CAS No.5856-62-2,1-Butanol, 2-amino-,(2S)- Suppliers,MSDS download

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Basic Information

Molecular Structure:
CAS No.:	5856-62-2
Name:	1-Butanol, 2-amino-,(2S)-
Article Data:	37
Cas Database

Formula:	C₄H₁₁NO
Molecular Weight:	89.1374
Synonyms:	(S)-(+)-2-Amino-1-Butanol;D(+)-2-Amino-1-butanol;1-Butanol,2-amino-, (+)- (7CI);1-Butanol, 2-amino-, (S)-;1-Butanol, 2-amino-, (S)-(+)-(8CI);1-Butanol, 2-amino-, d- (4CI);(+)-2-Amino-1-butanol;(+)-2-Aminobutanol;(+)-2-Aminobutyl alcohol;(2S)-2-Aminobutan-1-ol;(S)-2-Amino-1-butanol;(S)-2-Aminobutanol;L-(+)-2-Amino-1-butanol;L-(+)-2-Aminobutanol;L-2-Amino-1-butanol;L-2-Aminobutanol;S-(+)-2-Amino-1-butanol;
EINECS:	227-475-9
Density:	0.927 g/cm³
Melting Point:	-2 °C(lit.)
Boiling Point:	177.2 °C at 760 mmHg
Flash Point:	82.2 °C
Solubility:	1000g/L at 25℃
Appearance:	clear colorless to slightly yellowish viscous
Hazard Symbols:	C
Risk Codes:	34-37-22
Safety:	25 26-36/37/39-45
Transport Information:	UN 2735 8/PG 3
PSA:	46.25000
LogP:	0.41630

Synthetic route

: 1492-24-6
L-2-aminobutyric acid

: 5856-62-2
(S)-2-aminobutan-1-ol

Conditions

Conditions	Yield
With sulfuric acid; hydrogen In water at 90℃; under 3750.38 - 52505.3 Torr; for 8.5h; Reagent/catalyst;	93.7%
With phosphoric acid; hydrogen; pyrographite In water at 65℃; under 18751.9 Torr; for 6.4h; pH=2; Reagent/catalyst; Autoclave;	79.3%
With tetrahydrofuran; lithium aluminium tetrahydride

: 83053-82-1
(1'S)-N-(2'-ethyl-1'-hydroxyethyl)-1H-isoindole-1,3(2H)-dione

: 5856-62-2
(S)-2-aminobutan-1-ol

Conditions

Conditions	Yield
With ethylenediamine In ethanol for 18h; deprotection; Heating;	92%

: 157985-09-6
(-)-(3R,5S)-5-ethyl-3-phenylmorpholin-2-one

: 5856-62-2
(S)-2-aminobutan-1-ol

Conditions

Conditions	Yield
With hydrogen; palladium on activated charcoal In methanol under 112509 Torr; for 72h;	84%
With hydrogen; palladium on activated charcoal In methanol under 114000 Torr; for 72h; Hydrogenolysis; ring cleavage; methanolysis;	84%

: 5077-67-8
1-Hydroxy-2-butanone

: 5856-62-2
(S)-2-aminobutan-1-ol

Conditions

Conditions	Yield
With ammonium hydroxide; formate dehydrogenase; amine dehydrogenase-M0; H3NCH2O2H(1+); nicotinamide adenine dinucleotide In dimethyl sulfoxide at 30℃; for 24h; pH=8.9; Reagent/catalyst; enantioselective reaction;	84%
With (R)-1-phenyl-ethyl-amine; (R)-ω-transaminase from Mycobacterium vanbaalenii; NAD Enzymatic reaction; enantioselective reaction;
With glucose dehydrogenase; ammonium hydroxide; D-glucose; NAD; ammonium chloride; lysozyme; DNase I In water at 40℃; for 24h; pH=9; Catalytic behavior; Kinetics; Temperature; Reagent/catalyst; pH-value; Concentration; Enzymatic reaction; enantioselective reaction;	n/a

: 34114-57-3
N-(1-hydroxybutan-2-yl)-2-phenylacetamide

: 5856-62-2
(S)-2-aminobutan-1-ol

Conditions

Conditions	Yield
With penicillin G acylase; Eupergit C In water at 30℃; for 0.583333h; pH=7.8; Hydrolysis; Enzymatic reaction;	70%

