Potassium cyanide supplier

This product is a nationally controlled contraband, and the Lookchem platform doesn't provide relevant sales information.

Name
Potassium cyanide
EINECS 205-792-3
CAS No. 151-50-8
Article Data86
CAS DataBase
Density 1.00 g/mL at 20 °C
Solubility Soluble in water
Melting Point 634.5 °C
Formula KCN
Boiling Point 1625 °C
Molecular Weight 65.116
Flash Point 1625°C
Transport Information UN 1680 6.1/PG 1
Appearance White crystalline solid
Safety 7-28-29-45-60-61
Risk Codes 26/27/28-32-50/53
Molecular Structure
Hazard Symbols N, T+
Synonyms Potassiumcyanide (8CI);Cyanide of potassium;Hydrocyanic acid, potassium salt;Kalium cyanid;Potassium cyanide (K(CN));
PSA 23.79000
LogP 0.01678

Synthetic route

: 74-90-8
hydrogen cyanide

: 917-58-8
potassium ethoxide

: 151-50-8
potassium cyanide

: 74-90-8
hydrogen cyanide

: 151-50-8
potassium cyanide

Conditions

Conditions	Yield
With potassium hydroxide; ethanol

: 590-28-3
potassium cyanate

: 151-50-8
potassium cyanide

Conditions

Conditions	Yield
at 700℃;
at 900℃;

: 333-20-0
potassium thioacyanate

: 497-19-8
sodium carbonate

: 151-50-8
potassium cyanide

: 86-74-8
9H-carbazole

KOH: KOH

: 151-50-8
potassium cyanide

Conditions

Conditions	Yield
anschl. Gluehen;
anschl. Gluehen;

: 108-80-5
cyanuric acid

potassium: potassium

: 151-50-8
potassium cyanide

Conditions

Conditions	Yield
Schmelzen mit viel Kalium;

: N-(benzo[1,3]dioxol-5-yl-cyano-methyl)-glycin-ethyl ester

alcoholic KOH-solution: alcoholic KOH-solution

A: N-piperonylidene-glycine

B: 151-50-8
potassium cyanide

...Expand

: 99-11-6
citrazinic acid

potassium hydroxide: potassium hydroxide

A: 151-50-8
potassium cyanide

B: 144-62-7
oxalic acid

Conditions

Conditions	Yield
beim Schmelzen;

...Expand

: 859802-57-6
2,6-diethyl-5-methyl-3H-pyrimidin-4-one

potassium hydroxide: potassium hydroxide

A: 7664-41-7
ammonia

B: 151-50-8
potassium cyanide

C: 64-19-7
acetic acid

D: 802294-64-0
propionic acid

Conditions

Conditions	Yield
beim Schmelzen;

...Expand

: 69-93-2
uric Acid

potassium hydroxide: potassium hydroxide

A: 590-28-3
potassium cyanate

B: 151-50-8
potassium cyanide

C potassium carbonate: potassium carbonate

Conditions

Conditions	Yield
im bedeckten Tiegel;

