hydrogen cyanide

chemical compound

External resources

CAS Registry Number
ZVG number
HCIS ID
DSSTOX compound identifier
Encyclopædia Britannica Online ID
science/hydrogen-cyanide

subject named as: hydrogen cyanide

science/hydrocyanic-acid

subject named as: hydrocyanic acid

ChEMBL ID
Gran Enciclopèdia Catalana ID
Nikkaji ID
Human Metabolome Database ID
OmegaWiki Defined Meaning
MeSH tree code
RTECS number
MW6825000
ECHA Substance Infocard ID
CAMEO Chemicals ID
NALT ID
Encyclopedia of China (Third Edition) ID
J9U ID
Freebase ಐಡಿ
CA PROP 65 ID
Reaxys registry number
1718793[]
PubChem CID
UN number
UniChem compound ID
KEGG ID
YSO ID
4368[೧೨]

subject named as: syaanivety, cyanväte, hydrocyanic acid

SPLASH
PesticideInfo chemical ID
GND ಐಡಿ
BNCF Thesaurus ID
ChemSpider ID
OpenAlex ID
DSSTox substance ID
InChIKey
Cannabis Database ID
ChEBI ID
18407[][೧೯]

mapping relation type: exact match

MeSH descriptor ID
D006856

subject named as: Hydrogen Cyanide

J-GLOBAL ID
InChI
UNII
Gran Enciclopèdia Catalana ID (former scheme)
Lex ID
Bibliothèque nationale de France ID
122825291[೨೦]

subject named as: Acide cyanhydrique

KBpedia ID
KNApSAcK ID
Microsoft Academic ID
Library of Congress authority ID
OSHA Occupational Chemical Database ID
Encyclopædia Universalis ID
EC number
NL CR AUT ID
ph269131

subject named as: kyanovodík

AHECC 2017 ID
28111200
Great Russian Encyclopedia portal ID
RxNorm ID
HSDB ID

ಉದಾಹರಣೆಗೆ

type of chemical entity

ಉಪವರ್ಗ

monoprotic acid
nitrile
carbon acid

ಇದರ ಭಾಗವಾಗಿದೆ

thiosulfate sulfurtransferase activity[೨೪]
1-aminocyclopropane-1-carboxylate oxidase activity[೨೪]
cyanide hydratase activity[೨೪]
cyanocobalamin reductase (cyanide-eliminating) activity[೨೪]
mandelonitrile lyase activity[೨೪]
L-3-cyanoalanine synthase activity[೨೪]
hydroxymandelonitrile lyase activity[೨೪]
glycine dehydrogenase (cyanide-forming) activity[೨೪]
(2R)-2-hydroxy-2-methylbutanenitrile lyase activity[೨೪]
acetone-cyanohydrin acetone-lyase (cyanide-forming) activity[೨೫]
aromatic (S)-hydroxynitrile lyase activity[೨೫]
cyanide metabolic process[೨೬]

subject has role: participant

cyanide catabolic process[೨೬]

subject has role: reactant

cyanide biosynthetic process[೨೬]

subject has role: product

response to cyanide[೨೬]

subject has role: reactant

cellular response to cyanide[೨೬]

subject has role: reactant

chemical structure

mass

೨೭.೦೧೧ dalton[೧೦]

associated hazard

hydrogen cyanide exposure

has effect

hydrogen cyanide exposure[೨೭]

conjugate acid

protonated hydrogen cyanide

conjugate base

cyanide anion

tautomer of

hydrogen isocyanide[೨೯]

chemical formula

canonical SMILES

[H+].[C-]#N

ionization energy

೧೩.೬±೦.೧ electronvolt[೨೭]

series ordinal: 1

೧೩.೬೦ electronvolt[೩೦]

series ordinal: 1

electric dipole moment

೨.೯೮ debye
೨.೯೮೪ debye[೩೦]

density

೦.೦೦೦೬೭೧ gram per cubic centimetre[೩೧]

temperature: ೨೦±೧ degree Celsius

phase of matter: ಅನಿಲ

melting point

೭±೧ ಫಾಹ್ರೆನ್ಹೈಟ್[೨೭]
−೧೩.೪ degree Celsius[೩೦]

boiling point

೭೮±೧ ಫಾಹ್ರೆನ್ಹೈಟ್[೨೭]

under pressure: ೭೬೦±೧ torr

೨೬ degree Celsius[೩೦]

under pressure: ೧೦೧.೩೨೫ kilopascal

dynamic viscosity

೦.೨೦೧ poiseuille

vapor pressure

೬೩೦±೧ millimetre of mercury[೨೭]

temperature: ೬೮±೧ ಫಾಹ್ರೆನ್ಹೈಟ್

pKa

೯.೨೧

refractive index

೧.೨೬೭೫

flash point

−೧೭.೮ degree Celsius

lower flammable limit

೫.೬±೦.೧ volume percent[೨೭]

upper flammable limit

೪೦±೧ volume percent[೨೭]

safety classification and labelling

NFPA 704: Standard System for the Identification of the Hazards of Materials for Emergency Response[೩೨]

