2-PENTANOL supplier | CasNO.6032-29-7

Name
2-Pentanol
EINECS 227-907-6
CAS No. 6032-29-7
Article Data296
CAS DataBase
Density 0.809 g/cm³
Solubility 16.6 g/ 100 mL (20 °C ) in water
Melting Point -50 °C
Formula C₅H₁₂O
Boiling Point 118.8 °C at 760 mmHg
Molecular Weight 88.1497
Flash Point 33.9 °C
Transport Information UN 1105 3/PG 3
Appearance clear colourless liquid
Safety 46
Risk Codes 10-20-37-66
Molecular Structure
Hazard Symbols Xn
Synonyms 1-Methyl-1-butanol;1-Methylbutanol;2-Hydroxypentane;2-Pentyl alcohol;DL-2-Pentanol;Methylpropylcarbinol;sec-Amyl alcohol;sec-Pentyl alcohol;
PSA 20.23000
LogP 1.16730

Synthetic route

: 107-87-9
2-Pentanone

: 6032-29-7
(+/-)-2-pentanol

Conditions

Conditions	Yield
With sodium isopropylate; acetonitrile In isopropyl alcohol at 80℃; for 1h; Catalytic behavior;	99%
With formic acid; sodium formate; (η5-C4Ph4COHOC4Ph4-η5)(μ-H)(CO)4Ru2 In water at 100℃; for 3h;	98%
With C40H37ClN2PRuS(1+)*C24H20B(1-); isopropyl alcohol; potassium hydroxide at 82℃; for 2h; Catalytic behavior;	97.7%

: 57984-70-0, 58072-60-9, 90242-65-2, 27301-54-8
Pent-3-yn-2-ol

A: 6032-29-7
(+/-)-2-pentanol

B: 24652-50-4
(Z)-pent-3-en-2-ol

Conditions

Conditions	Yield
With hydrogen; copper-palladium; silica gel In ethanol at 25℃; under 760 Torr; Kinetics;	A n/a B 99%

: 98-01-1
furfural

A: 534-22-5
2-methylfuran

B: 6032-29-7
(+/-)-2-pentanol

C: 71-41-0
pentan-1-ol

D: 107-87-9
2-Pentanone

Conditions

Conditions	Yield
With Cu/SiO2; hydrogen at 220℃; under 760.051 Torr; for 0.5h; Catalytic behavior; Reagent/catalyst; Time; Temperature; Green chemistry;	A 89.5% B n/a C n/a D n/a

...Expand

: 98-01-1
furfural

A: 96-47-9
2-methyltetrahydrofuran

B: 534-22-5
2-methylfuran

C: 6032-29-7
(+/-)-2-pentanol

D: 107-87-9
2-Pentanone

Conditions

Conditions	Yield
With hydrogen; Cu-based catalyst at 212℃; Product distribution; Further Variations:; Temperatures; reaction in vapour phase, fixed bed reactor;	A 3.3% B 88.6% C 4.8% D 2.7%

...Expand

: C26H30O3

: 6032-29-7
(+/-)-2-pentanol

Conditions

Conditions	Yield
With cerium(IV) triflate; water In acetonitrile at 25℃; for 1.25h;	88%

: C13H27BO

: 6032-29-7
(+/-)-2-pentanol

Conditions

Conditions	Yield
With sodium hydroxide In water Inert atmosphere;	87%

: 107-87-9
2-Pentanone

: 68-12-2, 33513-42-7
N,N-dimethyl-formamide

A: 6032-29-7
(+/-)-2-pentanol

B: 57303-85-2
dimethyl-(1-methyl-butyl)-amine

Conditions

Conditions	Yield
With sodium dithionite; sodium hydrogencarbonate In water for 4h; Product distribution; Heating; also also ketones investigated;	A 85% B 13%

