Heptylamine supplier | CasNO.111-68-2

Name
1-Aminoheptane
EINECS 203-895-8
CAS No. 111-68-2
Article Data128
CAS DataBase
Density 0.777
Solubility Soluble in water 6791 mg/L @ 25°C.
Melting Point -23
Formula C7H17 N
Boiling Point 157
Molecular Weight 115.219
Flash Point 44 ºC
Transport Information UN 2734
Appearance CLEAR COLORLESS TO SLIGHTLY YELLOW LIQUID
Safety Poison by intraperitoneal route. A flammable liquid. When heated to decomposition it emits toxic vapors of NO_x.
Risk Codes R10;R34
Molecular Structure
Hazard Symbols
Synonyms Heptylamine(6CI,8CI); 1-Aminoheptane; 1-Heptylamine; NSC 2074; n-Heptylamine
PSA 26.02000
LogP 2.61580

Synthetic route

: 44961-22-0
1-azidoheptane

: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With magnesium In methanol for 0.25h;	98%
With chloro-trimethyl-silane; sodium iodide In acetonitrile for 0.333333h; Ambient temperature;	92%
With samarium diiodide In tetrahydrofuran for 1h; Ambient temperature;	90%

: 111-70-6
n-heptan1ol

: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With aminedehydrogenase; ammonia; ammonium chloride at 30℃; for 48h; pH=8.7; Enzymatic reaction;	91%
Multi-step reaction with 3 steps 1: sulfuric acid; sodium nitrite 2: hydrogen; nickel / 330 - 340 °C 3: nickel; hydrogen / 340 °C View Scheme
Multi-step reaction with 3 steps 1.1: pyridine / dichloromethane / 45 h / 0 - 20 °C / Inert atmosphere 2.1: sodium azide / N,N-dimethyl-formamide / 5 h / 80 °C / Inert atmosphere 3.1: triphenylphosphine / tetrahydrofuran / 22 h / 0 - 20 °C / Inert atmosphere 3.2: 2 h / 20 °C / Inert atmosphere View Scheme
With L-alanin; D-glucose; pyridoxal 5'-phosphate; alanine dehydrogenase from B. subtilis; catalase from M. lysodeikticus; glucose dehydrogenase from DSM; long-chain alcohol oxidase from Aspergillus fumigatus; w-transaminase from Chromobacterium violaceum; NAD; oxygen; ammonium chloride; flavin adenine dinucleotide In aq. phosphate buffer at 20℃; under 1500.15 Torr; for 24h; pH=10; Enzymatic reaction;
With formate dehydrogenase from Candida boidinii; alcohol dehydrogenase from Thermoanaerobacter ethanolicus I86A W110A variant; chimeric amine dehydrogenase generated through domain shuffling of Bb‐PhAmDH variant and L‐AmDH variant, the latter originated from the leucinedehydrogenase from Bacillus stearothermophilus; NADPH oxidase from Bacillus subtilis; nicotinamide adenine dinucleotide phosphate; nicotinamide adenine dinucleotide; catalase In aq. buffer at 30℃; for 12h; pH=8.5; Enzymatic reaction;

: 42955-46-4
heptylurea

: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With sodium hydroxide at 70 - 80℃; for 3h;	90%

: 127611-47-6
(Z)-7-azidohepta-1,3-diene

: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With hydrogen; palladium on activated charcoal In ethanol	90%

: 693-39-0
1-nitroheptane

: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With poly(p-aminostyrene)-palladium(II); hydrogen In N,N-dimethyl-formamide at 70℃; under 760 Torr; for 6h;	89%
With iron; acetic acid

: 127611-45-4
(Z)-7-Azido-hept-3-ene

: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With hydrogen; palladium on activated charcoal In ethanol	87%

: 629-08-3
heptanenitrile

: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With indium(III) chloride; sodium tetrahydroborate In tetrahydrofuran at 25℃; for 4h; Inert atmosphere;	86%
Stage #1: heptanenitrile With borane-2-methyltetrahydrofuran complex In 2-methyltetrahydrofuran at 0℃; for 4h; Heating / reflux; Stage #2: With methanol In 2-methyltetrahydrofuran at 0℃; Product distribution / selectivity;	84.5%
Stage #1: heptanenitrile With borane-THF In tetrahydrofuran at 0℃; for 4h; Heating / reflux; Stage #2: With methanol In tetrahydrofuran at 0℃; Product distribution / selectivity;	80.7%

