Product Name

  • Name

    1-Heptanol

  • EINECS 203-897-9
  • CAS No. 111-70-6
  • Article Data368
  • CAS DataBase
  • Density 0.822 g/cm3
  • Solubility 2.85 g/L (100 °C) in water
  • Melting Point -36 °C(lit.)
  • Formula C7H16O
  • Boiling Point 176.9 °C at 760 mmHg
  • Molecular Weight 116.203
  • Flash Point 73.9 °C
  • Transport Information
  • Appearance colourless liquid
  • Safety 36-36/37/39-26
  • Risk Codes 20/21/22-36
  • Molecular Structure Molecular Structure of 111-70-6 (1-Heptanol)
  • Hazard Symbols HarmfulXn
  • Synonyms n-Heptyl aloohol;Heptylalcohol (8CI);1-Hydroxyheptane;Enanthic alcohol;Gentanol;NSC 3703;n-Heptan-1-ol;n-Heptanol;n-Heptyl alcohol;
  • PSA 20.23000
  • LogP 1.94910

Synthetic route

heptanal
111-71-7

heptanal

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
With Triethoxysilane; potassium fluoride at 25℃; for 20h;100%
With Triethoxysilane; 1,3-Diphenylpropanone; potassium fluoride at 25℃; for 7h;100%
With 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane In benzene-d6 at 25℃; for 6h; Inert atmosphere; Glovebox; Sealed tube;98%
1-<(tert-butyldimethylsilyl)oxy>heptane
115306-89-3

1-<(tert-butyldimethylsilyl)oxy>heptane

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
With tetrabutyl ammonium fluoride In tetrahydrofuran for 21h; Ambient temperature;100%
With methanol at 20℃; for 2h;100%
sulfonic acid functionalized nanoporous silica In methanol at 35℃; for 1.2h;93%
With water; 2,3-dicyano-5,6-dichloro-p-benzoquinone In ethyl acetate at 20 - 25℃; for 26h;14%
2-(heptyloxy)tetrahydro-2H-pyran
132336-04-0

2-(heptyloxy)tetrahydro-2H-pyran

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
With methanol; Montmorillonite K-10 clay at 20℃; Methanolytic deprotection;97%
With bismuth(lll) trifluoromethanesulfonate In methanol for 0.0833333h; Heating;97%
With Oxone In methanol for 1.25h; Heating;82%
With bismuth(lll) trifluoromethanesulfonate In methanol; N,N-dimethyl-formamide at 110℃; for 24h;67%
3-Butyl-acrolein
2463-63-0

3-Butyl-acrolein

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
With sodium tetrahydroborate; palladium diacetate In methanol at 20℃; for 1h;96%
heptanol trimethylsilyl ether
18132-93-9

heptanol trimethylsilyl ether

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
With Oxone In methanol for 0.15h; Heating;95%
With Nafion-H(R); silica gel In hexane at 20℃; for 0.416667h;95%
With ethylenebis(N-methylimidazolium) chlorochromate In acetonitrile for 1h; Reflux;92%
heptanal
111-71-7

heptanal

C4H10Zn*C2H5Li

C4H10Zn*C2H5Li

A

nonan-3-ol
185019-15-2

nonan-3-ol

B

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
In toluene for 24h; Alkylation; reduction; Title compound not separated from byproducts.;A 95%
B 2%
...Expand
heptanal
111-71-7

heptanal

hexane
110-54-3

hexane

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
With hydrogen In ethanol; benzene95%
2-(heptyloxy)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

2-(heptyloxy)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
With silica gel In methanol at 50℃; for 3h;95%
With methanol; silica gel at 50℃; for 3h;82%
With hydrogenchloride In water
With methanol; silica gel at 50℃; for 1.91667h;88 %Spectr.
2-heptenal

