2-Amino-1-butanol supplier | CasNO.5856-62-2

Name
1-Butanol, 2-amino-,(2S)-
EINECS 227-475-9
CAS No. 5856-62-2
Article Data37
CAS DataBase
Density 0.927 g/cm³
Solubility 1000g/L at 25℃
Melting Point -2 °C(lit.)
Formula C₄H₁₁NO
Boiling Point 177.2 °C at 760 mmHg
Molecular Weight 89.1374
Flash Point 82.2 °C
Transport Information UN 2735 8/PG 3
Appearance clear colorless to slightly yellowish viscous
Safety 25 26-36/37/39-45
Risk Codes 34-37-22
Molecular Structure
Hazard Symbols C
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;
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;

: 110418-22-9
(S)-(-)-2-butyl acetate

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

Conditions

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

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

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

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

Conditions

Conditions	Yield
With chiral stationary phase including isopropyl-functionalized CF6 In methanol; acetic acid; triethylamine; acetonitrile at 20℃; Purification / work up;
With glutaraldehyde crosslinked with chitosan In water under 775.743 - 1551.49 Torr; for 10h; Inert atmosphere; Resolution of racemate;

: C4H11NO*C9H11O2PS

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

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

Conditions

Conditions	Yield
With potassium hydroxide Inert atmosphere;

: C4H11NO(1+)*C4H6O6(1-)

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

Conditions

Conditions	Yield
With calcium hydroxide In water pH=10.6;

: C13H19NO2

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

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

C: C13H19NO2

D: C13H19NO2

Conditions

Conditions	Yield
With penicillin G acylase from Bacillus megaterium immobilized on polymethacrylate; purchased from NovoCata (200 U/g); ammonia In water at 40℃; for 32h; pH=7.8; Resolution of racemate; Enzymatic reaction;	A n/a B n/a C n/a D n/a

...Expand

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

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

B: (R)-2-[N-(phenylacetyl)amino]-1-butanol

C: (S)-2-[N-(phenylacetyl)amino]-1-butanol

Conditions

Conditions	Yield
With penicillin G acylase from Bacillus megaterium immobilized on polymethacrylate; purchased from NovoCata (200 U/g); ammonia In water at 40℃; for 6h; pH=7.8; Resolution of racemate; Enzymatic reaction;	A n/a B n/a C n/a

...Expand

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

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

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

C: (R)-2-[N-(phenylacetyl)amino]-1-butanol

D: (S)-2-[N-(phenylacetyl)amino]-1-butanol

Conditions

Conditions	Yield
With penicillin G acylase from Bacillus megaterium immobilized on polymethacrylate; purchased from NovoCata (200 U/g); ammonia In water at 40℃; for 10h; pH=7.8; Resolution of racemate; Enzymatic reaction;	A n/a B n/a C n/a D n/a

...Expand

: C12H16ClNO2

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

B: C12H16ClNO2

Conditions

Conditions	Yield
With penicillin G acylase from Bacillus megaterium immobilized on polymethacrylate; purchased from NovoCata (200 U/g); ammonia In water at 40℃; for 26h; pH=7.8; Resolution of racemate; Enzymatic reaction;	A n/a B n/a

: 106-88-7
ethyloxirane

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

Conditions

Conditions	Yield
With pyridoxal 5'-phosphate; (R)-1-phenyl-ethyl-amine In aq. phosphate buffer; Hexadecane at 30℃; for 5h; pH=7.5; Reagent/catalyst; Green chemistry; Enzymatic reaction;	n/a

: 584-03-2
1,2-dihydroxybutane

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

Conditions

Conditions	Yield
With (R)-1-phenyl-ethyl-amine; (R)-ω-transaminase from Mycobacterium vanbaalenii; 2,3 butanediol dehydrogenase from Bacillus subtilis; polyol dehydrogenase from from Gluconobacter oxydans; NAD at 30℃; pH=7.4; Enzymatic reaction; enantioselective reaction;

: 2491-18-1
(S)-methyl 2-amino-4-(methylthio)butanoate hydrochloride

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

Conditions

Conditions	Yield
With Raney nickel In methanol at 60℃; for 0.2h;

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

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

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

Conditions

Conditions	Yield
With recombinant cyclohexylamine oxidase from Arthrobacter sp. TYUT010-15 In aq. phosphate buffer at 30℃; for 3h; pH=7; Resolution of racemate; Enzymatic reaction;	A n/a B n/a

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

: 24424-99-5
di-tert-butyl dicarbonate

: 150736-72-4
(S)-tert-butyl 1-hydroxybutan-2-ylcarbamate

Conditions

Conditions	Yield
In dichloromethane at 0℃;	100%
With sodium hydroxide In 1,4-dioxane; water at 20℃; for 2h; Inert atmosphere;	100%
With sodium hydroxide In dichloromethane Ambient temperature;	94%

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

: 1352076-45-9
(3S,5R,6R)-3-allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-3-methyltetrahydro-2H-pyran-2-one