: 629-04-9
1-Bromoheptane

: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With 5-methyl-1,3,4-thiadiazol-2-amine; triethylamine In ethanol; water at 25℃; for 1h;	85%
With ethanol; ammonia at 100℃;

: 91342-40-4
N-allylheptan-1-amine

: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With tert.-butylhydroperoxide; chromia-pillared montmorillonite catalyst (Cr-PILC) In 2,2,4-trimethylpentane; dichloromethane for 22h; Ambient temperature;	84%

: 629-31-2
1-heptanal oxime

: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With propylamine; lithium; tert-butyl alcohol In ethylenediamine at 20 - 53℃; for 1.75h; Reduction;	55%
With ethanol; platinum under 2206.5 Torr; Hydrogenation;
With ethanol; sodium

: 5730-02-9
N-benzyl-1-heptylamine

A: 111-68-2
1-Heptylamine

B: 143632-83-1
N-heptylbenzamide

Conditions

Conditions	Yield
With tert.-butylhydroperoxide; chromium-pillared montmorillonite In 2,2,4-trimethylpentane; dichloromethane for 26h; Ambient temperature;	A 40% B 48%

: 35601-84-4
methyl N-heptylcarbamate

: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With sodium hydrogen telluride In N,N-dimethyl-formamide at 70 - 75℃; for 5h;	45%
With calcium hydroxide; water

: 629-01-6
n-octanamide

: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With sodium hydroxide; sodium bromite In water at 80℃; for 0.5h;	31%
With 1,4-dioxane; sodium hypochlorite
With potassium hydroxide; bromine
Multi-step reaction with 2 steps 1: methanol; bromine 2: calcium hydroxide; water View Scheme

: 76849-30-4
1-n-heptylthymine

: 109-73-9
N-butylamine

A: 111-68-2
1-Heptylamine

B: 15236-33-6
N-butylthymine

Conditions

Conditions	Yield
With pH 9.5 at 35℃; for 60h; Irradiation;	A 16% B 17 % Turnov.
In water Irradiation;

...Expand

: 111-71-7
heptanal

: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With methanol; ammonia; nickel at 150℃; under 110326 Torr; Hydrogenation;
With ethanol; ammonia; nickel at 90 - 130℃; under 44130.5 Torr; Hydrogenation;
With ethanol; ammonia; hydrogen; nickel
Multi-step reaction with 3 steps 1: KOH 2: 89 percent / KOH / 4 h / 160 °C 3: H2O / 20 °C View Scheme
With imine reductase from Streptomyces ipomoeae; ammonia; NADPH at 30℃; for 0.166667h; Catalytic behavior; Enzymatic reaction;

: 629-06-1
1-Chloroheptane

: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With ammonia; magnesium oxide at 310℃;

: 629-04-9
1-Bromoheptane

A: 2470-68-0
diheptylamine

B: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With methanol; ammonia at 25℃;
With methanol; ammonia

: 629-31-2
1-heptanal oxime

A: 2470-68-0
diheptylamine

B: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With diethyl ether; nickel kieselguhr at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation;
With ethanol; nickel kieselguhr at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation;
With ethanol; nickel at 15 - 18℃; Hydrogenation;
With nickel kieselguhr; methyl cyclohexane at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation;

: 40899-00-1
1-amino-heptan-1-ol

A: 2470-68-0
diheptylamine

B: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With nickel kieselguhr; methyl cyclohexane at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation;
With diethyl ether; nickel kieselguhr at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation;
With ethanol; nickel kieselguhr at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation;
With nickel kieselguhr; 2-Methylcyclohexanone at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation;

: N,N'-diheptylidene-heptane-1,1-diamine

A: 2470-68-0
diheptylamine

B: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With diethyl ether; nickel kieselguhr at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation;
With ethanol; nickel kieselguhr at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation;
With nickel kieselguhr; methyl cyclohexane at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation;

: 6228-45-1
heptanal phenylhydrazone

: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With sodium amalgam; ethanol; acetic acid
With ethanol; aluminium amalgam