2-heptenal

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
With whole cell cultures of dichomitus albidofuscus at 24℃; for 96h; Darkness; Microbiological reaction;95%
heptyl 4-methylbenzenesulfinate
89149-55-3

heptyl 4-methylbenzenesulfinate

A

1-Bromoheptane
629-04-9

1-Bromoheptane

B

n-heptan1ol
111-70-6

n-heptan1ol

C

1,2-dibromoheptane
42474-21-5

1,2-dibromoheptane

D

toluene-p-sulfonyl bromide
1950-69-2

toluene-p-sulfonyl bromide

Conditions
ConditionsYield
With bromine In chloroform for 2.5h; Ambient temperature;A 89 % Chromat.
B 3 % Chromat.
C 1 % Chromat.
D 94%
...Expand
1-Bromoheptane
629-04-9

1-Bromoheptane

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
With potassium hydroxide; tetrafluoroboric acid; sodium hydrogencarbonate; mercury(II) oxide In tetrahydrofuran 1.) room temp., 3 h;93%
With water; tetra-(n-butyl)ammonium iodide; caesium carbonate In dimethyl sulfoxide at 100℃; for 24h; Schlenk technique;58%
With water; tetra-(n-butyl)ammonium iodide; caesium carbonate; dimethyl sulfoxide at 100℃; for 24h; Schlenk technique; Sealed tube;58%
1-heptyl 4-methylbenzenesulfonate
24767-82-6

1-heptyl 4-methylbenzenesulfonate

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
With cerium(III) chloride; sodium iodide In acetonitrile for 4h; tosylate cleavage; Heating;90%
heptanal
111-71-7

heptanal

ethyl sodium ; compound with diethyl zinc

ethyl sodium ; compound with diethyl zinc

A

nonan-3-ol
185019-15-2

nonan-3-ol

B

tetradecane-7,8-diol
16000-65-0

tetradecane-7,8-diol

C

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
In toluene for 0.166667h; Alkylation; reduction; dimerization; Title compound not separated from byproducts.;A 90%
B 3%
C 2%
...Expand
methoxymethyl heptyl ether
71739-40-7

methoxymethyl heptyl ether

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
phosphotungstic acid In ethanol for 3.5h; Heating;90%
Heptanoic acid chloride
2528-61-2

Heptanoic acid chloride

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
With N-methylpyrrolidine zinc borohydride In tetrahydrofuran at 20℃; for 1.16667h;89%
methyl heptanoate
106-73-0

methyl heptanoate

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
With tert-butyl alcohol In tetrahydrofuran electrolysis (Mg electrodes, LiClO4);88%
With tert-butyl alcohol In tetrahydrofuran Product distribution; Mechanism; electrolysis (Mg electrodes, LiClO4); or Al electrodes;88%
With 5 wt% Re/TiO2; hydrogen In octane at 180℃; under 37503.8 Torr; for 24h; Autoclave; chemoselective reaction;85%
heptanal
111-71-7

heptanal

A

n-heptan1ol
111-70-6

n-heptan1ol

B

oenanthic acid
111-14-8

oenanthic acid

Conditions
ConditionsYield
With (CH3C6H4CH(CH3)2)RuCl((NH2)2C6H4)(1+)*Cl(1-)={(CH3C6H4CH(CH3)2)RuCl((NH2)2C6H4)}Cl; water In 1,4-dioxane at 105℃; for 20h; Schlenk technique; Inert atmosphere;A n/a
B 87%
bei der Einw.von Schweineleber-Brei;
With water; NADPH at 25℃; for 18h; pH=9; aq. buffer; Enzymatic reaction;
n-heptyl formate
112-23-2

n-heptyl formate

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
dodecacarbonyl-triangulo-triruthenium; P(C4H9)3 In pyridine at 180℃; for 10h;86%
ethoxymethyl heptyl ether
1058649-58-3

ethoxymethyl heptyl ether

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
phosphotungstic acid In ethanol for 3.5h; Heating;86%
benzyl hept-1-yl ether
16519-20-3

