(R)-2-Aminobutan-1-ol

Base Information Edit

Chemical Name:(R)-2-Aminobutan-1-ol
CAS No.:5856-63-3
Molecular Formula:C4H11NO
Molecular Weight:89.1374
Hs Code.:29221990
European Community (EC) Number:227-476-4,687-225-3
UNII:4F725V55LN
DSSTox Substance ID:DTXSID9029275
Nikkaji Number:J9.126J
Wikidata:Q27259516
ChEMBL ID:CHEMBL3184640
Mol file:5856-63-3.mol

Synonyms:5856-63-3;(R)-(-)-2-Amino-1-butanol;(R)-2-Aminobutan-1-ol;(2R)-2-aminobutan-1-ol;(R)-2-Amino-1-butanol;1-Butanol, 2-amino-, (2R)-;2-Amino-1-butanol, (-)-;2-Amino-1-butanol, (R)-;1-Butanol, 2-amino-, (R)-;UNII-4F725V55LN;DTXSID9029275;4F725V55LN;EINECS 227-476-4;L-2-AMINO-1-BUTANOL;[R]-(-)-2-amino-1-butanol;H-Ala-Oet HCl;(-)-2-Aminobutanol;2-Amino-1-butanol #;L-(-)-2-Amino-1-Butanol;(-)-2-amino-1-butanol;R(-)-2-Amino-1-butanol;r-(-)-2-amino-1-butanol;MFCD00064419;2-(R)-aminobutanol;(2R)-2-amino-1-butanol;(R)-2-AMINOBUTANOL;DTXCID409275;(R)-(-)-2amino-1-butanol;(R)-(-)2-amino-1-butanol;CHEMBL3184640;(r)-(-)-2-aminobutan-1-ol;(R)-1-hydroxymethyl-propylamine;(R)-(+)-2-amino-1-butanol;1-Butanol, 2-amino-, (theta)-;Tox21_200478;D-(-)-2-AMINO-1-BUTANOL;AKOS005256337;AM85835;CS-W020734;NCGC00248648-01;NCGC00258032-01;(R)-(-)-2-Amino-1-butanol, 98%;AS-18428;CAS-5856-63-3;A0972;EN300-125884;Q-200022;Q27259516;F1905-7138;Z1203162359

Suppliers and Price of (R)-2-Aminobutan-1-ol

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
(R)-(-)-2-Amino-1-butanol
50mg
$ 50.00

TCI Chemical
(R)-(-)-2-Amino-1-butanol >94.0%(GC)
5mL
$ 44.00

SynQuest Laboratories
(R)-(-)-2-Aminobutan-1-ol
100 g
$ 216.00

SynQuest Laboratories
(R)-(-)-2-Aminobutan-1-ol
5 g
$ 96.00

SynQuest Laboratories
(R)-(-)-2-Aminobutan-1-ol
25 g
$ 128.00

Sigma-Aldrich
(R)-(?)-2-Amino-1-butanol 98%
5g
$ 59.80

Chem-Impex
(R)-(-)-2-Amino-1-butanol,≥98%(Assaybytitration)Hazmat ≥98%(Assaybytitration)
5ML
$ 50.09

Biosynth Carbosynth
(R)-(-)-2-Amino-1-butanol
10 g
$ 120.00

Biosynth Carbosynth
(R)-(-)-2-Amino-1-butanol
5 g
$ 75.00

Biosynth Carbosynth
(R)-(-)-2-Amino-1-butanol
100 g
$ 400.00

Total 124 raw suppliers

Chemical Property of (R)-2-Aminobutan-1-ol Edit

Chemical Property:

Appearance/Colour:clear colorless to light yellow viscous liquid
Melting Point:-2 °C
Refractive Index:n20/D 1.452
Boiling Point:177.2 °C at 760 mmHg
PKA:12.88±0.10(Predicted)
Flash Point:82.2 °C
PSA：46.25000
Density:0.944 g/cm³
LogP:0.41630
Storage Temp.:Store below +30°C.
Sensitive.:Air Sensitive & Hygroscopic
Water Solubility.:Soluble in water
XLogP3:-0.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:89.084063974
Heavy Atom Count:6
Complexity:30.7

Purity/Quality:

99.5%, ^*data from raw suppliers

(R)-(-)-2-Amino-1-butanol ^*data from reagent suppliers

Safty Information:

Pictogram(s): C
Hazard Codes:C
Statements: 34-37-22
Safety Statements: 26-36/37/39-45

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:CCC(CO)N
Isomeric SMILES:CC[C@H](CO)N

Technology Process of (R)-2-Aminobutan-1-ol

There total 16 articles about (R)-2-Aminobutan-1-ol 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: 84.0%

: 5856-63-3
(2R)-2-aminobutan-1-ol

Guidance literature:

Reference yield: 61.0%

: 107-83-5
2-Methylpentane

: 5856-63-3
(2R)-2-aminobutan-1-ol

Guidance literature:

Reference yield: 20.0%

: 96-20-8,13054-87-0
2-aminobutanol

: 5856-63-3
(2R)-2-aminobutan-1-ol

Guidance literature:: 2-aminobutanol; With O,O'-dibenzoyl-L-tartaric acid; In acetone; at 25 ℃; for 6h;

With potassium hydroxide; In dichloromethane;
DOI:10.1055/s-2003-41046