- 関
 
- thiocyanate
 
WordNet
- a salt of thiocyanic acid; formed when alkaline cyanides are fused with sulfur
 
- street name for lysergic acid diethylamide (同)back breaker, battery-acid, dose, dot, Elvis, loony toons, Lucy in the sky with diamonds, pane, superman, window pane, Zen
 
- any of various water-soluble compounds having a sour taste and capable of turning litmus red and reacting with a base to form a salt
 
- having the characteristics of an acid; "an acid reaction"
 
PrepTutorEJDIC
- 酸性の / 酸味のある,すっぱい(sour) / (言葉・態度などが)厳しい,しんらつな / 酸 / すっぱいもの / 《俗》=LSD
 
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2015/08/27 16:02:22」(JST)
[Wiki en表示]
Thiocyanic acid[1]
| 
 | 
 | 
| Names | 
| IUPAC name
 Nitridosulfanidocarbon[2] 
 | 
Other names
- Hydrogen thiocyanate[citation needed]
 
- Sulfocyanic acid[citation needed]
 
- Sulfocyanide[citation needed]
 
 
 
 
 | 
| Identifiers | 
| 
 CAS Registry Number 
 | 
463-56-9 Y | 
| 3DMet | 
B00344 | 
| ChEBI | 
CHEBI:29200 Y | 
| ChEMBL | 
ChEMBL84336 Y | 
| ChemSpider | 
760 Y | 
| EC number | 
207-337-4 | 
| 
 Gmelin Reference 
 | 
25178 | 
InChI 
- 
InChI=1S/CHNS/c2-1-3/h3H Y 
Key: ZMZDMBWJUHKJPS-UHFFFAOYSA-N Y 
 
 
 
 | 
| Jmol-3D images | 
Image | 
| KEGG | 
C01755 N | 
| MeSH | 
thiocyanic+acid | 
| PubChem | 
781 | 
| 
 | 
| Properties | 
| 
 Chemical formula 
 | 
CHNS | 
| Molar mass | 
59.09 g·mol−1 | 
| Appearance | 
colorless, oily liquid | 
| Odor | 
pungent | 
| Density | 
2.04 g/cm3 | 
| Melting point | 
5 °C (41 °F; 278 K) | 
| 
 Solubility in water 
 | 
Miscible | 
| Solubility | 
soluble in ethanol, diethyl ether | 
| log P | 
0.429 | 
| Acidity (pKa) | 
0.926 | 
| Basicity (pKb) | 
13.071 | 
| Hazards | 
| EU classification | 
 Xn | 
| R-phrases | 
R20/21/22, R32, R52/53 | 
| S-phrases | 
(S2), S13 | 
| Related compounds | 
| 
 Related  alkanenitriles 
 | 
- Hydrogen cyanide
 
- Cyanogen iodide
 
- Cyanogen bromide
 
- Cyanogen chloride
 
- Cyanogen fluoride
 
- Acetonitrile
 
- Aminoacetonitrile
 
- Glycolonitrile
 
- Cyanogen
 
 
 
 | 
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). 
 
 | 
|  N verify (what is: Y/N?) | 
| Infobox references | 
 | 
 | 
Thiocyanic acid is a chemical compound with the formula HSCN that exists as a mixture with the isomeric compound isothiocyanic acid (HNCS).[3] It is the sulfur analog of cyanic acid (HOCN).
It is a weak acid, bordering on strong, with a pKa of 1.1 at 20 °C and extrapolated to zero ionic strength.[4]
HSCN is predicted to have a triple bond between carbon and nitrogen. It has been observed spectroscopically but has not been isolated as a pure substance.[5]
The salts and esters of thiocyanic acid are known as thiocyanates. The salts are composed of the thiocyanate ion (−SCN) and a suitable metal cation (e.g., potassium thiocyanate, KSCN). The esters of thiocyanic acid have the general structure R-SCN.
References
- ^ Merck Index, 11th Edition, 9257.
 
- ^ "thiocyanic acid (CHEBI:29200)". Chemical Entities of Biological Interest. USA: European Bioinformatics Institute. 18 October 2009. Main. Retrieved 5 June 2012. 
 
- ^ Holleman, A. F.; Wiberg, E. Inorganic Chemistry Academic Press: San Diego, 2001. ISBN 0-12-352651-5.
 
- ^ Martell, A. E.; Smith, R. M.; Motelaitis, R. J. NIST Database 46 National Institute of Standards and Technology: Gaithersburg, MD, 2001.
 