...Expand

: 98-00-0
(2-furyl)methyl alcohol

A: 534-22-5
2-methylfuran

B: 6032-29-7
(+/-)-2-pentanol

Conditions

Conditions	Yield
With hydrogen In 1,2-dichloro-ethane at 25℃; under 2250.23 Torr; for 2h; Reagent/catalyst; Time; Sealed tube; Green chemistry;	A 85% B 15%

: C24H26O

: 6032-29-7
(+/-)-2-pentanol

Conditions

Conditions	Yield
With cerium(IV) triflate; water In acetonitrile at 25℃; for 2.83333h;	82%

: 123-54-6
acetylacetone

A: 6032-29-7
(+/-)-2-pentanol

B: 107-87-9
2-Pentanone

C: 1825-14-5, 3950-21-8, 36402-52-5, 42075-32-1, 72345-23-4, 625-69-4
pentane-1,3-diol

Conditions

Conditions	Yield
With samarium diiodide; water In tetrahydrofuran at 20℃; for 0.141667h;	A 78% B 6% C 6%

...Expand

: 625-33-2
3-penten-2-one

A: 6032-29-7
(+/-)-2-pentanol

B: 107-87-9
2-Pentanone

Conditions

Conditions	Yield
With hydrogen; In diethylene glycol dimethyl ether; water at 30℃; under 735.5 Torr; for 5h;	A 7.8% B 77.3%
With nickel kieselguhr at 100℃; under 88260.9 Torr; Hydrogenation;
With nickel kieselguhr at 100 - 160℃; under 88260.9 Torr; Hydrogenation.Hydrieren des Reaktionsprodukts an Kupferchromit; (+-)-pentanol-(2);

: 937-05-3
cis-4-tert-butyl-1-cyclohexanol

: 68-12-2, 33513-42-7
N,N-dimethyl-formamide

A: 6032-29-7
(+/-)-2-pentanol

B: 57303-85-2
dimethyl-(1-methyl-butyl)-amine

Conditions

Conditions	Yield
With sodium dithionite; sodium hydrogencarbonate In water for 4h; Heating;	A 75% B 13%

...Expand

: 98-01-1
furfural

A: 534-22-5
2-methylfuran

B: 6032-29-7
(+/-)-2-pentanol

Conditions

Conditions	Yield
With hydrogen In toluene at 189.84℃; under 15001.5 Torr; for 3h; Catalytic behavior; Kinetics; Temperature; Pressure; Time; Flow reactor;	A 75% B n/a
With hydrogen In toluene at 189.84℃; under 15001.5 Torr; for 3h; Catalytic behavior; Kinetics; Temperature; Pressure; Time; Flow reactor;	A 28% B n/a

: 105-30-6
2-methylpentan-1-ol

A: 6032-29-7
(+/-)-2-pentanol

B: 97-61-0, 22160-39-0
2-Methylpentanoic acid

C: 107-87-9
2-Pentanone

Conditions

Conditions	Yield
With dihydrogen peroxide; methyltrioctylammonium tetrakis(oxodiperoxotungsto)phosphate at 90℃; for 6h;	A n/a B 70% C n/a

...Expand

: 123-15-9
2-methylvaleraldehyde

A: 6032-29-7
(+/-)-2-pentanol

B: 97-61-0, 22160-39-0
2-Methylpentanoic acid

C: 58368-66-4
1-methylbutyl formate

D: 107-87-9
2-Pentanone

Conditions

Conditions	Yield
With dihydrogen peroxide; methyltrioctylammonium tetrakis(oxodiperoxotungsto)phosphate at 90℃; for 0.5h;	A n/a B 70% C 7% D n/a

...Expand

: 98-01-1
furfural

A: 97-99-4
Tetrahydrofurfuryl alcohol

B: 111-29-5
1 ,5-pentanediol

C: 6032-29-7
(+/-)-2-pentanol

D: 71-41-0
pentan-1-ol

Conditions

Conditions	Yield
With hydrogen In isopropyl alcohol at 150℃; under 30003 Torr; for 8h; Temperature; Pressure; Autoclave;	A 68.7% B 24.2% C n/a D n/a