...Expand

: 69-93-2
uric Acid

potassium hydroxide: potassium hydroxide

A: 7664-41-7
ammonia

B: 151-50-8
potassium cyanide

C: 583-52-8
potassium oxalate

D potassium carbonate: potassium carbonate

...Expand

: 556-64-9
methyl thiocyanate

alcoholic KOH-solution: alcoholic KOH-solution

A: 624-92-0
Dimethyldisulphide

B: 7664-41-7
ammonia

C: 151-50-8
potassium cyanide

D potassium carbonate: potassium carbonate

...Expand

: 19159-68-3
dipicryl-diazene

diluted KOH-solution: diluted KOH-solution

A: 151-50-8
potassium cyanide

B: 88-89-1
2,4,6-Trinitrophenol

C: 68683-32-9
2,2',4,4',6,6'-hexanitrohydrazobenzene

D potassium nitrite: potassium nitrite

...Expand

: 60-29-7
diethyl ether

: 506-78-5
cyanogen iodide

KOH: KOH

: 151-50-8
potassium cyanide

...Expand

: 506-68-3
bromocyane

: 64-17-5
ethanol

KOH: KOH

: 151-50-8
potassium cyanide

...Expand

: 506-78-5
cyanogen iodide

: 64-17-5
ethanol

KOH: KOH

: 151-50-8
potassium cyanide

...Expand

: 60-29-7
diethyl ether

: 506-68-3
bromocyane

: 67-66-3
chloroform

KOH: KOH

: 151-50-8
potassium cyanide

...Expand

: 506-78-5
cyanogen iodide

: 67-66-3
chloroform

KOH: KOH

: 151-50-8
potassium cyanide

...Expand

: 506-68-3
bromocyane

: 7732-18-5
water

KOH: KOH

: 151-50-8
potassium cyanide

...Expand

: 506-78-5
cyanogen iodide

: 7732-18-5
water

KOH: KOH

: 151-50-8
potassium cyanide

...Expand

: 460-19-5
ethanedinitrile

potassium: potassium

: 151-50-8
potassium cyanide

: 460-19-5
ethanedinitrile

potassium carbonate: potassium carbonate

A: 590-28-3
potassium cyanate

B: 151-50-8
potassium cyanide

Conditions

Conditions	Yield
in der Rotglut;

...Expand

: 542-90-5
ethyl isothiocyanate

aqueous KOH-solution: aqueous KOH-solution

A: 110-81-6
Diethyl disulfide

B: 590-28-3
potassium cyanate

C: 151-50-8
potassium cyanide

Conditions

Conditions	Yield
at 100℃; im zugeschmolzenen Rohr;

...Expand

: 14752-58-0
trichloroacetonitrile

concentrated KOH-solution: concentrated KOH-solution

A: 7664-41-7
ammonia

B: 151-50-8
potassium cyanide

...Expand

: 13369-04-5
Cyan-imidoameisensaeureethylester

alcoholic potash: alcoholic potash

A: 151-50-8
potassium cyanide

B: potassium fulminate

...Expand

: 460-19-5
ethanedinitrile

aqueous KOH-solution: aqueous KOH-solution

A: 151-50-8
potassium cyanide

B: potassium fulminate

...Expand

: 624-79-3
ethyl isocyanide

: potassium amide

A: 151-50-8
potassium cyanide

B: 75-04-7
ethylamine

...Expand

: 624-79-3
ethyl isocyanide

: potassium amide

liquid.ammonia: liquid.ammonia

A: 151-50-8
potassium cyanide

B: 75-04-7
ethylamine

Conditions

Conditions	Yield
at 80℃;

...Expand

: 460-19-5
ethanedinitrile

aqueous KOH-solution: aqueous KOH-solution

A: 590-28-3
potassium cyanate

B: 7664-41-7
ammonia

C: 151-50-8
potassium cyanide

D azulminic acid: azulminic acid

Conditions

Conditions	Yield
Produkt5: CO2;

...Expand

: 460-19-5
ethanedinitrile

K2CO3: K2CO3

A: 590-28-3
potassium cyanate

B: 124-38-9
carbon dioxide

C: 151-50-8
potassium cyanide

D paracyan: paracyan

Conditions

Conditions	Yield
at 190 - 370℃; Produkt 5: Stickstoff;

...Expand

: 111-83-1
1-bromo-octane

: 151-50-8
potassium cyanide

: 2243-27-8
nonanonitrile

Conditions

Conditions	Yield
Sucrose-ethyleneoxide adducts In acetonitrile at 83℃; for 24h; Product distribution; further catalysts: PEG, DB18K6; further objects of study: phase-transfer catalysis; further solvents: toluene/H2O;	100%
tetraoctyl ammonium bromide In water; toluene at 90℃; for 24h; Product distribution; other phase-transfer catalysts, time;	99%
tetraoctyl ammonium bromide In water; toluene at 90℃; for 24h;	99%