- ^ Wierzejewska, M.; Mielke, Z. (2001). "Photolysis of Isothiocyanic Acid HNCS in Low-Temperature Matrices. Infrared Detection of HSCN and HSNC Isomers". Chemical Physics Letters 349: 227–234. doi:10.1016/S0009-2614(01)01180-0. 
 
 
| 
 Molecules detected in outer space 
 | 
 
 | 
 
| Molecules | 
 | 
 
 | 
 
Deuterated 
molecules | 
- Ammonia
 
- Ammonium ion
 
- Formaldehyde
 
- Formyl radical
 
- Heavy water
 
- Hydrogen cyanide
 
- Hydrogen deuteride
 
- Hydrogen isocyanide
 
- Methylacetylene
 
- N2D+
 
- Trihydrogen cation
 
 
 
 | 
 
 | 
 
| Unconfirmed | 
- Anthracene
 
- Dihydroxyacetone
 
- Ethyl methyl ether
 
- Glycine
 
- Graphene
 
- H2NCO+
 
- Linear C5
 
- Naphthalene cation
 
- Phosphine
 
- Pyrene
 
- Silylidine
 
 
 
 | 
 
 | 
 
| Related | 
- Abiogenesis
 
- Astrobiology
 
- Astrochemistry
 
- Atomic and molecular astrophysics
 
- Chemical formula
 
- Circumstellar envelope
 
- Cosmic dust
 
- Cosmic ray
 
- Cosmochemistry
 
- Diffuse interstellar band
 
- Extraterrestrial life
 
- Extraterrestrial liquid water
 
- Forbidden mechanism
 
- Helium hydride ion
 
- Homochirality
 
- Intergalactic dust
 
- Interplanetary medium
 
- Interstellar medium
 
- Iron–sulfur world theory
 
- Kerogen
 
- Life
 
- Molecules in stars
 
- Nexus for Exoplanet System Science
 
- Organic compound
 
- Outer space
 
- PAH world hypothesis
 
- Panspermia
 
- Polycyclic aromatic hydrocarbon (PAH)
 
- RNA world hypothesis
 
- Spectroscopy
 
- Tholin
 
 
 
 | 
 
 | 
 
-  Book:Chemistry
 
-  Category:Astrochemistry
 
-  Category:Molecules
 
-  Portal:Astrobiology
 
-  Portal:Chemistry
 
 
 
 | 
 
 
 | 
 
UpToDate Contents
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English Journal
- Avidity of IgG antibodies against meningococcal serogroup a polysaccharide and correlations with bactericidal activity in sera from meningitis patients and controls from Ethiopia.
 
- Medhane M1, Tunheim G, Naess LM, Mihret W, Bedru A, Norheim G, Petros B, Aseffa A, Rosenqvist E.
 
- Scandinavian journal of immunology.Scand J Immunol.2014 Apr;79(4):267-75. doi: 10.1111/sji.12150.
 
- Meningococcal meningitis is a significant global health challenge, especially for sub-Saharan area: the African meningitis belt. Neisseria meningitidis of serogroup A (MenA) is responsible for the large number of epidemics that have been recorded in these countries. To determine the level of antibod
 
- PMID 24383864
 
- Ion association in aqueous solutions probed through vibrational energy transfers among cation, anion, and water molecules.
 
- Li J1, Bian H, Chen H, Wen X, Hoang BT, Zheng J.
 
- The journal of physical chemistry. B.J Phys Chem B.2013 Apr 25;117(16):4274-83. doi: 10.1021/jp3053373. Epub  2012 Sep 14.
 
- KSCN and NH4SCN aqueous solutions were investigated with intermolecular vibrational energy transfer methods. In a KSCN/H2O (1/10 molar ratio) solution, 90% of the initial excitation of the CN stretch (~2066 cm(-1)) of the SCN(-) anion is transferred to the HOH bending mode (~1636 cm(-1)) of water mo
 
- PMID 22928938
 
- Development of ultrasound-assisted emulsification microextraction for determination of thiocynate ion in human urine and saliva samples.
 
- Hashemi M1, Daryanavard SM, Abdolhosseini S.
 
- Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.J Chromatogr B Analyt Technol Biomed Life Sci.2013 Feb 15;917-918:5-10. doi: 10.1016/j.jchromb.2012.12.030. Epub  2013 Jan 8.
 
- Ultrasound-assisted emulsification microextraction (USAE-ME) procedure coupled with UV-vis spectrophotometric measurement has been developed for determination of thiocyanate ion (SCN(-)) in water and biological fluids samples. The method is based on protonation of SCN(-) ions in acidic medium and ex
 
- PMID 23353810
 
Japanese Journal
- Nitrite Reductase 遺伝子を標的としたPCR-DGGE法によるコークス炉廃水処理活性汚泥中の脱窒細菌群集構造の解析
 
- 水環境学会誌 = Journal of Japan Society on Water Environment 27(4), 249-254, 2004-04-10
 
- NAID 10012886542
 
- 強塩基性陰イオン交換樹脂 : チオシアン酸系からの金属イオンの分離
 
- 薄膜の形成と構造  硫酸パラジウム(II)溶液からのパラジウム電析におけるピロリン酸二水素カリウムおよびホウ酸の効果
 
★リンクテーブル★
  [★]
- 英
 
- thiocyanic acid、thiocyanate
 
- 関
 
- チオシアナート、チオシアネート、チオシアン酸塩