...Expand

: 123-76-2
levulinic acid

A: 96-47-9
2-methyltetrahydrofuran

B: 626-95-9
1,4-Pentanediol

C: 6032-29-7
(+/-)-2-pentanol

D: 108-29-2
5-methyl-dihydro-furan-2-one

Conditions

Conditions	Yield
With hydrogen In water at 150℃; for 4h; Reagent/catalyst; Autoclave;	A 67% B n/a C 9% D 14%

...Expand

: 629-11-8
1,6-hexanediol

: 107-87-9
2-Pentanone

A: 6032-29-7
(+/-)-2-pentanol

B: 7029-23-4
hexadecane-4,13-dione

C: 1047678-69-2
C11H22O2

Conditions

Conditions	Yield
With potassium hydroxide; bis(1,5-cyclooctadiene)diiridium(I) dichloride; 1,7-Octadiene; triphenylphosphine In 1,4-dioxane at 100℃; for 15h; Inert atmosphere;	A 8 %Chromat. B 3 %Chromat. C 66%

...Expand

: 123-76-2
levulinic acid

A: 96-47-9
2-methyltetrahydrofuran

B: 6032-29-7
(+/-)-2-pentanol

C: 71-41-0
pentan-1-ol

Conditions

Conditions	Yield
With hydrogen In water at 150℃; under 37503.8 Torr; for 4h; Autoclave;	A 63% B 18% C 10%

...Expand

: 86692-87-7
hex-5-enyl hydroperoxide

A: 821-41-0
5-Hexen-1-ol

B: 6032-29-7
(+/-)-2-pentanol

C: 764-59-0
hex-5-en-1-al

Conditions

Conditions	Yield
In pentane for 48h; Irradiation;	A 60% B 10% C 30%

...Expand

: 123-76-2
levulinic acid

A: 96-47-9
2-methyltetrahydrofuran

B: 6032-29-7
(+/-)-2-pentanol

Conditions

Conditions	Yield
With hydrogen In water at 150℃; under 37503.8 Torr; for 4h; Autoclave;	A 60% B 18%
Multi-step reaction with 2 steps 1: ruthenium-carbon composite; hydrogen / 1,4-dioxane / 5 h / 30003 Torr / Autoclave 2: ruthenium-carbon composite; hydrogen / isopropyl alcohol / 5 h / 30003 Torr / Autoclave View Scheme
Multi-step reaction with 2 steps 1: hydrogen / water / 100 °C / 30003 Torr / Flow reactor; Green chemistry 2: hydrogen / water / 70 °C / 30003 Torr / Flow reactor; Green chemistry View Scheme

: 123-76-2
levulinic acid

A: 96-47-9
2-methyltetrahydrofuran

B: 626-95-9
1,4-Pentanediol

C: 6032-29-7
(+/-)-2-pentanol

D: 71-41-0
pentan-1-ol

Conditions

Conditions	Yield
With hydrogen In water at 150℃; under 37503.8 Torr; for 4h; Autoclave;	A 60% B 10% C 23% D 6%
With hydrogen In water at 150℃; under 37503.8 Torr; for 4h; Autoclave;	A 25% B 27% C 34% D 7%
With hydrogen In water at 150℃; under 37503.8 Torr; for 4h; Autoclave;

...Expand

: 123-76-2
levulinic acid

A: 6032-29-7
(+/-)-2-pentanol

B: 78-92-2, 15892-23-6
iso-butanol

Conditions

Conditions	Yield
With hydrogen; ruthenium In water at 20℃; under 45004.5 Torr; for 50h;	A 15% B 60%