: 1798-20-5
N,N'-diheptylurea

: 107-21-1
ethylene glycol

: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
at 175℃; Rate constant;

: 624-09-9
heptyl heptanoate

A: 2470-68-0
diheptylamine

B: 142-82-5
n-heptane

C: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With ammonia; hydrogen; a fused iron catalyst at 280℃; Product distribution; percent of conversion;

...Expand

: 4747-81-3
N-heptylisocyanate

: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With water Yield given;

: complex of α-cyclodextrin with n-heptylamine

A: 111-68-2
1-Heptylamine

B: 10016-20-3
alpha cyclodextrin

Conditions

Conditions	Yield
With phosphate buffer In water-d2 at 25℃; Equilibrium constant; Thermodynamic data; standard molar enthalpy ΔrH0, standard molar Gibbs energy ΔrG0, standard molar entropy ΔrS0;
In alkaline aq. solution at 25℃; pH=11.60; Equilibrium constant; dissociation;

: 38427-89-3
(N-tert-Butyloxycarbonyl)heptylamine

: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
With trifluoroacetic acid Deacylation;

: 123-91-1
1,4-dioxane

: 628-62-6
heptanamide

copper-chromium-oxide: copper-chromium-oxide

A: 2470-68-0
diheptylamine

B: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
at 175 - 250℃; under 73550.8 - 220652 Torr; Hydrogenation;

...Expand

: 71-41-0
pentan-1-ol

: 628-62-6
heptanamide

sodium: sodium

A: 111-70-6
n-heptan1ol

B: 111-68-2
1-Heptylamine

...Expand

: 110-86-1
pyridine

: 592-76-7
1-Heptene

ammonium thiosulfate: ammonium thiosulfate

: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
at 155℃;

...Expand

: 592-76-7
1-Heptene

aqueous ammonium polysulfide: aqueous ammonium polysulfide

: 111-68-2
1-Heptylamine

Conditions

Conditions	Yield
at 155℃;

: 111-68-2
1-Heptylamine

: 79-50-5
pantolactone

: 43180-77-4
N-heptyl-2,4-dihydroxy-3,3-dimethylbutyramide

Conditions

Conditions	Yield
In methanol at 20℃; for 20h;	100%
at 100 - 110℃;
at 100 - 110℃;

: 506-68-3
bromocyane

: 111-68-2
1-Heptylamine

: 87888-05-9
heptyl cyanamide

Conditions

Conditions	Yield
	100%
With diethyl ether

: 111-68-2
1-Heptylamine

: 598-21-0
2-Bromoacetyl bromide

: 5463-16-1
2-bromo-N-heptylacetamide

Conditions

Conditions	Yield
With potassium carbonate In dichloromethane; water at 0 - 20℃; for 6.5h;	100%
In tetrahydrofuran; water	99%
In tetrahydrofuran; water	99%
In tetrahydrofuran; water	99%
With 1,2-dichloro-ethane at -10℃;

: 111-68-2
1-Heptylamine

: 98-59-9
p-toluenesulfonyl chloride

: 124920-13-4
N-heptyl-4-methylbenzenesulfonamide

Conditions

Conditions	Yield
With dmap; triethylamine In dichloromethane at 0 - 20℃; for 12h;	100%
With ethanol
With triethylamine In dichloromethane at 0 - 20℃;
With triethylamine In dichloromethane at 0 - 25℃;

: 111-68-2
1-Heptylamine

: 96224-27-0
4-neopentylbenzoyl chloride

: 96224-28-1
4-(2,2-Dimethyl-propyl)-N-heptyl-benzamide

Conditions

Conditions	Yield
With triethylamine Ambient temperature;	100%

: 111-68-2
1-Heptylamine

: 124-63-0
methanesulfonyl chloride

: 103085-20-7
N-methylsulfonylheptylamine

Conditions

Conditions	Yield
With dmap; triethylamine In dichloromethane at 0 - 20℃; for 12h;	100%
With triethylamine In diethyl ether for 0.5h; Heating;	83%
In tetrahydrofuran

: 111-68-2
1-Heptylamine

: 110-13-4
2,5-hexanedione

: N-heptyl-2,5-dimethylpyrrole

Conditions

Conditions	Yield
at 150℃; Paal-Knorr Pyrrole Synthesis;	100%
With Fe(3+)-montmorillonite K10 In dichloromethane at 20℃; for 2h; Paal-Knorr condensation;	93%
With [BMIm]I at 25℃; for 0.5h; Paal-Knorr condensation;	95 % Chromat.
With aminosulfonic acid at 18℃; for 0.5h;	98 % Chromat.

