Acetonitrile (CAS 75-05-8)

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Acetonitrile. CAS 75-05-8.

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Data transcribed from regulatory registers and technical literature, with the source and edition stated. It does not replace the supplier's safety data sheet. Fields without a recorded source are marked as such.

Chemical Overview: Acetonitryl
Molecular formulaC2H3N
Molecular weight41.05 g/mol
Melting point-43.85 °C
Boiling point81.65 °C (760 mmHg)
Density0.7857 g/cm³
LogP (lipophilicity)-0.34
pKa25
SMILESCC#N

Synonyms: Acetonitrile · Methyl cyanide

Data sources: PubChem (NLM/NIH), Reid, Prausnitz, Poling 4th ed. (1987)
Last updated: 2026-09-02

SCIENTIFIC RESEARCH

[1]Core2025
05 CE-20250002933198-signed
05 CE-20250002933198-signed, 05 CE-20250002933198-signed. (2025). "05 CE-20250002933198-signed". 05 CE-20250002933198-signed.
[2]PubMed2025
Blumberg LM, Desmet G. (2025). "Generic gradient elution RPLC analyses.". Journal of chromatography. A. https://doi.org/10.1016/j.chroma.2025.465999
[3]PubMed2025
Liu T, Chen H, Song Y et al.. (2025). "Plasma Fractionation and Mixture Improves Coverage in Proteomic Analysis.". Journal of proteome research. https://doi.org/10.1021/acs.jproteome.5c00814
[4]PubMed2024
Kalinke N, Stopper P, Völkl L et al.. (2024). "SWIEET-a salt-free alternative to QuEChERS.". Analytical and bioanalytical chemistry. https://doi.org/10.1007/s00216-024-05525-0
[5]PubMed2024
Hegedüs Z, Gömöri C, Varga M et al.. (2024). "Separation of ochratoxins by centrifugal partition chromatography.". Journal of chromatography. A. https://doi.org/10.1016/j.chroma.2024.464898
[6]PubMed2024
Derwand D, Rzeppa S, Voss SC et al.. (2024). "QuEChERS as alternative extraction procedure in doping analyses.". Drug testing and analysis. https://doi.org/10.1002/dta.3610
[7]PubMed2024
Modrušan M, Glazer L, Otmačić L et al.. (2024). "Anion-Binding Properties of Short Linear Homopeptides.". International journal of molecular sciences. https://doi.org/10.3390/ijms25105235
[8]PubMed2021
Martin-Diaz J, Molina-Espeja P, Hofrichter M et al.. (2021). "Directed evolution of unspecific peroxygenase in organic solvents.". Biotechnology and bioengineering. https://doi.org/10.1002/bit.27810
📚 Scientific references (Chicago Author-Date) 19 refs · 3 baz

MOLECULE Per-CAS bibliography (live from 13+ databases)

Sources: db:core (1) · db:pubmed (15) · db:crossref (3)