: 124-38-9
carbon dioxide

: 201230-82-2
carbon monoxide

A: 67-56-1
methanol

B: 71-23-8
propan-1-ol

C: 57-55-6
propylene glycol

D: 626-95-9
1,4-Pentanediol

E: 111-29-5
1 ,5-pentanediol

F: 110-63-4
Butane-1,4-diol

G: 60-29-7
diethyl ether

H: 34557-54-5
methane

I: 64-17-5
ethanol

J: 6032-29-7
(+/-)-2-pentanol

K: 18826-95-4, 107-88-0
1.3-butanediol

L: 5343-92-0
1,2-pentanediol

M: 74-84-0
ethane

N: 74-98-6
propane

O: 115-10-6
Dimethyl ether

P: 540-67-0
ethyl methyl ether

Q: 78-83-1
2-methyl-propan-1-ol

R: 584-02-1
2-pentanol

S: 71-41-0
pentan-1-ol

T: 3174-67-2
1,3-pentanediol

U: 79-20-9
acetic acid methyl ester

V: 67-63-0
isopropyl alcohol

W: 78-92-2, 15892-23-6
iso-butanol

X: 75-65-0
tert-butyl alcohol

Y: 71-36-3
butan-1-ol

Z: 584-03-2
1,2-dihydroxybutane

Conditions

Conditions	Yield
With hydrogen; Cu/Co/Al at 260 - 320℃; under 45004.5 - 75007.5 Torr; Conversion of starting material;	A 57.5% B n/a C n/a D n/a E n/a F n/a G n/a H n/a I 28.5% J n/a K n/a L n/a M n/a N n/a O n/a P n/a Q n/a R n/a S n/a T n/a U n/a V n/a W n/a X n/a Y n/a Z n/a
With hydrogen; Cu/ZnO/Al2O3 at 285 - 300℃; under 45004.5 - 67506.8 Torr; Conversion of starting material;	A 57.5% B n/a C n/a D n/a E n/a F n/a G n/a H n/a I 28.5% J n/a K n/a L n/a M n/a N n/a O n/a P n/a Q n/a R n/a S n/a T n/a U n/a V n/a W n/a X n/a Y n/a Z n/a

...Expand

: 124-38-9
carbon dioxide

: 201230-82-2
carbon monoxide

A: 67-56-1
methanol

B: 71-23-8
propan-1-ol

C: 57-55-6
propylene glycol

D: 626-95-9
1,4-Pentanediol

E: 111-29-5
1 ,5-pentanediol

F: 110-63-4
Butane-1,4-diol

G: 60-29-7
diethyl ether

H: 64-17-5
ethanol

I: 6032-29-7
(+/-)-2-pentanol

J: 18826-95-4, 107-88-0
1.3-butanediol

K: 5343-92-0
1,2-pentanediol

L: 115-10-6
Dimethyl ether

M: 540-67-0
ethyl methyl ether

N: 78-83-1
2-methyl-propan-1-ol

O: 584-02-1
2-pentanol

P: 71-41-0
pentan-1-ol

Q: 3174-67-2
1,3-pentanediol

R: 79-20-9
acetic acid methyl ester

S: 67-63-0
isopropyl alcohol

T: 78-92-2, 15892-23-6
iso-butanol

U: 75-65-0
tert-butyl alcohol

V: 71-36-3
butan-1-ol

W: 584-03-2
1,2-dihydroxybutane

Conditions

Conditions	Yield
With hydrogen; Zn/Cr/K at 350 - 420℃; under 75007.5 - 135014 Torr; Conversion of starting material;	A 57.5% B n/a C n/a D n/a E n/a F n/a G n/a H 28.5% I n/a J n/a K n/a L n/a M n/a N n/a O n/a P n/a Q n/a R n/a S n/a T n/a U n/a V n/a W n/a

...Expand

: 1629-58-9
4-penten-3-one

A: 6032-29-7
(+/-)-2-pentanol

B: 77-84-9
2-ethyl-2-methyl-1,3-propanediol

Conditions

Conditions	Yield
With formaldehyd; hydroquinone In 1,4-dioxane; ethanol	A 57.5% B n/a