: 35265-83-9
2,4-dichloro-7-methylthieno[3,2-d]pyrimidine

: 111-68-2
1-Heptylamine

: 221043-53-4
2-chloro-4-heptylamino-7-methylthieno[3,2-d]pyrimidine

Conditions

Conditions	Yield
In (2S)-N-methyl-1-phenylpropan-2-amine hydrate; N,N-dimethyl-formamide	100%
In water; N,N-dimethyl-formamide at 0 - 20℃; for 2h;	100%

: 111-68-2
1-Heptylamine

: 306935-82-0
1-chloro-4-isothiocyanato-2,5-dimethoxybenzene

: 1159073-79-6
1-(4-chloro-2,5-dimethoxyphenyl)-3-heptylthiourea

Conditions

Conditions	Yield
In chloroform at 20℃;	100%

: 111-68-2
1-Heptylamine

: 124-38-9
carbon dioxide

: 59734-16-6
N-n-heptylformamide

Conditions

Conditions	Yield
With C21H24N2; phenylsilane In tetrahydrofuran at 20℃; under 750.075 - 2250.23 Torr; for 22h; Reagent/catalyst; Solvent; Temperature; Time; Concentration; Inert atmosphere; Glovebox;	100%
With C21H39Cl2CoNP2; potassium tert-butylate; hydrogen; sodium triethylborohydride In toluene at 150℃; under 22502.3 Torr; for 36h; Autoclave;	99%
With C12H14N4Ir(1+)C8H12I(1-)C3H7NO; hydrogen In methanol at 100℃; under 45004.5 Torr; for 20h; Autoclave;	97%

: 111-68-2
1-Heptylamine

: 5880-06-8
(7-(carboxymethyl)-1,3,6,8-tetraoxo-3,6,7,8-tetrahydro-1H-benzo[lmn][3,8]phenanthrolin-2-yl)-acetic acid

: C18H10N2O8*2C7H17N

Conditions

Conditions	Yield
In methanol at 20℃;	100%

: 111-68-2
1-Heptylamine

: 79-04-9
chloroacetyl chloride

: 2-chloro-N-heptylacetamide

Conditions

Conditions	Yield
With potassium carbonate In dichloromethane at 20℃; for 2.16667h; Inert atmosphere; Reflux;	100%
With potassium carbonate In acetone Reflux;	89%

: 111-68-2
1-Heptylamine

: 79-08-3
bromoacetic acid

: C54H104N6O7

Conditions

Conditions	Yield
Stage #1: bromoacetic acid With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 1h; Stage #2: 1-Heptylamine In N,N-dimethyl-formamide at 20℃; for 0.666667h; Stage #3: bromoacetic acid Further stages;	100%

: 111-68-2
1-Heptylamine

: 100-52-7
benzaldehyde

: 58979-19-4
N-(phenylmethylene)-1-heptanamine

Conditions

Conditions	Yield
In methanol for 3h; Ambient temperature;	99.8%
With Montmorillonite K10 clay Condensation; microwave irradiation;
With magnesium sulfate In dichloromethane at 20℃;
With alizarin red S-sensitized TiO2 In acetonitrile for 0.5h;

: 111-68-2
1-Heptylamine

: 201230-82-2
carbon monoxide

: 1798-20-5
N,N'-diheptylurea

Conditions

Conditions	Yield
With palladium; oxygen; potassium iodide In 1,4-dioxane at 130℃; under 30003 Torr; for 24h; Autoclave; Green chemistry;	99%
Stage #1: 1-Heptylamine; carbon monoxide With sulfur at 80℃; under 760.051 Torr; for 4h; Stage #2: With oxygen at 20℃; under 760.051 Torr; for 1h; Further stages.;	81%
With iron(III) oxide; selenium; 3-trifluoromethylnitrobenzene In tetrahydrofuran at 64℃; under 760 Torr; for 2h;	69%
With oxygen; potassium iodide In neat (no solvent) at 122℃; for 6h; Green chemistry;	58%