benzyl hept-1-yl ether

A

n-heptan1ol
111-70-6

n-heptan1ol

B

benzoic acid
65-85-0

benzoic acid

Conditions
ConditionsYield
With bis(acetylacetonate)oxovanadium; methyl 3,5-bis((1H-1,2,4-triazol-1-yl)methyl)benzoate; oxygen; sodium acetate at 120℃; for 48h;A 79%
B 86%
trimethylene oxide
503-30-0

trimethylene oxide

n-butyllithium
109-72-8, 29786-93-4

n-butyllithium

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
With boron trifluoride diethyl etherate In tetrahydrofuran; hexane at -78℃; for 0.166667h;85%
heptanal
111-71-7

heptanal

ethyl potassium ; compound with diethyl zinc

ethyl potassium ; compound with diethyl zinc

A

nonan-3-ol
185019-15-2

nonan-3-ol

B

tetradecane-7,8-diol
16000-65-0

tetradecane-7,8-diol

C

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
In toluene for 0.166667h; Alkylation; reduction; dimerization; Title compound not separated from byproducts.;A 85%
B 9%
C 2%
...Expand
heptyl boronic acid
28741-07-3

heptyl boronic acid

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
With dihydrogen peroxide at 30℃; for 5h; Green chemistry;85%
n-heptanoic anhydride
626-27-7

n-heptanoic anhydride

A

n-heptan1ol
111-70-6

n-heptan1ol

B

oenanthic acid
111-14-8

oenanthic acid

Conditions
ConditionsYield
With methanol; sodium tetrahydroborate In tetrahydrofuran for 1h; Ambient temperature;A 84%
B 78%
With sodium tetrahydroborate; nickel dichloride In diethylene glycol dimethyl ether for 1h; Product distribution; Ambient temperature; other symmetric and mixed anhydrides of carboxylic acids and carboxylic carbonic anhydrides;A 78%
B 80%
N,N-dimethylheptanamide
1115-96-4

N,N-dimethylheptanamide

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
With tert-butyl alcohol In tetrahydrofuran electrolysis (Mg electrodes, LiClO4);82%
(E)-1-ethoxyhept-1-ene
16627-11-5

(E)-1-ethoxyhept-1-ene

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
With chloro-trimethyl-silane; Benzyltriethylammonium borohydride; oxygen In dichloromethane at 0℃; for 6h;80%
oct-1-ene
111-66-0

oct-1-ene

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
With sodium periodate; C18H15ClFN2Ru(1+)*Cl(1-) In water; tert-butyl alcohol at 60℃; for 1h; Catalytic behavior; Schlenk technique; Inert atmosphere;80%
1-Heptene
592-76-7

1-Heptene

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
Stage #1: 1-Heptene With sodium tetrahydroborate; malonic acid In tetrahydrofuran at 60℃; for 5h;
Stage #2: With sodium hydroxide; dihydrogen peroxide In tetrahydrofuran; water at 40 - 50℃; for 2h; Further stages.;		79.5%
Multi-step reaction with 2 steps
2: NaOH; H2O2
View Scheme
butyl magnesium bromide
693-04-9

butyl magnesium bromide

1-chloro-3-hydroxypropane
627-30-5

1-chloro-3-hydroxypropane

n-heptan1ol
111-70-6

n-heptan1ol

Conditions
ConditionsYield
With 1-Phenylprop-1-yne; copper In tetrahydrofuran at 80℃; for 12h;76%
n-heptan1ol
111-70-6

n-heptan1ol

oenanthic acid
111-14-8

oenanthic acid

Conditions
ConditionsYield
With oxygen; potassium carbonate In water at 50℃; for 24h; Green chemistry;100%
With 4-methoxy-TEMPO; sodium hypochlorite; Aliquat 336; potassium bromide In dichloromethane; water at 0℃; for 0.0833333h; pH = 8.6;96%
With dichloro(1,5-cyclooctadiene)ruthenium(II); C30H30N3P2(1+)*Cl(1-); potassium hydroxide In toluene at 120℃; for 24h; Time; Inert atmosphere; Schlenk technique;95%
n-heptan1ol
111-70-6

