Hydrogen Cyanide
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Basic Info
Common Name | Hydrogen Cyanide(F03376) |
2D Structure | |
Description | Hydrogen cyanide (with the historical common name of Prussic acid) is a chemical compound with chemical formula HCN. It is a colorless, extremely poisonous liquid that boils slightly above room temperature at 26 C (79ЎF). A hydrogen cyanide concentration of 300 mg/m3 in air will kill a human within 10Р60 minutes.[38] A hydrogen cyanide concentration of 3500 ppm (about 3200 mg/m3) will kill a human in about 1 minute.[38] The toxicity is caused by the cyanide ion, which halts cellular respiration by acting as a non-competitive inhibitor for an enzyme in mitochondria called cytochrome c oxidase. |
FRCD ID | F03376 |
CAS Number | 74-90-8 |
PubChem CID | 768 |
Formula | CHN |
IUPAC Name | formonitrile |
InChI Key | LELOWRISYMNNSU-UHFFFAOYSA-N |
InChI | InChI=1S/CHN/c1-2/h1H |
Canonical SMILES | C#N |
Isomeric SMILES | C#N |
Wikipedia | Hydrogen Cyanide |
Synonyms | Prussic acid hydrogen cyanide hydrocyanic acid Formonitrile Cyanwasserstoff Blausaeure Formic anammonide Zyklon B Zaclondiscoids Cyclon |
Classifies | Pollutant Pesticide |
Update Date | Nov 13, 2018 17:07 |
Chemical Taxonomy
Kingdom | Organic compounds |
Superclass | Organic nitrogen compounds |
Class | Organonitrogen compounds |
Subclass | Organic cyanides |
Intermediate Tree Nodes | Not available |
Direct Parent | Nitriles |
Alternative Parents | |
Molecular Framework | Aliphatic acyclic compounds |
Substituents | Carbonitrile - Organopnictogen compound - Hydrocarbon derivative - Aliphatic acyclic compound |
Description | This compound belongs to the class of organic compounds known as nitriles. These are compounds having the structure RC#N; thus C-substituted derivatives of hydrocyanic acid, HC#N. |
Properties
Property Name | Property Value |
---|---|
Molecular Weight | 27.026 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 1 |
Rotatable Bond Count | 0 |
Complexity | 10 |
Monoisotopic Mass | 27.011 |
Exact Mass | 27.011 |
XLogP | 0.1 |
Formal Charge | 0 |
Heavy Atom Count | 2 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Isotope Atom Count | 0 |
Covalently-Bonded Unit Count | 1 |
MRLs
Food | Product Code | Country | MRLs | Application Date | Notes |
---|---|---|---|---|---|
Other Cereals Do Not Include Rice | Britain | 15mg/kg | |||
Rice | Britain | 15mg/kg | |||
Millet | Britain | 15mg/kg | |||
Buckwheat | Britain | 15mg/kg | |||
Maize | Britain | 15mg/kg | |||
Triticale | Britain | 15mg/kg | |||
Oats | Britain | 15mg/kg | |||
Sorghum | Britain | 15mg/kg | |||
Barley | Britain | 15mg/kg | |||
Rye | Britain | 15mg/kg | |||
Wheat | Britain | 15mg/kg | |||
Hop | Japan | 1ppm | |||
Cacao Beans | Japan | 30ppm | |||
Coffee Beans | Japan | 1ppm | |||
Tea | Japan | 1ppm | |||
Grapefruit | Japan | 50ppm | |||
Orange(Including Navel Orange) | Japan | 50ppm | |||
Lemon | Japan | 50ppm | |||
Sugarcane | Japan | 1ppm | |||
Sugar Beet | Japan | 1ppm |
References
Title | Journal | Date | Pubmed ID |
---|---|---|---|
Cyanogenesis in Arthropods: From Chemical Warfare to Nuptial Gifts. | Insects | 2018 May 3 | 29751568 |
Biosynthesis and regulation of cyanogenic glycoside production in forage plants. | Appl Microbiol Biotechnol | 2018 Jan | 29022076 |
Thermal behavior of inosine 5'-monophosphate in acidic form and as alkali andalkaline earth salts. | Food Chem | 2018 Aug 30 | 29655723 |
Antinutritional factors and hypocholesterolemic effect of wild apricot kernel (Prunus armeniaca L.) as affected by detoxification. | Food Funct | 2018 Apr 25 | 29644368 |
A socio-scientific analysis of the environmental and health benefits as well aspotential risks of cassava production and consumption. | Environ Sci Pollut Res Int | 2017 Feb | 28013470 |
<i>Bacillus</i>: A Biological Tool for Crop Improvement through Bio-Molecular Changes in Adverse Environments. | Front Physiol | 2017 | 28932199 |
An <i>In vitro</i> Study of Bio-Control and Plant Growth Promotion Potential of Salicaceae Endophytes. | Front Microbiol | 2017 | 28348550 |
In vitro assessment of the genotoxic and cytotoxic effects of boiled juice (tucupi) from Manihot esculenta Crantz roots. | Genet Mol Res | 2016 Oct 5 | 27808379 |
Application of the Prunus spp. Cyanide Seed Defense System onto Wheat: ReducedInsect Feeding and Field Growth Tests. | J Agric Food Chem | 2016 May 11 | 27119432 |
Lepidopteran defence droplets - a composite physical and chemical weapon against potential predators. | Sci Rep | 2016 Mar 4 | 26940001 |
Selenium in Cattle: A Review. | Molecules | 2016 Apr 23 | 27120589 |
Characterisation of Development and Electrophysiological Mechanisms Underlying Rhythmicity of the Avian Lymph Heart. | PLoS One | 2016 | 27930653 |
Zinc-Induced Effects on Osteoclastogenesis Involves Activation ofHyperpolarization-Activated Cyclic Nucleotide Modulated Channels via Changes inMembrane Potential. | J Bone Miner Res | 2015 Sep | 25762086 |
Detection and characterization of broad-spectrum antipathogen activity of novelrhizobacterial isolates and suppression of Fusarium crown and root rot disease oftomato. | J Appl Microbiol | 2015 Mar | 25512025 |
Salt tolerant SUV3 overexpressing transgenic rice plants conserve physicochemical properties and microbial communities of rhizosphere. | Chemosphere | 2015 Jan | 25303666 |
Regulation of GacA in Pseudomonas chlororaphis Strains Shows a Niche Specificity. | PLoS One | 2015 | 26379125 |
Variation in cyanogenic glycosides across populations of wild lima beans (Phaseolus lunatus) has no apparent effect on bruchid beetle performance. | J Chem Ecol | 2014 May | 24863488 |
[Health risks from pest control products]. | Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz | 2014 May | 24781915 |
Transcriptional regulation of de novo biosynthesis of cyanogenic glucosides throughout the life-cycle of the burnet moth Zygaena filipendulae (Lepidoptera). | Insect Biochem Mol Biol | 2014 Jun | 24727026 |
Chemical defense balanced by sequestration and de novo biosynthesis in a lepidopteran specialist. | PLoS One | 2014 | 25299618 |