  1. db:core 05 CE-20250002933198-signed, 05 CE-20250002933198-signed. (2025). "05 CE-20250002933198-signed". 05 CE-20250002933198-signed.
  2. db:pubmed Blumberg LM, Desmet G. (2025). "Generic gradient elution RPLC analyses.". Journal of chromatography. A. https://doi.org/10.1016/j.chroma.2025.465999
  3. db:pubmed Liu T, Chen H, Song Y et al.. (2025). "Plasma Fractionation and Mixture Improves Coverage in Proteomic Analysis.". Journal of proteome research. https://doi.org/10.1021/acs.jproteome.5c00814
  4. db:pubmed Kalinke N, Stopper P, Völkl L et al.. (2024). "SWIEET-a salt-free alternative to QuEChERS.". Analytical and bioanalytical chemistry. https://doi.org/10.1007/s00216-024-05525-0
  5. db:pubmed Hegedüs Z, Gömöri C, Varga M et al.. (2024). "Separation of ochratoxins by centrifugal partition chromatography.". Journal of chromatography. A. https://doi.org/10.1016/j.chroma.2024.464898
  6. db:pubmed Derwand D, Rzeppa S, Voss SC et al.. (2024). "QuEChERS as alternative extraction procedure in doping analyses.". Drug testing and analysis. https://doi.org/10.1002/dta.3610
  7. db:pubmed Modrušan M, Glazer L, Otmačić L et al.. (2024). "Anion-Binding Properties of Short Linear Homopeptides.". International journal of molecular sciences. https://doi.org/10.3390/ijms25105235
  8. db:pubmed Martin-Diaz J, Molina-Espeja P, Hofrichter M et al.. (2021). "Directed evolution of unspecific peroxygenase in organic solvents.". Biotechnology and bioengineering. https://doi.org/10.1002/bit.27810
  9. db:pubmed Dank C, Wurzer R, Felsinger S et al.. (2020). "A Many-Faced Alkaloid: Polymorphism of (-)-Monophyllidin.". Molecules (Basel, Switzerland). https://doi.org/10.3390/molecules25030449
  10. db:pubmed Klatt MG, Mack KN, Bai Y et al.. (2020). "Solving an MHC allele-specific bias in the reported immunopeptidome.". JCI insight. https://doi.org/10.1172/jci.insight.141264
  11. db:pubmed Liu Y, Ma X, Zhou M et al.. (2020). "An effective method to produce 7-epitaxol from taxol in HCO(3)().". Bioorganic & medicinal chemistry letters. https://doi.org/10.1016/j.bmcl.2020.127285
  12. db:pubmed Nuckowski Ł, Kilanowska A, Studzińska S. (2020). "Hydrophilic interaction in solid-phase extraction of antisense oligonucleotides.". Journal of chromatographic science. https://doi.org/10.1093/chromsci/bmz114
  13. db:pubmed Kogawa AC, Pires AEDT, Salgado HRN. (2019). "Atorvastatin: A Review of Analytical Methods for Pharmaceutical Quality Control and Monitoring.". Journal of AOAC International. https://doi.org/10.5740/jaoacint.18-0200
  14. db:pubmed Li J, Ha NS, Liu T' et al.. (2019). "Ionic-surfactant-mediated electro-dewetting for digital microfluidics.". Nature. https://doi.org/10.1038/s41586-019-1491-x
  15. db:pubmed Humbert MT, Zhang Y, Maginn EJ. (2019). "PyLAT: Python LAMMPS Analysis Tools.". Journal of chemical information and modeling. https://doi.org/10.1021/acs.jcim.9b00066
  16. db:pubmed Berger N, Wollny LJB, Sokkar P et al.. (2019). "Solvent-Enhanced Conformational Flexibility of Cyclic Tetrapeptides.". Chemphyschem : a European journal of chemical physics and physical chemistry. https://doi.org/10.1002/cphc.201900345
  17. db:crossref Svasti Haricharan, Powel H Brown. (2015). "Abstract P4-05-05: A novel TP53-dependent role for TLR4 in driving breast cancer". Cancer Research. https://doi.org/10.1158/1538-7445.sabcs14-p4-05-05
  18. db:crossref (2005). "Breaker page". 2005 IEEE Workshop on Microelectronics and Electron Devices, 2005. WMED '05.. https://doi.org/10.1109/wmed.2005.1431623
  19. db:crossref J. Konieczny, C. Shimizu, G. Meyer et al.. (0). "A Handheld Flexible Display System". IEEE Visualization 2005 - (VIS'05). https://doi.org/10.1109/vis.2005.5
Regulatory status of the substance
This substance is subject to regulatory requirements: hazardous waste management (BDO register). Details in the \"Regulatory Status (REACH/ECHA/CLP)\" section and on the SDS. Regulatory information — does not restrict purchase in this store.
🧪 Chemical Data
CAS Number
75-05-8
Molecular formula
C2H3N
Molar mass
41.05 g/mol
SMILES
CC#N
⚗️ Physicochemical properties
Density
0.7857 g/cm³ @ 20°C

Source: PubChem, NIST WebBook. Last updated: 2026-09-02

🔍 External identifiers
9 of 16 ID systems56%
DatabaseIdentifierActions
CAS Registry Number75-05-8Open →
PubChem CID6342[1]Open →
SMILESCC#N[1]
EC Number200-835-2[2]Open →
HMDBHMDB0061869Open →
ChemSpider6102[3]Open →
UNII (FDA)Z072SB282NOpen →
NSC Number (NCI)7593Open →
WikiData QIDQ408047Open →

Sources: PubChem (NIH), Wikidata SPARQL, KEGG, ChEMBL (EBI), CompTox CTX (EPA).

📚 Scientific references (Chicago Author-Date) (3 sources)
  1. PubChem. National Center for Biotechnology Information (NIH/NLM), chemical compound database. dotyczy: PubChem CID · SMILES
  2. ECHA. EC Inventory — EINECS, ELINCS, NLP and List Numbers assigned under REACH. Helsinki: European Chemicals Agency. dotyczy: EC Number
  3. ChemSpider. Royal Society of Chemistry, chemical structure database. dotyczy: ChemSpider

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Acetonitrile — CAS 75-05-8. Listed by Shandong Yuanlian. Prepared from the supplier’s public catalogue; not verified against their internal data.

Data from PubChemSource: PubChem (NIH)