n-heptan1ol

naphthalen-1-ylsilane
38274-75-8

naphthalen-1-ylsilane

α-Naphthyl-triheptoxy-silan
66774-52-5

α-Naphthyl-triheptoxy-silan

Conditions
ConditionsYield
potassium hydrogencarbonate at 180℃; for 1h;100%
With potassium formate at 180℃;
n-heptan1ol
111-70-6

n-heptan1ol

diphenylsilane
775-12-2

diphenylsilane

Diphenylheptanoxysilan
66774-55-8

Diphenylheptanoxysilan

Conditions
ConditionsYield
potassium thioacyanate at 180℃; for 0.5h;100%
With potassium thioacyanate at 180℃;
n-heptan1ol
111-70-6

n-heptan1ol

diphenylsilane
775-12-2

diphenylsilane

bis-heptyloxy-diphenyl-silane
18784-58-2

bis-heptyloxy-diphenyl-silane

Conditions
ConditionsYield
potassium phthalate at 180℃; for 0.3h;100%
With potassium formate at 180℃;
n-heptan1ol
111-70-6

n-heptan1ol

m-Toluic acid
99-04-7

m-Toluic acid

heptyl 3-methylbenzoate
5462-02-2

heptyl 3-methylbenzoate

Conditions
ConditionsYield
With Candida antarctica lipase B immobilised in a macroporous DVB crosslinked polymer (Novozym 435) In cyclohexane at 80℃; for 24h; Enzymatic reaction;100%
With diphenylphosphinopolystyrene; diethylazodicarboxylate In tetrahydrofuran at 25℃; for 4h;90%
n-heptan1ol
111-70-6

n-heptan1ol

4-nitro-benzoic acid
62-23-7

4-nitro-benzoic acid

heptyl 4-nitrobenzoate
14309-44-5

heptyl 4-nitrobenzoate

Conditions
ConditionsYield
With Candida antarctica lipase B immobilised in a macroporous DVB crosslinked polymer (Novozym 435) In cyclohexane at 80℃; for 24h; Enzymatic reaction;100%
With diphenylphosphinopolystyrene; diethylazodicarboxylate In tetrahydrofuran at 25℃; for 4h;84%
n-heptan1ol
111-70-6

n-heptan1ol

acetic anhydride
108-24-7

acetic anhydride

heptyl acetate
112-06-1

heptyl acetate

Conditions
ConditionsYield
K5 In acetonitrile at 20℃; for 0.416667h;100%
With boron trifluoride diethyl etherate In ethyl acetate for 0.00138889h;100%
With bismuth(lll) trifluoromethanesulfonate In acetonitrile at 20℃; for 0.0833333h;99%
n-heptan1ol
111-70-6

n-heptan1ol

benzoic acid
65-85-0

benzoic acid

1-heptyl benzoate
7155-12-6

1-heptyl benzoate

Conditions
ConditionsYield
With Candida antarctica lipase B immobilised in a macroporous DVB crosslinked polymer (Novozym 435) In cyclohexane at 80℃; for 24h; Solvent; Enzymatic reaction;100%
With 4-nitro-diphenylammonium triflate In toluene at 80℃; for 30h;95%
With zirconocene bis(perfluorooctanesulfonate) trihydrate*(tetrahydrofuran) In neat (no solvent) at 80℃; Sealed tube; Green chemistry; chemoselective reaction;90%
5-methyl-1,10-phenanthroline
3002-78-6

5-methyl-1,10-phenanthroline

n-heptan1ol
111-70-6

n-heptan1ol

3,5-dimethylphenyl iodide
22445-41-6

3,5-dimethylphenyl iodide

1-n-heptyloxy-3,5-dimethyl-benzene

1-n-heptyloxy-3,5-dimethyl-benzene

Conditions
ConditionsYield
With CuI; caesium carbonate In dodecane100%
With CuI; caesium carbonate In dodecane; toluene68%
With CuI; caesium carbonate In dodecane18%
...Expand
n-heptan1ol
111-70-6