: 123-91-1
1,4-dioxane

: 922-63-4
ethylacrolein

A: 6032-29-7
(+/-)-2-pentanol

B: 77-84-9
2-ethyl-2-methyl-1,3-propanediol

Conditions

Conditions	Yield
With formaldehyd; hydroquinone	A 55.9% B n/a

...Expand

: 628-17-1
amyl iodide

A: 646-04-8
(E)-pent-2-ene

B: 6032-29-7
(+/-)-2-pentanol

C: 584-02-1
2-pentanol

D: 71-41-0
pentan-1-ol

E: 109-67-1
1-penten

F: 109-66-0
pentane

Conditions

Conditions	Yield
In acetonitrile for 0.1h; Irradiation;	A 22.18% B 5.91% C 9.26% D 3.15% E 53.6% F 1.41%

...Expand

: 96-47-9
2-methyltetrahydrofuran

A: 6032-29-7
(+/-)-2-pentanol

B: 78-92-2, 15892-23-6
iso-butanol

Conditions

Conditions	Yield
With ruthenium-carbon composite; hydrogen In isopropyl alcohol under 30003 Torr; for 5h; Reagent/catalyst; Autoclave;	A 51.8% B 5.4%

: 123-76-2
levulinic acid

A: 96-47-9
2-methyltetrahydrofuran

B: 6032-29-7
(+/-)-2-pentanol

C: 108-29-2
5-methyl-dihydro-furan-2-one

Conditions

Conditions	Yield
With hydrogen In water; isopropyl alcohol at 150℃; for 4h; Reagent/catalyst; Autoclave;	A 39% B 9% C 51%
With hydrogen In water at 150℃; under 37503.8 Torr; for 4h; Autoclave;	A 28% B 7% C 46%
With hydrogen In water at 150℃; under 37503.8 Torr; for 4h; Autoclave;	A 41% B 8% C 10%

...Expand

: 6032-29-7
(+/-)-2-pentanol

: 109-68-2
2-pentene

Conditions

Conditions	Yield
Deloxan ASP 1/7 acid catalyst In carbon dioxide at 200℃; under 152010 Torr;	100%
With kieselguhr; sulfuric acid at 90 - 110℃;
With sulfuric acid mixtures of cis-and trans-form of pentene-(2);

: 6032-29-7
(+/-)-2-pentanol

: 98-59-9
p-toluenesulfonyl chloride

: 3813-69-2
2-pentyl tosylate

Conditions

Conditions	Yield
With trimethylamine hydrochloride; triethylamine In dichloromethane at 0℃; Inert atmosphere;	100%
With dmap; triethylamine In dichloromethane at 0 - 20℃; for 4h; Inert atmosphere;	92%
With dmap; triethylamine In dichloromethane at 0 - 20℃; for 3h;	92%

: 6032-29-7
(+/-)-2-pentanol

: 107-87-9
2-Pentanone

Conditions

Conditions	Yield
With sodium dichromate; sulfuric acid; silica gel In dichloromethane at 20℃; for 0.5h;	99%
With dihydrogen peroxide In water at 89.84℃; for 5h;	98%
With pyridinium chlorochromate In chloroform at 16℃; for 168h; or 1-methyl imidazolium chlorochromate or imidazolium chlorochromate;	97%

: 536-57-2
p-toluene sulfinic acid

: 6032-29-7
(+/-)-2-pentanol

: sec-pentyl p-toluenesulfinate

Conditions

Conditions	Yield
With dicyclohexyl-carbodiimide at 20℃; for 0.0833333h;	98%
With thionyl chloride; silica gel at 20℃; for 0.666667h;	78%
With silica gel In neat (no solvent) for 0.0166667h; microwave irradiation (900 W);	68%

: 6032-29-7
(+/-)-2-pentanol

: 108-24-7
acetic anhydride

: 626-38-0
2-Pentyl acetate

Conditions

Conditions	Yield
With Methylenediphosphonic acid at 20℃; for 2h; neat (no solvent);	98%
With dmap; triethylamine In dichloromethane at 20℃;	96%
With pyridine at 20℃;	58%
With pyridine at 20℃; for 16h;
With pyridine Inert atmosphere;

: 6032-29-7
(+/-)-2-pentanol

: 611-71-2
(-)-mandelic acid

: 31120-18-0
2-Pentyl Mandelate

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In benzene for 4h; Heating;	97%

: 6032-29-7
(+/-)-2-pentanol

: 100-46-9
benzylamine

: 144782-54-7
N-benzylpentan-2-imine

Conditions

Conditions	Yield
With potassium hydroxide at 30℃; for 6h; Green chemistry;	97%
With air; 3.0 wt % Au-Pd/ZrO2 alloy nanoparticle with Au:Pd molar ratio of 1:1 at 50℃; for 24h; Green chemistry;	66 %Chromat.