: 909567-51-7
(S)-2-(1,2-dibenzyloxycarbonylhydrazinyl)-1-butanol

: 5856-62-2
(S)-2-aminobutan-1-ol

Conditions

Conditions	Yield
With hydrogen; nickel; acetic acid In methanol under 9000.72 Torr; for 24h;	70%

: 164453-64-9
(3S,6S)-3,6-diethylpiperazine-2,5-dione

: 5856-62-2
(S)-2-aminobutan-1-ol

Conditions

Conditions	Yield
With C24H20ClN2OPRu; potassium tert-butylate; hydrogen In tetrahydrofuran at 110℃; under 2280.15 - 30402 Torr; for 48h; Inert atmosphere; Schlenk technique; Autoclave;	68%

: 26191-63-9
(S)-2-(N-benzylamino)-1-butanol

: 5856-62-2
(S)-2-aminobutan-1-ol

Conditions

Conditions	Yield
With hydrogen; acetic acid; palladium on activated charcoal In methanol for 24h; Ambient temperature;	54%

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

: 5856-62-2
(S)-2-aminobutan-1-ol

Conditions

Conditions	Yield
Stage #1: 2-aminobutanol With O,O'-dibenzoyl-L-tartaric acid In acetone at 25℃; for 6h; Stage #2: With potassium hydroxide In dichloromethane	32%
With L-glutamic acid
With C22H30N6O2(2+)*2Br(1-); copper dichloride In ethanol; water	148 mg
With pyridoxal 5'-phosphate; (R)-1-phenyl-ethyl-amine In aq. phosphate buffer at 30℃; for 6h; pH=7; Enzymatic reaction;	n/a

: 110418-29-6
(S)-(-)-2--1-butanol

: 5856-62-2
(S)-2-aminobutan-1-ol

Conditions

Conditions	Yield
With sodium hydroxide at 80℃; for 2h;

Raw Materials

96-20-8

Downstream Products

150736-72-4

104-13-2

74-55-5

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Specification

The 2-Amino-1-butanol, with the CAS registry number 5856-62-2, is also known as (2S)-2-aminobutan-1-ol. It belongs to the product categories of Pharmaceutical Intermediates; Amino Alcohols (Chiral); Chiral Building Blocks; Synthetic Organic Chemistry; Amino Alcohols; Chiral Building Blocks; Organic Building Blocks. Its EINECS registry number is 227-475-9. This chemical's molecular formula is C₄H₁₁NO and molecular weight is 89.13624. Its IUPAC name is called 2-aminobutan-1-ol. What's more, this chemical is clear colorless to slightly yellowish viscous.

Physical properties of 2-Amino-1-butanol: (1)ACD/LogP: -0.43; (2)ACD/LogD (pH 5.5): -3.52; (3)ACD/LogD (pH 7.4): -2.98; (4)ACD/BCF (pH 5.5): 1; (5)ACD/BCF (pH 7.4): 1; (6)ACD/KOC (pH 5.5): 1; (7)ACD/KOC (pH 7.4): 1; (8)#H bond acceptors: 2; (9)#H bond donors: 3; (10)#Freely Rotating Bonds: 4; (11)Index of Refraction: 1.445; (12)Molar Refractivity: 25.6 cm³; (13)Molar Volume: 96.1 cm³; (14)Surface Tension: 35.3 dyne/cm; (15)Density: 0.927 g/cm³; (16)Flash Point: 82.2 °C; (17)Enthalpy of Vaporization: 48.14 kJ/mol; (18)Boiling Point: 177.2 °C at 760 mmHg; (19)Vapour Pressure: 0.319 mmHg at 25°C.

This product is used in the preparation of emulsifier, surfactant, resin agent, polishing wax, vulcanization accelerator, pharmaceutical raw materials; acid gas absorber. This chemical can be used for the removal of hydrogen sulfide, dihydrogen dioxide. This product is widely used as a derivative of the reagents, reaction promoter.

When you are using this chemical, please be cautious about it as the following:
This chemical may destroy living tissue on contact and may cause burns. In case of contact with eyes, you should rinse immediately with plenty of water and seek medical advice. Whenever you will contact it, please wear suitable protective clothing, gloves and eye/face protection.

You can still convert the following datas into molecular structure:
(1)SMILES: OC[C@@H](N)CC
(2)InChI: InChI=1/C4H11NO/c1-2-4(5)3-6/h4,6H,2-3,5H2,1H3/t4-/m0/s1
(3)InChIKey: JCBPETKZIGVZRE-BYPYZUCNBQ