n-heptan1ol

p-Toluic acid
99-94-5

p-Toluic acid

1-heptyl 4-methylbenzoate

1-heptyl 4-methylbenzoate

Conditions
ConditionsYield
With Candida antarctica lipase B immobilised in a macroporous DVB crosslinked polymer (Novozym 435) In cyclohexane at 80℃; for 24h; Enzymatic reaction;100%
With 25 wtpercent H3PO4/ZrO2-TiO2 at 130℃; for 1.75h; Neat (no solvent); chemoselective reaction;80%
n-heptan1ol
111-70-6

n-heptan1ol

3-chlorobenzoate
535-80-8

3-chlorobenzoate

n-Heptyl m-chlorobenzoate
80345-34-2

n-Heptyl m-chlorobenzoate

Conditions
ConditionsYield
With Candida antarctica lipase B immobilised in a macroporous DVB crosslinked polymer (Novozym 435) In cyclohexane at 80℃; for 24h; Enzymatic reaction;100%
n-heptan1ol
111-70-6

n-heptan1ol

para-chlorobenzoic acid
74-11-3

para-chlorobenzoic acid

heptyl 4-chlorobenzoate
97222-05-4

heptyl 4-chlorobenzoate

Conditions
ConditionsYield
With Candida antarctica lipase B immobilised in a macroporous DVB crosslinked polymer (Novozym 435) In cyclohexane at 80℃; for 24h; Enzymatic reaction;100%
n-heptan1ol
111-70-6

n-heptan1ol

4-trifluoromethylbenzoic acid
455-24-3

4-trifluoromethylbenzoic acid

heptyl 4-(trifluoromethyl)benzoate
959086-76-1

heptyl 4-(trifluoromethyl)benzoate

Conditions
ConditionsYield
With Candida antarctica lipase B immobilised in a macroporous DVB crosslinked polymer (Novozym 435) In cyclohexane at 80℃; for 24h; Enzymatic reaction;100%
diethylphosphonoacetic acid
3095-95-2

diethylphosphonoacetic acid

n-heptan1ol
111-70-6

n-heptan1ol

heptyl 2-(diethoxyphosphoryl)acetate
147318-09-0

heptyl 2-(diethoxyphosphoryl)acetate

Conditions
ConditionsYield
With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; N-ethyl-N,N-diisopropylamine In ethyl acetate; toluene at 20℃; for 4h; Inert atmosphere;100%
With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; N-ethyl-N,N-diisopropylamine In tetrahydrofuran; ethyl acetate; toluene at 20℃; for 4h; Inert atmosphere;
n-heptan1ol
111-70-6

n-heptan1ol

3,4,6-tri-O-acetyl-2-deoxy-2-fluoro-α-D-mannopyranosyl trichloroacetimidate
154919-05-8

3,4,6-tri-O-acetyl-2-deoxy-2-fluoro-α-D-mannopyranosyl trichloroacetimidate

n-heptyl 3,4,6-tri-O-acetyl-2-fluoro-2-deoxy-α-D-mannopyranoside

n-heptyl 3,4,6-tri-O-acetyl-2-fluoro-2-deoxy-α-D-mannopyranoside

Conditions
ConditionsYield
Stage #1: n-heptan1ol; 3,4,6-tri-O-acetyl-2-deoxy-2-fluoro-α-D-mannopyranosyl trichloroacetimidate In dichloromethane at 20℃; for 0.5h; Molecular sieve; Inert atmosphere;
Stage #2: With trimethylsilyl trifluoromethanesulfonate In dichloromethane at 20℃; for 2h; Molecular sieve; Inert atmosphere;		100%
n-heptan1ol
111-70-6

n-heptan1ol

heptanal
111-71-7

heptanal

Conditions
ConditionsYield
With pyridine chromium peroxide In dichloromethane for 1.25h; Ambient temperature;99%
With polymeric complex of oxodiperoxochromium(VI) compound and pyrazine (Pyz-CrO5)n In dichloromethane for 1.5h; Ambient temperature;99%
With pyridine chromium peroxide In dichloromethane for 1.25h; Product distribution; Ambient temperature; effect of various chromium(VI) based oxidants;99%
n-heptan1ol
111-70-6

