can be given about the rate at which a harmful concentration of this substance in the air is reached on evaporation at 20 °C.
Effects of Short Term Exposure:The substance is irritating to the eyes, skin and respiratory tract.
Uses 1-Pentanethiol is a raw material for organic synthesis. It is mainly used in the organic synthesis of sulfur compounds. 1-Pentanethiol can be used as additives for hair coloring agents.

Technology Process of 1-Pentanethiol

There total 23 articles about 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: 87.0%