: 498-62-4
3-thiophene carboxaldehyde

: 111-68-2
1-Heptylamine

: N-(3-thienylmethylene)-n-heptylamine

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In toluene for 3h; Heating;	99%

: 111-68-2
1-Heptylamine

: 629-08-3
heptanenitrile

Conditions

Conditions	Yield
With C22H22Cl2FeN2O8(2-)*2C16H36N(1+); oxygen In neat (no solvent) at 100℃; under 760.051 Torr; for 0.5h; Green chemistry;	99%
With tetrabutylammomium bromide; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione In acetonitrile at 20℃; for 0.0833333h; Inert atmosphere; Molecular sieve;	89%
With dichloro(1,5-cyclooctadiene)ruthenium(II); hexamethylenetetramine In toluene for 24h; Schlenk technique; Inert atmosphere; Reflux;	80%
With dichloro(benzene)ruthenium(II) dimer; hexamethylenetetramine In toluene for 24h; Schlenk technique; Inert atmosphere; Reflux; Green chemistry;	72%
With rhodium(III) chloride hydrate; C13H19N4(1+)*Br(1-) In toluene at 110℃; for 24h; Schlenk technique; Inert atmosphere;	72%

: 111-68-2
1-Heptylamine

: 90-02-8
salicylaldehyde

: 2-[(E)-(heptylimino)methyl]phenol

Conditions

Conditions	Yield
With magnesium sulfate In dichloromethane at 20℃;	99%

: 111-68-2
1-Heptylamine

: 1422642-91-8
1-(3-chloroquinoxalin-2-yl)-3-phenylprop-2-yn-1-one

: 1422642-95-2
1-heptyl-2-phenylpyrido[2,3-b]quinoxalin-4(1H)-one

Conditions

Conditions	Yield
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In N,N-dimethyl-formamide at 160℃; for 16h; Inert atmosphere;	99%

: 111-68-2
1-Heptylamine

: 111-27-3
hexan-1-ol

: 93717-22-7
N-heptylhexanamide

Conditions

Conditions	Yield
With C24H21ClN2OPRu; potassium tert-butylate In toluene for 24h; Reflux; Inert atmosphere;	99%
With potassium tert-butylate; [Ru(PtBuNNHBn)H(CO)Cl] In diethyl ether at 50℃; under 760.051 Torr; for 22h; Reagent/catalyst; Inert atmosphere;	85%

: 108-05-4
vinyl acetate

: 111-68-2
1-Heptylamine

: 14202-55-2
N-heptylacetamide

Conditions

Conditions	Yield
With immobilization of Candida cylindracea lipase In hexane at 55℃; for 14h;	99%

: 111-68-2
1-Heptylamine

: 73033-58-6
5-chloro-2-nitrobenzyl alcohol

: C14H19ClN2O

Conditions

Conditions	Yield
In water; butan-1-ol at 20℃; for 3h; UV-irradiation;	99%

: 64-18-6
formic acid

: 111-68-2
1-Heptylamine

: 59734-16-6
N-n-heptylformamide

Conditions

Conditions	Yield
With 4-methyl-morpholine; dmap; 2-chloro-4,6-dimethoxy-1 ,3,5-triazine In dichloromethane for 8h; Heating;	98%

: 111-68-2
1-Heptylamine

: 2470-68-0
diheptylamine

Conditions

Conditions	Yield
With Co2Rh2/C In toluene at 180℃; under 760.051 Torr; for 18h; Autoclave; Inert atmosphere;	98%
With hydrogen; nickel at 200℃; under 73550.8 Torr;
Multi-step reaction with 2 steps 1: 85 percent / triethylamine / tetrahydrofuran / 0.25 h / 2.5 - 20 °C 2: 84 percent / lithium aluminum hydride / diethyl ether / Heating View Scheme
Multi-step reaction with 2 steps 1: 97 percent / DMAP; Et3N / CH2Cl2 / 24 h / 20 °C 2: 99 percent / LiAlH4 / tetrahydrofuran / 24 h / Heating View Scheme

: 111-68-2
1-Heptylamine

: 75-36-5
acetyl chloride

: 14202-55-2
N-heptylacetamide

Conditions

Conditions	Yield
With pyridine In dichloromethane at 0 - 20℃;	98%
With pyridine In dichloromethane at 0 - 20℃; for 1.03333h;	98%
With pyridine In benzene