: 151-50-8
potassium cyanide

: 98-86-2
acetophenone

: 20102-12-9
2-hydroxy-2-phenylpropionitrile

Conditions

Conditions	Yield
Stage #1: potassium cyanide; acetophenone With 18-crown-6 ether In dichloromethane at 20℃; for 4h; Stage #2: With hydrogenchloride In tetrahydrofuran; dichloromethane at 0 - 20℃; for 2h;	100%
Stage #1: potassium cyanide; acetophenone With tetrachlorosilane In acetonitrile at 60 - 70℃; for 5h; Stage #2: With sodium hydrogencarbonate In water; acetonitrile Further stages.;	82%
With hydrogenchloride

: 151-50-8
potassium cyanide

: 402-23-3
1-bromomethyl-3-trifluoromethylbenzene

: 2338-76-3
3-trifluoromethylphenylacetonitrile

Conditions

Conditions	Yield
In ethanol; water for 1.5h; Heating / reflux;	100%
In dimethyl sulfoxide

: 500-22-1
3-pyridinecarboxaldehyde

: 151-50-8
potassium cyanide

: 17604-74-9
2-hydroxy-2-(pyridin-3-yl)acetonitrile

Conditions

Conditions	Yield
With water; acetic acid at 5 - 10℃; for 2h;	100%
With hydrogenchloride
With acetic acid In water for 18h; Ambient temperature;

: 75-77-4
chloro-trimethyl-silane

: 3900-45-6
6-methoxy-2-acetylnaphthalene

: 151-50-8
potassium cyanide

: 107727-73-1
2-(6-methoxy-2-naphthyl)-2-(trimethylsilyloxy)propiononitrile

Conditions

Conditions	Yield
In N,N-dimethyl-formamide at 60℃; for 13.5h;	100%

...Expand

: 71629-66-8
(+)-<(1S,2S)-1-Hydroxy-2-methyl-3-oxo-cyclopent-2-yl>-essigsaeure-γ-lacton

: 151-50-8
potassium cyanide

: 98926-41-1
(1S,2S)-6-Cyano-6-hydroxy-5-methyl-2-oxa-bicyclo<3.3.0>octan-3-on

Conditions

Conditions	Yield
In water; acetic acid at 5℃; for 20h;	100%

: 124-13-0
Octanal

: 593-51-1
methylamine hydrochloride

: 151-50-8
potassium cyanide

: 112101-12-9
2-Methylamino-nonanenitrile

Conditions

Conditions	Yield
With aluminum oxide In acetonitrile at 50℃; for 22h; ultrasound;	100%

...Expand

: 51991-03-8
5-anti-Chloro-6-syn-cyanobicyclo<2.1.1>hexene

: 151-50-8
potassium cyanide

: 72431-16-4
endo,endo-3,5-Dicyanotricyclo<2.2.0.02.6>hexane

Conditions

Conditions	Yield
In water; acetonitrile for 30h; Ambient temperature;	100%

: 841-95-2
9,10-dimethoxy-1,3,4,6,7,11b-hexahydro-2H-benzo[a]quinolizin-2-one

: 151-50-8
potassium cyanide

: 133308-74-4
2-Amino-9,10-dimethoxy-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinoline-2-carbonitrile

Conditions

Conditions	Yield
With ammonia; acetic acid In water at 40℃; for 25h; Irradiation; irrad. with ultrasound;	100%

: 151-50-8
potassium cyanide

: 1-Chloromethyl-7-methoxy-1,4,4-trimethyl-isothiochroman

: 128276-86-8
7-methoxy-1,4,4-trimethylisothiochroman-1-ylacetonitril

Conditions

Conditions	Yield
In ethanol; water for 3h; Heating;	100%

: 151-50-8
potassium cyanide

: 100-39-0
benzyl bromide

: 140-29-4
phenylacetonitrile

Conditions

Conditions	Yield
Sucrose-ethyleneoxide adducts In acetonitrile at 20℃; for 8h; Product distribution; further catalysts: PEG, DB18K6; further objects of study: phase-transfer catalysis; further solvents: toluene/H2O;	100%
With water; Aliquat 336 for 2h; Ambient temperature;	97%
With poly(ethylene glycol)-supported tetrabutylamminium bromide In water at 25℃; for 2h; Substitution;	97%