NFPA Special: no value

NFPA Health: 4

NFPA Fire: 4

NFPA Instability: 1

Globally Harmonized System of Classification and Labelling of Chemicals (GHS)

GHS hazard pictogram: GHS02: flame, GHS06: skull and crossbones, GHS08: health hazard, GHS09: environment

GHS signal word: danger

NIOSH Pocket Guide ID

0333

short-term exposure limit

೫±೧ milligram per cubic metre[೨೭]

route of administration: skin absorption

applies to jurisdiction: no value

ಅವಧಿ: ೧೫±೧ ನಿಮಿಷ

time-weighted average exposure limit

೧೧±೧ milligram per cubic metre[೨೭]

route of administration: skin absorption

ಅವಧಿ: ೮±೧ ಘಂಟೆ

immediately dangerous to life or health

೫೫±೧ milligram per cubic metre[೨೭]

found in taxon

Nicotiana tabacum[೩೩]
Aronia melanocarpa[೩೪]
Eucalyptus cladocalyx[೩೫]
Mucuna curranii[೩೮]
Vigna umbellata[೩೮]
Canavalia ensiformis[೩೮]
Canavalia gladiata[೩೮]
Passiflora capsularis[೩೯]
Trifolium repens[೪೦]
ಬಾದಾಮಿ[೪೧]
Prunus armeniaca[೪೧]
Homo sapiens[೪೨]
Spongiidae[೪೪]
Canavalia africana[೩೮]
Trifolium semipilosum[೪೦]
Clostridium pasteurianum[೪೫]
Prunus avium[೪೧]

described by source

Armenian Soviet Encyclopedia
Encyclopædia Britannica 11th edition

statement is subject of: 1911 Encyclopædia Britannica/Prussic Acid

has characteristic

bitterness[೪೬]
Class IA flammable liquid[೨೭]

subject has role

chemical warfare agent[೪೭]
gas chamber[೪೮]
primary metabolite[೪೯]

