(S)-2-Methylbutylamine

Base Information

Chemical Name:(S)-2-Methylbutylamine
CAS No.:34985-37-0
Molecular Formula:C5H13 N
Molecular Weight:87.1649
Hs Code.:2921199090
European Community (EC) Number:252-307-6
UNII:D8Q8RZF45X
DSSTox Substance ID:DTXSID301311845
Nikkaji Number:J63.092F
Wikidata:Q27276251
Mol file:34985-37-0.mol

Synonyms:(S)-(-)-2-Methylbutylamine;34985-37-0;(S)-2-Methylbutylamine;(2S)-2-methylbutan-1-amine;(S)-2-methylbutan-1-amine;(S)-2-Methylbutylamine, (-)-;UNII-D8Q8RZF45X;D8Q8RZF45X;(s)-1-amino-2-methyl-butane;20626-52-2;EINECS 252-307-6;1-Butanamine, 2-methyl-, (2S)-;2-Methyl-1-butanamine #;S-(-)-2-Methylbutylamine;(S)-(-)-2-Methyl-1-butylamine;(S)-1-Amino-2-methylbutane;2(S)-methylbutylamine;[(2S)-2-methylbutyl]amine;(2S)-2-methyl-1-butylamine;(2S)-2-METHYLBUTYLAMINE;DTXSID301311845;2-METHYLBUTYLAMINE, (S)-;(S)-2-METHYL-1-BUTANAMINE;(S)-2-METHYL-1-BUTYLAMINE;S)-(-)-2-METHYLBUTYLAMINE;MFCD00064430;AKOS006238137;(S)-(-)-2-Methylbutylamine, 95%;AS-60354;1-BUTANAMINE, 2-METHYL-, (S)-;EN300-2977538;A822495;J-019822;Q27276251

Suppliers and Price of (S)-2-Methylbutylamine

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
(S)-(-)-2-Methylbutylamine
50mg
$ 90.00

TRC
(S)-(-)-2-Methylbutylamine
10mg
$ 45.00

Sigma-Aldrich
(S)-(?)-2-Methylbutylamine 95%
1g
$ 156.00

Crysdot
(S)-2-Methylbutan-1-aminehydrochloride 97%
1g
$ 412.00

American Custom Chemicals Corporation
(S)-(-)-2-METHYLBUTYLAMINE 95.00%
5G
$ 912.29

American Custom Chemicals Corporation
(S)-(-)-2-METHYLBUTYLAMINE 95.00%
2.5G
$ 796.77

American Custom Chemicals Corporation
(S)-(-)-2-METHYLBUTYLAMINE 95.00%
1G
$ 619.70

Alfa Aesar
(S)-(-)-2-Methylbutylamine, 98+%
1g
$ 133.00

AK Scientific
(S)-2-Methylbutylamine
250mg
$ 1382.00

Total 18 raw suppliers

Chemical Property of (S)-2-Methylbutylamine

Chemical Property:

Appearance/Colour:CLEAR COLOURLESS TO LIGHT BROWN LIQUID
Vapor Pressure:52.4mmHg at 25°C
Refractive Index:n20/D 1.4126(lit.)
Boiling Point:40-45 °C12 mm Hg(lit.)，92.1 °C at 760 mmHg
PKA:10.75±0.10(Predicted)
Flash Point:38 °F
PSA：26.02000
Density:0.756 g/mL at 20 °C(lit.)
LogP:1.69150
Storage Temp.:Flammables area
Sensitive.:Air Sensitive
Water Solubility.:Fully miscible in water.
XLogP3:1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:87.104799419
Heavy Atom Count:6
Complexity:27.1

Purity/Quality:

97% ^*data from raw suppliers

(S)-(-)-2-Methylbutylamine ^*data from reagent suppliers

Safty Information:

Pictogram(s): FC
Hazard Codes:F,C
Statements: 11-20/21/22-34
Safety Statements: 16-26-36/37/39-45

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:CCC(C)CN
Isomeric SMILES:CC[C@H](C)CN
Uses (S)-(-)-2-Methylbutylamine is used as aintermediate in organic synthesis, as pharmaceutical intermediate.

Technology Process of (S)-2-Methylbutylamine

There total 17 articles about (S)-2-Methylbutylamine 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: 69.0%

: 129539-82-8
(S)-(-)-2-methylbutylamine hydrochloride

: 34985-37-0
(S)-2-methylbutylamine

Guidance literature:: With potassium hydroxide;

Reference yield: 65.0%

: 104835-33-8
(S)-2-(2-methyl-butyl)-isoindole-1,3-dione

: 34985-37-0
(S)-2-methylbutylamine

Guidance literature:: With hydrazine hydrate; In ethanol; for 10h; Heating;
DOI:10.1002/anie.200501332

Reference yield:

: 104835-33-8
(S)-2-(2-methyl-butyl)-isoindole-1,3-dione

: 34985-37-0
(S)-2-methylbutylamine

: 36272-22-7
(R)-(+)-2-methylbutylamine

Guidance literature:: With hydrogenchloride; hydrazine hydrate; Yield given. Multistep reaction. Title compound not separated from byproducts; 1.) methanol, reflux, 2 h, 2.) reflux, 1 h;