: 151-50-8
potassium cyanide

: 142-04-1
aniline hydrochloride

: 459-57-4
4-fluorobenzaldehyde

: 124573-71-3
2-(4-fluorophenyl)-2-(phenylamino) acetonitrile

Conditions

Conditions	Yield
In ethanol; water 1.) 1 h cooling; 2.) 20 h room temperature;	100%

...Expand

: 151-50-8
potassium cyanide

: <5-(Diphenylmethylen)-1,3-cyclopentadien-1-yl>dimethylsulfonium-perchlorat

: 1-(Cyandiphenylmethyl)-2-(dimethylsulfonio)cyclopentadienid

Conditions

Conditions	Yield
In methanol at 0℃; for 0.25h;	100%

: 151-50-8
potassium cyanide

: <5-(Diphenylmethylen)-1,3-cyclopentadien-1-yl>diphenylsulfonium-perchlorat

: 1-(Cyandiphenylmethyl)-2-(diphenylsulfonio)cyclopentadienid

Conditions

Conditions	Yield
In methanol at 0℃; for 0.25h;	100%

: 151-50-8
potassium cyanide

: <5-(Diphenylmethylen)-1,3-cyclopentadien-1-yl>bis(4-methylphenyl)sulfonium-perchlorat

: 1--2-(cyandiphenylmethyl)cyclopentadienid

Conditions

Conditions	Yield
In methanol at 0℃; for 0.25h;	100%

: 151-50-8
potassium cyanide

: 104700-37-0
ethyl [L-(trans)]-4-[(t-butoxycarbonyl)amino]-2-pentenoate

: (S)-4-tert-Butoxycarbonylamino-3-cyano-pentanoic acid ethyl ester

Conditions

Conditions	Yield
With 18-crown-6 ether In acetonitrile for 24h; Ambient temperature;	100%

: 151-50-8
potassium cyanide

: 161363-80-0
2-Benzyl-3-(bromomethyl)-1,4-dimethoxynaphthalene

: 161363-81-1
2-Benzyl-3-(cyanomethyl)-1,4-dimethoxynaphthalene

Conditions

Conditions	Yield
In 1,4-dioxane; water for 10h; Heating;	100%

: 151-50-8
potassium cyanide

: 60211-89-4, 63616-13-7, 93424-19-2
trans-1-iodo-2-isothiocyanatocyclohexane

: 77469-22-8
2-cyano-cis-3a,4,5,6,7,7a-hexahydrobenzothiazole

Conditions

Conditions	Yield
With 18-crown-6 ether In chloroform; water for 92h; Heating;	100%

: 151-50-8
potassium cyanide

: 114200-84-9
4'-(chloromethyl)dispirobis<1,3>dioxole-6',1''-cyclohexane>

: 114200-85-0
dispirobis<1,3>dioxole-6',1''-cyclohexane>-4'-acetonitrile

Conditions

Conditions	Yield
With 18-crown-6 ether In acetonitrile for 5h; Heating;	100%

: 151-50-8
potassium cyanide

: 120667-42-7
diethyl <<3-(bromomethyl)phenyl>methyl>phosphonate

: 140151-14-0
diethyl <<3-(cyanomethyl)phenyl>methyl>phosphonate

Conditions

Conditions	Yield
With sodium iodide In water; acetone at 50℃; for 48h;	100%

: 151-50-8
potassium cyanide

: 108228-81-5
4-(diethoxyphosphorylmethyl)-1-bromomethyl-phenyl

: 135335-15-8
diethyl <<4-(cyanomethyl)phenyl>methyl>phosphonate

Conditions

Conditions	Yield
With sodium iodide In water; acetone at 50℃; for 48h;	100%

: 151-50-8
potassium cyanide

: 3-(2,6-Dimethylphenyl)-4-methyl-5-acetyl-2-imino-thiazolin Hydrobromid

: 2-Aminocarbonylimino-3-(2,6-dimethylphenyl)-4-methyl-5-acetyl-thiazolin

Conditions

Conditions	Yield
In water	100%

: 151-50-8
potassium cyanide

: <5-(Diphenylmethylen)-1,3-cyclopentadien-1-yl>methylphenylsulfonium-perchlorat

: 1-(Cyandiphenylmethyl)-2-(methylphenylsulfonio)cyclopentadienid

Conditions

Conditions	Yield
In methanol at 0℃; for 0.25h;	100%

: 151-50-8
potassium cyanide

: ethyl 8,9-bis(4-methoxyphenyl)-10,10-dimethyl-5-oxotricyclo<5.2.1.02,6>deca-3,8-diene-2-carboxylate