: 111-68-2
1-Heptylamine

: 30818-49-6
benzene-1,2-bis(sulphenyl chloride)

: 1025977-43-8
N-heptyl-1,3,2-benzodithiazole

Conditions

Conditions	Yield
With triethylamine In diethyl ether 1.) -20 deg C, 1 h, 2.) RT, 16 h;	98%

: 670-28-0
3-Acetyl-4-methoxy-6-methyl-2-pyranone

: 111-68-2
1-Heptylamine

: 3-Acetyl-4-(1-heptylamino)-6-methylpyran-2-one

Conditions

Conditions	Yield
In benzene for 24h; Substitution;	98%

: 111-68-2
1-Heptylamine

: 1521-38-6
2,3-dimethoxybenzoic acid

: (i)-N-Heptyl-2,3-dimethoxybenzamide

Conditions

Conditions	Yield
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃;	98%

: 111-68-2
1-Heptylamine

A: 22791-80-6
4,4-dimethyl-tetrahydro-pyran-2-one

B: 139773-01-6
N-heptyl-3,3-dimethyl-5-hydroxypentanamide

Conditions

Conditions	Yield
In toluene	A 98% B n/a

Heptylamine Chemical Properties

IUPAC Name: Heptan-1-amine
The MF of Heptylamine (CAS NO.111-68-2) is C₇H₁₇N.

The MW of Heptylamine (CAS NO.111-68-2) is 115.22.
Synonyms of Heptylamine (CAS NO.111-68-2): N-Heptylamine ; Heptan-1-amine ; 1,4-Dicyanobutane ; 1-Heptylamine ; Heptylamine
Product Categories: Alkylamines;Monofunctional & alpha,omega-Bifunctional Alkanes
Apperance: clear colorless to slightly yellow liquid
Index of Refraction: 1.427
EINECS: 203-895-8
Density: 0.779 g/ml
Flash Point: 35 °C
Boiling Point: 156.4 °C
Melting Point: -23 °C
Storage temp: Flammables area
Sensitive: Air Sensitive
BRN: 1731688

Heptylamine Uses

Heptylamine (CAS NO.111-68-2) is used as a solvent,also used in organic synthesis .

Heptylamine Production

Heptanal oxime (see 20965) dissolved in anhydrous ethanol, heated to boiling, input of sodium and to maintain refluxing. Sodium dissolved finished, the cooling of reactants, water dilution, the reaction mass distillation, so that distillate removal of ethanol, water and unreacted oxime, remnants of Chiang Kai-shek g amine hydrochloride that is crystallized, using alkali treatment. The availability was G amine and the yield was 60-73%.

Heptylamine Toxicity Data With Reference

1.		ipr-rat LDLo:75 mg/kg		FATOAO Farmakologiya i Toksikologiya (Moscow). 31 (1968),238.
2.		ipr-mus LD50:100 mg/kg		JAPMA8 Journal of the American Pharmaceutical Association, Scientific Edition. 30 (1941),623.

Heptylamine Consensus Reports

Reported in EPA TSCA Inventory.

Heptylamine Safety Profile

Poison by intraperitoneal route. A flammable liquid. When heated to decomposition it emits toxic vapors of NO_x.Safety information of Heptylamine (CAS NO.111-68-2):
Hazard Codes Corrosive C
Risk Statements
10 Flammable
34 Causes burns
Safety Statements
26 In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
36/37/39 Wear suitable protective clothing, gloves and eye/face protection
45 In case of accident or if you feel unwell, seek medical advice immediately (show label where possible)
RIDADR UN 2734 8/PG 2
WGK Germany 1
RTECS MK0600000
F 34
HazardClass 3
PackingGroup III

Heptylamine Standards and Recommendations

DOT Classification: 8; Label: Corrosive, Flammable Liquid (UN 2734); DOT Class: 3; Label: Flammable Liquid, Corrosive (UN 2733)

Product Name

1-Aminoheptane

Synthetic route

Heptylamine Chemical Properties

Heptylamine Uses

Heptylamine Production

Heptylamine Toxicity Data With Reference

Heptylamine Consensus Reports

Heptylamine Safety Profile

Heptylamine Standards and Recommendations

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