on focus list of Wikimedia project

Wikiproject Nuremberg Trials

ಭಾಗವನ್ನು ಹೊಂದಿದೆ

ಕಾಮನ್ಸ್ ವರ್ಗ

Hydrogen cyanide

Reference

  1. ೧.೦ ೧.೧ ೧.೨ ೧.೩ Global Substance Registration System, ೧೮ ನವೆಂಬರ್ 2016, ಆಂಗ್ಲ, hydrogen cyanide, 2WTB3V159F
  2. CAS Common Chemistry, ೯ ಏಪ್ರಿಲ್ 2021, https://commonchemistry.cas.org/detail?cas_rn=74-90-8, LELOWRISYMNNSU-UHFFFAOYSA-N
  3. ೩.೦ ೩.೧ ChEMBL, ೧೮ ನವೆಂಬರ್ 2016, ಆಂಗ್ಲ, CYANIDE, CHEMBL183419
  4. ೪.೦ ೪.೧ inferred from InChIKey
  5. ೫.೦ ೫.೧ ೫.೨ ೫.೩ ೫.೪ LELOWRISYMNNSU-UHFFFAOYSA-N, InChIKey
  6. ECHA Substance Infocard database, ೨೭ ಡಿಸೆಂಬರ್ 2018, 100.000.747, Hydrogen cyanide, CAS no.: 74-90-8
  7. ನ್ಯಾಷನಲ್ ಲೈಬ್ರರಿ ಇಸ್ರೇಲ್
  8. Freebase Data Dumps, ೨೮ ಅಕ್ಟೋಬರ್ 2013
  9. ೯.೦ ೯.೧ ChEBI, ೫ ಅಕ್ಟೋಬರ್ 2016, ಆಂಗ್ಲ, hydrogen cyanide, 18407
  10. ೧೦.೦ ೧೦.೧ ೧೦.೨ ೧೦.೩ ೧೦.೪ ೧೦.೫ PubChem, ೧೮ ನವೆಂಬರ್ 2016, ಆಂಗ್ಲ, 768, hydrogen cyanide
  11. UniChem
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  13. Nuovo soggettario
  14. ChemSpider, ೧೮ ನವೆಂಬರ್ 2016, ಆಂಗ್ಲ, 748, Hydrogen cyanide
  15. OpenAlex, ೨೬ ಜನವರಿ 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
  16. Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard
  17. ChEBI release 2020-09-01
  18. Cannabis Database
  19. InChI=1S/CHN/c1-2/h1H, International Chemical Identifier
  20. Nuovo soggettario, https://thes.bncf.firenze.sbn.it/termine.php?id=32544, ೧೫ ಜೂನ್ 2021
  21. KBpedia, ೯ ಜುಲೈ 2020
  22. ೩ ಏಪ್ರಿಲ್ 2019, https://github.com/JohnMarkOckerbloom/ftl/blob/master/data/wikimap
  23. Hazardous Substances Data Bank, ೧೦ ಮೇ 2021, ೨೮ ಅಕ್ಟೋಬರ್ 2019, Hydrogen cyanide, 165
  24. ೨೪.೦ ೨೪.೧ ೨೪.೨ ೨೪.೩ ೨೪.೪ ೨೪.೫ ೨೪.೬ ೨೪.೭ ೨೪.೮ Gene Ontology release 2020-05-02, Rhea release 113
  25. ೨೫.೦ ೨೫.೧ ೧ ಫೆಬ್ರವರಿ 2021, http://geneontology.org/external2go/rhea2go
  26. ೨೬.೦ ೨೬.೧ ೨೬.೨ ೨೬.೩ ೨೬.೪ Gene Ontology release 2022-07-01
  27. ೨೭.೦೦ ೨೭.೦೧ ೨೭.೦೨ ೨೭.೦೩ ೨೭.೦೪ ೨೭.೦೫ ೨೭.೦೬ ೨೭.೦೭ ೨೭.೦೮ ೨೭.೦೯ ೨೭.೧೦ http://www.cdc.gov/niosh/npg/npgd0333.html
  28. Hard-luck Scheele
  29. ChEBI release 2021-03-01
  30. ೩೦.೦ ೩೦.೧ ೩೦.೨ ೩೦.೩ Basic laboratory and industrial chemicals: A CRC quick reference handbook
  31. https://www.aqua-calc.com/page/density-table/substance/hydrogen-blank-cyanide-coma-and-blank-gas
  32. https://cameochemicals.noaa.gov/chemical/3599
  33. Modification of Tobacco Smoke
  34. Analysis of the volatile constituents of black chokeberry (Aronia melanocarpa Ell.)
  35. Cyanide poisoning of goats from sugar gums (Eucalyptus cladocalyx).
  36. ೩೬.೦ ೩೬.೧ Cyanide content of cassava (Manihot esculenta, Euphorbiaceae) cultivars used by Tukanoan Indians in Northwest Amazonia
  37. Cyanide exposure from linseed
  38. ೩೮.೦ ೩೮.೧ ೩೮.೨ ೩೮.೩ ೩೮.೪ Polyphenols, Phytate, Cyanogenic Glycosides, and Trypsin Inhibitor Activity of Several Philippine Indigenous Food Legumes
  39. A method for the practical quantification and kinetic evaluation of cyanogenesis in plant material. Application toPteridium aquilinum andPassiflora capsularis
  40. ೪೦.೦ ೪೦.೧ Spectrophotometer-aided evaluation of cyanogenic potential in white clover (Trifolium repens L.)
  41. ೪೧.೦ ೪೧.೧ ೪೧.೨ ೪೧.೩ The Cyanide Content of Laetrile Preparations, Apricot, Peach and Apple Seeds
  42. A community-driven global reconstruction of human metabolism.
  43. A comprehensive genome-scale reconstruction of Escherichia coli metabolism--2011.
  44. Biogenetically diverse, bioactive constituents of a sponge, order Verongida: bromotyramines and sesquiterpene-shikimate derived metabolites
  45. ATP-dependent reduction of azide and HCN by N2-fixing enzymes of Azotobacter vinelandii and Clostridium pasteurianum.
  46. BitterDB
  47. Medical Subject Headings, ೧೫ ಮಾರ್ಚ್ 2018, D006856
  48. Nuremberg Trials Project, https://nuremberg.law.harvard.edu/documents/5031-affidavit-concerning-the-concentration?q=Georg+Konrad+Morgen#p.10
  49. Reactome, https://reactome.org/PathwayBrowser/#/R-HSA-1430728&DTAB=MT
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