: (3aS,4R,7S,7aR)-3-Cyano-5,6-bis-(4-methoxy-phenyl)-8,8-dimethyl-1-oxo-1,2,3,4,7,7a-hexahydro-4,7-methano-indene-3a-carboxylic acid ethyl ester

Conditions

Conditions	Yield
With ammonium chloride In water; N,N-dimethyl-formamide at 100℃; for 4.5h;	100%

: 151-50-8
potassium cyanide

: 75-07-0
acetaldehyde

: 60-15-1, 156-34-3, 51-64-9, 300-62-9
2-amino-1-phenylpropane

: 3535-04-4
2-<(1-methyl-2-phenylethyl)amino>propanenitrile

Conditions

Conditions	Yield
With sodium hydrogensulfite In methanol; water Ambient temperature;	100%

...Expand

: 593-51-1
methylamine hydrochloride

: 151-50-8
potassium cyanide

: 98-86-2
acetophenone

: 112101-15-2
2-methylamino-2-phenyl-propionitrile

Conditions

Conditions	Yield
With aluminum oxide In acetonitrile at 50℃; for 24h; ultrasound;	100%

...Expand

: 151-50-8
potassium cyanide

: 591-31-1
3-methoxy-benzaldehyde

: 53313-94-3
m-methoxymandelonitrile

Conditions

Conditions	Yield
Stage #1: 3-methoxy-benzaldehyde With hydrogenchloride; sodium sulfite In tetrahydrofuran; water at 20℃; for 0.166667h; Stage #2: potassium cyanide In tetrahydrofuran; water for 0.5h;	100%
With sodium hydrogensulfite 1) H2O, 40 deg C, 0.5 h, 2) H2O, 0 deg C, 1 h; Multistep reaction;
With acetic acid In water
With hydrogenchloride; sodium sulfite In tetrahydrofuran at 20℃; for 0.5h;

: 50-00-0
formaldehyd

: 151-50-8
potassium cyanide

: 103-67-3
benzyl-methyl-amine

: 14321-25-6
(N-benzyl-N-methylamino)acetonitrile

Conditions

Conditions	Yield
With hydrogenchloride for 16h; Ambient temperature;	100%

...Expand

: 151-50-8
potassium cyanide

: (1S,5R,6R,7R)-1-((4S,5R)-4-Acetoxy-5-methyl-3-methylene-6-phenyl-hexyl)-6-((E)-(4S,6S)-4,6-dimethyl-oct-2-enoyloxy)-7-hydroxy-4-oxo-2,8-dioxa-bicyclo[3.2.1]octane-5-carboxylic acid

: (1S,5R,6R,7R)-1-((4S,5R)-4-Acetoxy-5-methyl-3-methylene-6-phenyl-hexyl)-4-cyano-6-((E)-(4S,6S)-4,6-dimethyl-oct-2-enoyloxy)-4,7-dihydroxy-2,8-dioxa-bicyclo[3.2.1]octane-5-carboxylic acid

Conditions

Conditions	Yield
With acetic acid In methanol; isopropyl alcohol	100%

: 52421-93-9
(2Z)-3-methyl-2-penten-4-ynal

: 151-50-8
potassium cyanide

: (Z)-1-cyano-3-methylpent-2-en-4-yn-1-ol

Conditions

Conditions	Yield
With hydrogenchloride In diethyl ether; water 30 min, 0 deg C; 2 h, 20 deg C;	100%

Potassium cyanide Specification

The IUPAC name of Potassium cyanide is potassium cyanide. With the CAS registry number 151-50-8, it is also named as Hydrocyanic acid, potassium salt. The product's categories are Inorganics; ACS Grade; Essential Chemicals; Routine Reagents; Masking AgentsAnalytical Reagents for General Use; Complexometric Titration (IDRANAL); O-P, Puriss p.a. ACS; Puriss p.a. ACS; Titration; Masking Agents; O-P, Puriss p.a.; Puriss p.a., and the other registry numbers are 133708-36-8; 15745-74-1; 60195-52-0. Besides, it is white granular powder or crystals, which should be sealed in a cool and dry warehouse. In addition, its molecular formula is CKN and molecular weight is 65.12.