: 6032-29-7
(+/-)-2-pentanol

: 89609-13-2
(E)-2,4-Dimethyl-2-pentenoic acid chloride

: 89301-91-7
1-methylbutyl (E)-2,4-dimethyl-2-pentenoate

Conditions

Conditions	Yield
With pyridine In diethyl ether for 2h;	95%

: 6032-29-7
(+/-)-2-pentanol

: 125995-00-8
(S)-(-)-3,3,3-Trifluormilchsaeure

: 245363-05-7
2-pentyl 3,3,3-trifluoro-2-hydroxypropionate

Conditions

Conditions	Yield
In benzene Esterification; Heating;	95%

: 6032-29-7
(+/-)-2-pentanol

: 106-49-0
p-toluidine

: 1020982-57-3
4-methyl-N-(pentan-2-yl)aniline

Conditions

Conditions	Yield
With NiCuFeO(x) In 5,5-dimethyl-1,3-cyclohexadiene for 24h; Inert atmosphere; Sealed tube; Reflux;	95%

: 1003872-51-2
2,6-dichloro-N-cyclohexyl-pyridine-3-carboxamide

: 6032-29-7
(+/-)-2-pentanol

: 6-chloro-N-cyclohexyl-2-(1-methylbutoxy)pyridine-3-carboxamide

Conditions

Conditions	Yield
Stage #1: (+/-)-2-pentanol With sodium hydride In N,N-dimethyl-formamide; mineral oil for 0.75h; Inert atmosphere; Stage #2: 2,6-dichloro-N-cyclohexyl-pyridine-3-carboxamide In N,N-dimethyl-formamide; mineral oil at 0 - 20℃; for 4h; Inert atmosphere;	95%

: 83841-91-2, 55764-37-9
(E)-2-methyl-2-pentenoyl chloride

: 6032-29-7
(+/-)-2-pentanol

: 89301-90-6
1-methylbutyl 2-methylpent-2E-enoate

Conditions

Conditions	Yield
With pyridine In diethyl ether for 2h;	94%

: 541-57-1
4-hydroxy-2(5H)-furanone

: 6032-29-7
(+/-)-2-pentanol

: 133095-79-1
4-(1-Methyl-butoxy)-5H-furan-2-one

Conditions

Conditions	Yield
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran Ambient temperature;	93%

: 6032-29-7
(+/-)-2-pentanol

: 87-69-4
L-Tartaric acid

poly(ethylene glycol) monomethyl ether: poly(ethylene glycol) monomethyl ether

poly(ethylene glycol) monomethyl ether, MW 2000 Da, ester with 1-methylbutyl L-tartrate: poly(ethylene glycol) monomethyl ether, MW 2000 Da, ester with 1-methylbutyl L-tartrate

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In toluene at 115℃; for 45h;	92%

...Expand

: 6032-29-7
(+/-)-2-pentanol

: 5565-32-2
chlorotris(trimethylsilyl)silane

: 2-tris(trimethylsilyl)silyloxypentane

Conditions

Conditions	Yield
With dmap In dichloromethane at 20℃; Inert atmosphere;	92%

: 6032-29-7
(+/-)-2-pentanol

: 14418-84-9
allylsulfonyl chloride

: pent-4-en-2-yl prop-2-ene-1-sulfonate

Conditions

Conditions	Yield
With TEA In dichloromethane at -20 - 20℃; for 4.5h;	92%

: 110-87-2
3,4-dihydro-2H-pyran

: 6032-29-7
(+/-)-2-pentanol

: 2-(2-Pentoxy) tetrahydropyran

Conditions

Conditions	Yield
With 1,5-dichloro-9,10-anthraquinone In dichloromethane for 0.5h; UV-irradiation;	91%
With 1-butyl-3-methylimidazolium hydrogen sulfate for 0.0333333h; microwave irradiation;	90%