n-heptan1ol

methanesulfonyl chloride
124-63-0

methanesulfonyl chloride

heptyl methanesulfonate
16156-51-7

heptyl methanesulfonate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0℃;99%
With triethylamine In dichloromethane at 0 - 20℃;99%
With pyridine at 0℃;
With triethylamine In chloroform at 0 - 5℃; for 0.25h;
n-heptan1ol
111-70-6

n-heptan1ol

acetic acid
64-19-7

acetic acid

heptyl acetate
112-06-1

heptyl acetate

Conditions
ConditionsYield
With bismuth(lll) trifluoromethanesulfonate at 20℃; for 0.5h;99%
With K5 for 0.5h; Heating;98%
With zinc(II) oxide for 3h; Reflux;73%
formic acid
64-18-6

formic acid

n-heptan1ol
111-70-6

n-heptan1ol

n-heptyl formate
112-23-2

n-heptyl formate

Conditions
ConditionsYield
With iodine at 20℃; for 1h; Inert atmosphere;99%
Stage #1: formic acid With silica gel at 20℃; for 0.0166667h;
Stage #2: n-heptan1ol With silica gel at 110℃; for 0.05h;		94%
n-heptan1ol
111-70-6

n-heptan1ol

di(n-butyl)tin oxide
818-08-6

di(n-butyl)tin oxide

1,1,3,3-tetra-n-butyl-1,3-diheptyloxydistannoxane
181116-35-8

1,1,3,3-tetra-n-butyl-1,3-diheptyloxydistannoxane

Conditions
ConditionsYield
at 150℃; for 8h; Inert atmosphere; Industry scale;99%
at 150℃; under 760.051 Torr; for 8.5h; Inert atmosphere; Industry scale;99 %Spectr.
maleic anhydride
108-31-6

maleic anhydride

n-heptan1ol
111-70-6

n-heptan1ol

(3-heptyloxycarbonyl)acrylic acid

(3-heptyloxycarbonyl)acrylic acid

Conditions
ConditionsYield
With triethylamine In dichloromethane at 55℃; under 760.051 Torr; for 1h; Inert atmosphere;99%
n-heptan1ol
111-70-6

n-heptan1ol

N-methylaniline
100-61-8

N-methylaniline

N-heptyl-N-methylaniline
132902-66-0

N-heptyl-N-methylaniline

Conditions
ConditionsYield
With Co2Rh2 nanoparticles immobilized on charcoal at 140℃; for 24h; Schlenk technique; Inert atmosphere; Green chemistry; chemoselective reaction;99%
n-heptan1ol
111-70-6

n-heptan1ol

aniline
62-53-3

aniline

N,N-diheptylaniline

N,N-diheptylaniline

Conditions
ConditionsYield
With Co2Rh2 nanoparticles immobilized on charcoal at 165℃; for 24h; Inert atmosphere; Schlenk technique; Green chemistry; chemoselective reaction;99%
n-heptan1ol
111-70-6

n-heptan1ol

cyclohexanone
108-94-1

cyclohexanone

2,6‐diheptylcyclohexanone
1424337-59-6

2,6‐diheptylcyclohexanone

Conditions
ConditionsYield
With C26H42ClN2Ru(1+)*F6P(1-); potassium hydroxide In toluene at 120℃; for 3h;99%
n-heptan1ol
111-70-6

n-heptan1ol

malonic acid
141-82-2

malonic acid

diheptyl malonate
1117-18-6

diheptyl malonate

Conditions
ConditionsYield
With diphenylammonium trifluoromethanesulfonate In toluene at 80℃; for 6h;98.3%
With sulfuric acid In toluene Fischer-Speier Esterification; Heating;76%
With toluene-4-sulfonic acid In benzene Heating;
n-heptan1ol
111-70-6