The other characteristics of this product can be summarized as: (1)EINECS: 205-792-3; (2)H-Bond Donor: 0; (3)H-Bond Acceptor: 2; (4)Rotatable Bond Count: 0; (5)Exact Mass: 64.966781; (6)MonoIsotopic Mass: 64.966781; (7)Topological Polar Surface Area: 23.8; (8)Heavy Atom Count: 3; (9)Complexity: 12.8; (10)Density: 1.52 g/cm³; (11)Melting point: 634.5 °C; (12)Boiling point: 1625 °C; (13)Flash Point: 1625 °C; (14)Solubility in water: 71.6 g/100 ml (25 °C).

Preparation of Potassium cyanide: this chemical can be prepared by the treatment of Hydrogen cyanide with Potassium hydroxide:
HCN + KOH → KCN + H₂O

Uses of Potassium cyanide: it is widely used in organic synthesis for the preparation of nitriles and carboxylic acids. It is also used in electroplating, such as jewelry for chemical gilding and buffing. And this product has been used as a killing agent in collecting jars by entomologists. Additionally, this chemical can form water-soluble salts from gold metal in the presence of air in gold mining:
4 Au + 8 KCN + O₂+ 2 H₂O → 4 K[Au(CN)₂] + 4 KOH

When you are using this chemical, please be cautious about it as the following: it is very toxic by inhalation, in contact with skin and if swallowed. And it would liberate very toxic gas in contact with acid. Please keep container tightly closed and do not empty into drains. After contact with skin, you should wash immediately with plenty of soap-suds. Moreover, it is very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) And this material and its container must be disposed of as hazardous waste. Please avoid release to the environment and refer to special instructions / safety data sheets.

People can use the following data to convert to the molecule structure.
(1)Canonical SMILES: [C-]#N.[K+]
(2)InChI: InChI=1S/CN.K/c1-2;/q-1;+1
(3)InChIKey: NNFCIKHAZHQZJG-UHFFFAOYSA-N

The toxicity data is as follows:

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Effect	Source
cat	LD50	intravenous	2200ug/kg (2.2mg/kg)		Proceedings of the Society for Experimental Biology and Medicine. Vol. 35, Pg. 316, 1936.
dog	LD50	subcutaneous	6mg/kg (6mg/kg)	BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD	Archiv fuer Toxikologie. Vol. 21, Pg. 89, 1965.
dog	LDLo	intravenous	5mg/kg (5mg/kg)		"Drug Dosages in Laboratory Animals - A Handbook," Rev. ed., Barnes, C.D., and L.G. Eltherington, Berkeley, Univ. of California Press, 1973Vol. -, Pg. 209, 1973.
frog	LDLo	subcutaneous	60mg/kg (60mg/kg)		Archives Internationales de Pharmacodynamie et de Therapie. Vol. 3, Pg. 77, 1897.
guinea pig	LDLo	intraarterial	5mg/kg (5mg/kg)		Naunyn-Schmiedeberg's Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 131, Pg. 171, 1928.
guinea pig	LDLo	intraperitoneal	8mg/kg (8mg/kg)		Comptes Rendus des Seances de la Societe de Biologie et de Ses Filiales. Vol. 96, Pg. 202, 1927.
guinea pig	LDLo	intravenous	5mg/kg (5mg/kg)		Naunyn-Schmiedeberg's Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 131, Pg. 171, 1928.
guinea pig	LDLo	subcutaneous	8mg/kg (8mg/kg)		Comptes Rendus des Seances de la Societe de Biologie et de Ses Filiales. Vol. 96, Pg. 202, 1927.
human	LDLo	oral	2857ug/kg (2.857mg/kg)		"Toxicology of Drugs and Chemicals," Deichmann, W.B., New York, Academic Press, Inc., 1969Vol. -, Pg. 191, 1969.
man	TDLo	oral	13699ug/kg (13.699mg/kg)	BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD BEHAVIORAL: COMA	Journal of Toxicology, Clinical Toxicology. Vol. 25, Pg. 121, 1987.
mouse	LD50	intraperitoneal	5991ug/kg (5.991mg/kg)		Pesticide Biochemistry and Physiology. Vol. 2, Pg. 95, 1972.
mouse	LD50	intravenous	2600ug/kg (2.6mg/kg)	PERIPHERAL NERVE AND SENSATION: FLACCID PARALYSIS WITHOUT ANESTHESIA (USUALLY NEUROMUSCULAR BLOCKAGE) LUNGS, THORAX, OR RESPIRATION: RESPIRATORY STIMULATION BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD	Japanese Journal of Pharmacology. Vol. 3, Pg. 99, 1954.
mouse	LD50	oral	8500ug/kg (8.5mg/kg)		Journal of Pharmacology and Experimental Therapeutics. Vol. 161, Pg. 163, 1968.
mouse	LD50	subcutaneous	6500ug/kg (6.5mg/kg)		Nippon Yakurigaku Zasshi. Japanese Journal of Pharmacology. Vol. 54, Pg. 1057, 1958.
pigeon	LD50	intramuscular	4mg/kg (4mg/kg)		Japanese Journal of Pharmacology. Vol. 3, Pg. 99, 1954.
rabbit	LD50	intramuscular	3256ug/kg (3.256mg/kg)		Journal of the American College of Toxicology. Vol. 1(3), Pg. 120, 1982.
rabbit	LD50	intraperitoneal	3972ug/kg (3.972mg/kg)	BLOOD: OTHER CHANGES	Toxicologist. Vol. 3, Pg. 64, 1983.
rabbit	LD50	ocular	7870ug/kg (7.87mg/kg)	SENSE ORGANS AND SPECIAL SENSES: OTHER: EYE BEHAVIORAL: ATAXIA LUNGS, THORAX, OR RESPIRATION: RESPIRATORY STIMULATION	Journal of Toxicology, Cutaneous and Ocular Toxicology. Vol. 2, Pg. 119, 1983.
rabbit	LD50	oral	5mg/kg (5mg/kg)		"Drug Dosages in Laboratory Animals - A Handbook," Rev. ed., Barnes, C.D., and L.G. Eltherington, Berkeley, Univ. of California Press, 1973Vol. -, Pg. 209, 1973.
rabbit	LD50	subcutaneous	4mg/kg (4mg/kg)	LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES	Japanese Journal of Pharmacology. Vol. 3, Pg. 99, 1954.
rat	LD50	intraperitoneal	4mg/kg (4mg/kg)	LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES	Journal of Applied Physiology. Vol. 32, Pg. 315, 1972.
rat	LD50	intravenous	3600ug/kg (3.6mg/kg)	BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD LUNGS, THORAX, OR RESPIRATION: DYSPNEA	Drug Development Research. Vol. 5, Pg. 225, 1985.
rat	LD50	oral	5mg/kg (5mg/kg)		Archives of Toxicology. Vol. 54, Pg. 275, 1983.
rat	LD50	subcutaneous	7814ug/kg (7.814mg/kg)		Archives of Toxicology, Supplement. Vol. 14, Pg. 231, 1991.
rat	LDLo	intramuscular	8mg/kg (8mg/kg)		"Drug Dosages in Laboratory Animals - A Handbook," Rev. ed., Barnes, C.D., and L.G. Eltherington, Berkeley, Univ. of California Press, 1973Vol. -, Pg. 209, 1973.
women	TDLo	oral	100mg/kg (100mg/kg)	BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD CARDIAC: PULSE RATE INCREASE WITHOUT FALL IN BP VASCULAR: BP LOWERING NOT CHARACTERIZED IN AUTONOMIC SECTION	American Journal of Emergency Medicine. Vol. 1, Pg. 94, 1983.

Product Name

Potassium cyanide

Synthetic route

Potassium cyanide Specification

Related Products

Hot Products