: 6032-29-7
(+/-)-2-pentanol

: 123-62-6
propionic acid anhydride

: 54004-43-2
1-methylbutyl propanoate

Conditions

Conditions	Yield
With Cl(1-)C5H14NO(1+)3ZnCl2 In neat (no solvent) at 20℃; for 0.5h; Green chemistry;	91%
With dmap In dichloromethane at 20℃; for 0.166667h;	76%

: 2033-24-1
cycl-isopropylidene malonate

: 6032-29-7
(+/-)-2-pentanol

: 635-93-8
5-chlorosalicyclaldehyde

: pentan-2-yl 6-chloro-2-oxo-2H-chromene-3-carboxylate

Conditions

Conditions	Yield
With iron(III) chloride at 70℃; for 8h;	90%
With iron(III) chloride at 60℃; for 7h; Green chemistry;	87%

...Expand

: 6032-29-7
(+/-)-2-pentanol

: 530114-05-7
2,3,4,6-tetra-O-benzyl-1-O-(N-allylthiocarbamoyl)-β-D-glucopyranose

: 2-pentyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside

Conditions

Conditions	Yield
With bromine; lithium perchlorate; sodium hydrogencarbonate; 4 A molecular sieve In 1,2-dichloro-ethane; N,N-dimethyl-formamide at -25℃; for 0.166667h;	89%

: 2033-24-1
cycl-isopropylidene malonate

: 6032-29-7
(+/-)-2-pentanol

: 1761-61-1
5-bromosalicyclaldehyde

: pentan-2-yl 6-bromo-2-oxo-2H-chromene-3-carboxylate

Conditions

Conditions	Yield
With iron(III) chloride at 70℃; for 8h;	89%

...Expand

: 6032-29-7
(+/-)-2-pentanol

: 75358-95-1
pyridine-2-carboxylic acid naphthalen-1-ylamide

: N-(8-(pentan-2-yloxy)naphthalen-1-yl)picolinamide

Conditions

Conditions	Yield
With cobalt(II) fuoride; caesium carbonate; silver carbonate In 1,2-dichloro-ethane at 110℃; for 24h; regioselective reaction;	89%

: 110-91-8
morpholine

: 6032-29-7
(+/-)-2-pentanol

: 71298-87-8
4-(pentan-2-yl)morpholine

Conditions

Conditions	Yield
With [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; bis[2-(diphenylphosphino)phenyl] ether In 5,5-dimethyl-1,3-cyclohexadiene at 20 - 150℃; for 24.1667h; Inert atmosphere;	88%

: 673-22-3
2-Hydroxy-4-methoxybenzaldehyde

: 2033-24-1
cycl-isopropylidene malonate

: 6032-29-7
(+/-)-2-pentanol

: pentan-2-yl 7-methoxy-2-oxo-2H-chromene-3-carboxylate

Conditions

Conditions	Yield
With iron(III) chloride at 70℃; for 8h;	88%

...Expand

: 1499-29-2
P,P'-methanediyl-bis-phosphonic acid tetrachloride

: 6032-29-7
(+/-)-2-pentanol

: 1498-95-9
tetrakis(1-methylbutyl) methylenebisphosphonate

Conditions

Conditions	Yield
With pyridine In toluene at 20℃; for 3h;	87%

2-PENTANOL Chemical Properties

IUPAC Name: 2-Pentanol
The MF of 2-Pentanol (6032-29-7) is C₅H₁₂O.

