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 |