n-heptan1ol

heptyl heptanoate
624-09-9

heptyl heptanoate

Conditions
ConditionsYield
With dihydrogen peroxide; bromine In dichloromethane; water at 20℃; for 6h; Solvent;98%
With N-Bromosuccinimide; L-proline In water at 20℃; for 1h;97%
With sodium bromate; sulfuric acid; sodium bromide In water at 20℃; for 24h;97%
n-heptan1ol
111-70-6

n-heptan1ol

citric acid
77-92-9

citric acid

tri(n-heptyl) citrate
95356-26-6

tri(n-heptyl) citrate

Conditions
ConditionsYield
With tetrabutoxytitanium at 170 - 220℃; under 760.051 Torr; for 4.5h; Inert atmosphere; Large scale;98%
With sulfuric acid at 150 - 200℃;
n-heptan1ol
111-70-6

n-heptan1ol

4-Chloro-2-(4-methyl-1-piperazinyl)quinazoline
39213-06-4

4-Chloro-2-(4-methyl-1-piperazinyl)quinazoline

4-Heptyloxy-2-(4-methyl-piperazin-1-yl)-quinazoline
129663-64-5

4-Heptyloxy-2-(4-methyl-piperazin-1-yl)-quinazoline

Conditions
ConditionsYield
With sodium hydride In N,N-dimethyl-formamide98%

1-Heptanol Chemical Properties

IUPAC Name: Heptan-1-ol
Molecular Formula: C7H16O
Molecular Weight: 116.23g/mol
EINECS: 203-897-9
Melting Point: -35 ºC
Freely Rotating Bonds: 6
Polar Surface Area: 9.23 Å2
Index of Refraction: 1.422
Molar Refractivity: 36.01 cm3
Molar Volume: 141.5 cm3
Polarizability: 14.27× 10-24cm3
Surface Tension: 28.5 dyne/cm
Density: 0.82 g/cm3
Flash Point: 73.9 °C
Enthalpy of Vaporization: 48.1 kJ/mol
Boiling Point: 176.9 °C at 760 mmHg
Vapour Pressure: 0.325 mmHg at 25°C 
The Cas Register Number of 1-Heptanol is 111-70-6 .The chemical synonyms of 1-Heptanol (CAS No.111-70-6) are N-Heptanol ; N-Heptyl alcohol ; Alcohol c7 ; 1-Heptanol ; 1-Heptanol alcohol ; Heptyl alcohol ; Heptan-1-ol ; Heptanol .Product categories of 1-Heptanol (CAS No.111-70-6) are 1-Alkanols ; Monofunctional & Alpha,omega-bifunctional Alkanes ; Monofunctional alkanes .The molecular structure of 1-Heptanol (CAS No.111-70-6) is.

1-Heptanol Uses

 1-Heptanol is commonly used in cardiac electrophysiology experiments to block gap junctions and increase axial resistance between myocytes.Because of it has a pleasant smell ,so it is used in cosmetics for its fragrance.

1-Heptanol Toxicity Data With Reference

1.    

ratLD50:500mg/kg

     Archives des Maladies Professionnelles de Medecine du Travail et de SecuriteSociale.Vol. 35, Pg. 501, 1974.
2.    

rabbitLD50:2gm/kg

     Archives des Maladies Professionnelles de Medecine du Travail et de Securite Sociale. Vol. 35, Pg. 501, 1974.
3.    

mouseLD50:1500mg/kg

     Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 31, Pg. 16, 1966.
4.    

mammal (species unspecified)LD50:4350mg/kg

     Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 51(5), Pg. 61, 1986.

1-Heptanol Safety Profile

Hazard Codes: HarmfulXn
Risk Statements: 20/21/22-36 
R20/21/22: Harmful by inhalation, in contact with skin and if swallowed.
R36: Irritating to eyes.
Safety Statements: 36-36/37/39-26
S36: Wear suitable protective clothing.
S36/37/39: Wear suitable protective clothing, gloves and eye/face protection. 
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.  
RIDADR: 2810
WGK Germany: 1
RTECS: MK0350000
HazardClass: 6.1(b)
PackingGroup: III
HS Code: 29051900

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