The MW of 2-Pentanol (6032-29-7) is 88.15.
Synonyms of 2-Pentanol (6032-29-7): (RS)-2-Pentanol ; 1-Methylbutanol ; 2-Hydroxypentane ; 2-Pentyl alcohol ; Alcoold’amylesecondaire ; Isoamyl alcohol, secondary ; Isoamylalcohol(secondary) ; Isoamylalcohol,secondary
Product Categories: alcohol Flavor
Form: clear colourless liquid
Index of Refraction: 1.405
EINECS: 227-907-6
Density: 0.809 g/ml
Flash Point: 33.9 °C
Boiling Point: 118.8 °C
Melting Point: -50 °C
Storage temp: Flammables area
Water Solubility: 16.6 g/100 mL (20 ºC)
Merck: 14,7119
BRN: 1718819
FEMA: 3316

2-PENTANOL Uses

2-Pentanol (6032-29-7) is used as allowing the use of food with spices, organic synthesis of raw materials and solvents, chromatographic analysis reagent and cotton plastic paint solvent.

2-PENTANOL Toxicity Data With Reference

1.	skn-rbt 500 mg/24H MOD	28ZPAK Sbornik Vysledku Toxixologickeho Vysetreni Latek A Pripravku Marhold, J.V.,Institut Pro Vychovu Vedoucicn Pracovniku Chemickeho Prumyclu Praha,Czechoslovakia.: 1972,36.
2.	eye-rbt 20 mg/24H SEV	28ZPAK Sbornik Vysledku Toxixologickeho Vysetreni Latek A Pripravku Marhold, J.V.,Institut Pro Vychovu Vedoucicn Pracovniku Chemickeho Prumyclu Praha,Czechoslovakia.: 1972,36.
3.	ipr-rat LDLo:2130 mg/kg	JIHTAB Journal of Industrial Hygiene and Toxicology. 27 (1945),1.
4.	orl-rbt LD50:2821 mg/kg	IMSUAI Industrial Medicine and Surgery. 41 (1972),31.

2-PENTANOL Consensus Reports

Reported in EPA TSCA Inventory.

2-PENTANOL Safety Profile

Moderately toxic by ingestion and intraperitoneal routes. A narcotic. A skin and severe eye irritant. Flammable liquid when exposed to heat or flame; can react with oxidizing materials. A severe explosion hazard when exposed to heat or flame. To fight fire, use alcohol foam, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes. See also ALCOHOL, DENATURED; ALCOHOLS, C6-12; ALCOHOLS, C9-11; ALCOHOLS, C12-13, ETHOXYLATED; ALCOHOLS, C12-15, ETHOXYLATED; ALCOHOLS, C12-16, ETHOXYLATED; ALCOHOLS, C14-15, ETHOXYLATED; ALCOHOLS, C16-18, ETHOXYLATED; ALCOHOLS, C8-10, ETHOXYLATED PROPOXYLATED; ALCOHOLS, C12-15, ETHOXYLATED PROPOXYLATED; ALCOHOLS, N.O.S.
Safety information of 2-Pentanol (6032-29-7):
Hazard Codes Xn
Risk Statements
10 Flammable
20 Harmful by inhalation
37 Irritating to the respiratory system
66 Repeated exposure may cause skin dryness or cracking
Safety Statements
46 If swallowed, seek medical advice immediately and show this container or label
RIDADR UN 1105 3/PG 3
WGK Germany 1
RTECS SA4900000
HazardClass 3
PackingGroup III
HS Code 29051500

2-PENTANOL Standards and Recommendations

OSHA PEL: TWA 100 ppm (360 mg/m³); STEL 125 ppm (450 mg/m³)
NIOSH REL: (Isoamyl Alcohol, sec-): TWA 100 ppm; STEL 125 ppm

Product Name

2-Pentanol

Synthetic route

2-PENTANOL Chemical Properties

2-PENTANOL Uses

2-PENTANOL Toxicity Data With Reference

2-PENTANOL Consensus Reports

2-PENTANOL Safety Profile

2-PENTANOL Standards and Recommendations

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