: 1388625-18-0
(S)-2-((2R,3R)-2-(3-chlorophenyl)-3-(4-chlorophenyl)-3-hydroxypropyl)-N-((S)-1-hydroxybutan-2-yl)-2-methylpent-4-enamide

Conditions

Conditions	Yield
In toluene at 100℃; for 17h; Inert atmosphere;	99.5%

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

: 1694-92-4
2-Nitrobenzenesulfonyl chloride

: 941584-87-8
(S)-N-(1-hydroxy-butan-2-yl)-2-nitro-benzenesulfonamide

Conditions

Conditions	Yield
Stage #1: (S)-2-aminobutan-1-ol With triethylamine In tetrahydrofuran at 20℃; for 0.166667h; Stage #2: 2-Nitrobenzenesulfonyl chloride In tetrahydrofuran at 20℃; for 0.25h;	99%

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

: 109-90-0
ethyl isocyanate

: 1359050-21-7
(S)-1-ethyl-3-(1-hydroxybutan-2-yl)urea

Conditions

Conditions	Yield
In dichloromethane at 0 - 20℃; for 3h;	99%

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

: 107-06-2
1,2-dichloro-ethane

: 74-55-5
ethambutol

Conditions

Conditions	Yield
In ethanol at 78 - 80℃; for 9.5h; Solvent; Temperature;	98.01%
(heating);

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

: 87-13-8
diethyl 2-ethoxymethylenemalonate

: 1222062-70-5
2-[(1-hydroxymethylpropylamino)methylene]malonic acid diethyl ester

Conditions

Conditions	Yield
In ethanol at 28℃; for 0.5h;	98%

: 1,3,5-tris(4-formylbenzyloxycarbonyl)benzene

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

: 1242079-42-0
1,3,5-tris[4-(S)-(1-hydroxymethylpropylimino)benzyloxycarbonyl]benzene

Conditions

Conditions	Yield
In chloroform at 20℃; for 24h;	98%

: 1,3,5-tris[3,5-bis(4-formylbenzyloxy)benzyloxycarbonyl]benzene

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

: 1,3,5-tris(3,5-bis{4-[1-(S)-hydroxymethylpropylimino]benzyloxy}benzyloxycarbonyl)benzene

Conditions

Conditions	Yield
With sodium sulfate In ethanol for 12h; Reflux;	98%

: (R)-1,1’-spirobiindanyl-7,7’-dicarboxylic acid

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

: (Ra,S,S)-N,N’-bis(1-hydroxybutan-2-yl)-1,1’-spirobiindane-7,7’-dicarboxamide

Conditions

Conditions	Yield
With benzotriazol-1-ol; dicyclohexyl-carbodiimide In tetrahydrofuran at 0 - 20℃; Inert atmosphere; Schlenk technique;	98%

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

: 100-39-0
benzyl bromide

: 249922-60-9
(2S)-N,N-dibenzyl-2-aminobutan-1-ol

Conditions

Conditions	Yield
Stage #1: (S)-2-aminobutan-1-ol With sodium hydroxide; potassium carbonate In methanol for 0.5h; Metallation; Heating; Stage #2: benzyl bromide In methanol for 6h; Alkylation; Heating;	97%
With potassium carbonate In acetonitrile at 20℃; for 24h;	97.3%
With potassium carbonate In acetonitrile at 20℃; for 24h;	97.3%

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

: 58479-61-1
tert-butylchlorodiphenylsilane

: 429669-41-0
(1S)-1-(t-butyldiphenylsilyloxymethyl)propylamine

Conditions

Conditions	Yield
With 1H-imidazole In dichloromethane at 20℃; for 16h;	97%

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

: 24424-99-5
di-tert-butyl dicarbonate

: 79069-13-9
(S)-2-t-butoxycarbonylaminopropan-1-ol

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0 - 20℃; for 6h; Inert atmosphere;	97%

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

: methyl (5-fluoro-2,4-dinitrophenyl)-(S)-prolinate

: methyl (5-(((S)-1-hydroxybutan-2-yl)amino)-2,4-dinitrophenyl)-(S)-prolinate

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 80℃; for 2h; Inert atmosphere;	96.5%

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

: 98-09-9
benzenesulfonyl chloride

: 186246-71-9
(S)-N-benzenesulfonyl-2-amino-1-butanol

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0 - 3℃; for 4h;	96%

: 4282-31-9
Thiophene-2,5-dicarboxylic acid

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

: (-)-2,5-bis[4'-(S)-ethyloxazolin-2'-yl]thiophene

Conditions

Conditions	Yield
In toluene for 24h; Reflux; water segregator;	96%

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

: 105-58-8
Diethyl carbonate

: 13896-06-5
(S)-(-)-4-ethyl-2-oxazolidinone

Conditions

Conditions	Yield
With potassium carbonate at 120℃; for 3h;	96%
With 1,3-dichlorotetrabutyldistannoxane at 80℃; for 1h;	98.5 %Chromat.

: 50-00-0
formaldehyd

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

: 471-25-0
Propiolic acid

: 1,4-bis((S)-4-ethyloxazolidin-3-yl)but-2-yne

Conditions

Conditions	Yield
With copper(l) iodide; copper(ll) bromide In acetonitrile at 60℃; for 0.5h; Microwave irradiation; Sealed tube;	96%

...Expand

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

: 4635-59-0
4-Chlorobutanoyl chloride

: 909566-58-1
1-((S)-1-hydroxybutane-2-yl)pyrrolidin-2-one

Conditions

Conditions	Yield
With potassium hydroxide; sodium sulfate In toluene at 0 - 20℃; for 10h;	95%
With sodium sulfate; potassium hydroxide In toluene at 0℃; for 13h;	80%

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

: 5874-02-2
methyl 2-methylpropanedithioate

: C8H17NOS

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran at 20℃;	95%

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

: 133397-54-3
(R)-2-{[4-(2-methoxyethyl)phenoxy]methyl}oxirane

A: (2S)-2-[[(2R)-2-hydroxy-3-[4-(2-methoxyethyl)phenoxy]propyl]amino]-1-butanol

B: (2S)-2-[[(2S)-2-hydroxy-3-[4-(2-methoxyethyl)phenoxy]propyl]amino]-1-butanol

Conditions

Conditions	Yield
In methanol for 24h;	A 95% B n/a

...Expand

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

: N-(3-fluorobenzyl)-4,6-bis(perfluorophenoxy)-1,3,5-triazin-2-amine

: (S)-2-((4-((3-fluorobenzyl)amino)-6-(perfluorophenoxy)-1,3,5-triazin-2-yl)amino)butan-1-ol

Conditions

Conditions	Yield
Stage #1: N-(3-fluorobenzyl)-4,6-bis(perfluorophenoxy)-1,3,5-triazin-2-amine With N-ethyl-N,N-diisopropylamine In dichloromethane for 0.0833333h; Cooling with ice; Stage #2: (S)-2-aminobutan-1-ol In dichloromethane at 0 - 20℃; for 72.0833h;	95%

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

: 98-59-9
p-toluenesulfonyl chloride

: 79514-33-3
(S) (+)-N-tosyl-2-aminobutanol

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0 - 3℃; for 4h;	94%
With triethylamine In dichloromethane
With triethylamine In dichloromethane at 20℃; for 18h;
Stage #1: (S)-2-aminobutan-1-ol With triethylamine In dichloromethane at 0℃; for 0.0833333h; Stage #2: p-toluenesulfonyl chloride In dichloromethane at 20℃;

: 85-44-9
phthalic anhydride

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

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

Conditions

Conditions	Yield
at 140℃;	93%
at 200℃; for 3h;	92%
at 140℃;
With triethylamine In toluene at 130℃; for 3h; Inert atmosphere; Dean-Stark;

: 67-42-5
ethylene glycol-bis(2-aminoethyl)-N,N,N'N,'-tetraacetic acid

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

: 850410-82-1
(-)-N,N,N',N'-tetrakis{[4-(S)-ethyloxazolin-2-yl]methyl}ethylene glycol bis(2-aminoethyl) ether

Conditions

Conditions	Yield
Stage #1: ethylene glycol-bis(2-aminoethyl)-N,N,N'N,'-tetraacetic acid; (S)-2-aminobutan-1-ol In toluene for 20h; Reflux; Stage #2: at 135℃; for 8h;	93%

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

: 124-38-9
carbon dioxide

: 13896-06-5
(S)-(-)-4-ethyl-2-oxazolidinone

Conditions

Conditions	Yield
With tetrabutylammonium triphenyldifluorosilicate In dimethylsulfoxide-d6 at 150℃; under 760.051 Torr; for 9h; chemoselective reaction;	93%
With caesium carbonate In dimethylsulfoxide-d6 at 25 - 150℃; under 2280.15 Torr; for 24h; Schlenk technique; Autoclave;	51%

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

: 79815-18-2
methyl (3S)-1,2,3,4-tetrahydro-β-carboline-3-carboxylate

: 2'S,3S(-)-1,2,3,4-tetrahydro-β-carboline-3-carboxy-N-(2-butan-1-ol)amide

Conditions

Conditions	Yield
In xylene for 8h; Heating;	92%

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

: 10381-75-6
8-bromotheophylline

: 88080-58-4
(S)-(-)-8-(1-hydroxy-2-butyl)-aminotheophylline

Conditions

Conditions	Yield
In xylene for 20h; Heating;	92%

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

: 81075-61-8
(R)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylic acid methyl ester

: 2'S,3R(+)-1,2,3,4-tetrahydro-β-carboline-3-carboxy-N-(2-butan-1-ol)amide

Conditions

Conditions	Yield
In xylene for 8h; Heating;	91%

2-Amino-1-butanol 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

Product Name

1-Butanol, 2-amino-,(2S)-

Synthetic route

2-Amino-1-butanol Specification

Related Products

Hot Products