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tetracyanoethylene

CAS No. 670-54-2 | PubChem CID 12635
Section 1. Identification
Chemical Nametetracyanoethylene CAS No.670-54-2
Synonymsethene tetracarboni-trile Chinese Name四氰基乙烯
Molecular FormulaC6N Molecular Weight128.091
UN No.2811 Data SourcePubChem (NIH/NLM)
GHS Hazard Classification
Signal Word DANGER
Pictograms GHS06 · Acute Toxic GHS07 · Irritant
Hazard Statements H300H310H312H315H319H332H335
Precautionary Statements P261P262P264P264+P265P270P271P280P301+P316P302+P352P304+P340P305+P351+P338P316P317P319P321P330P332+P317P337+P317P361+P364P362+P364P403+P233P405P501

Section 2. Hazards Identification

H300 (100%): Fatal if swallowed [Danger Acute toxicity, oral]

H310 (10.9%): Fatal in contact with skin [Danger Acute toxicity, dermal]

H312 (84.8%): Harmful in contact with skin [Warning Acute toxicity, dermal]

H315 (15.2%): Causes skin irritation [Warning Skin corrosion/irritation]

H319 (15.2%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]

H332 (84.8%): Harmful if inhaled [Warning Acute toxicity, inhalation]

H335 (13%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

P261, P262, P264, P264+P265, P270, P271, P280, P301+P316, P302+P352, P304+P340, P305+P351+P338, P316, P317, P319, P321, P330, P332+P317, P337+P317, P361+P364, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 46 reports by companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.

Section 9. Physical and Chemical Properties

Solid; [Merck Index] Colorless crystalline solid; [Alfa Aesar MSDS]

Schoenflies notation

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Nitrogen Compounds -> Nitriles

Section 11. Toxicological Information

Organic nitriles decompose into cyanide ions both in vivo and in vitro. Consequently the primary mechanism of toxicity for organic nitriles is their production of toxic cyanide ions or hydrogen cyanide. Cyanide is an inhibitor of cytochrome c oxidase in the fourth complex of the electron transport chain (found in the membrane of the mitochondria of eukaryotic cells). It complexes with the ferric iron atom in this enzyme. The binding of cyanide to this cytochrome prevents transport of electrons from cytochrome c oxidase to oxygen. As a result, the electron transport chain is disrupted and the cell can no longer aerobically produce ATP for energy. Tissues that mainly depend on aerobic respiration, such as the central nervous system and the heart, are particularly affected. Cyanide is also known produce some of its toxic effects by binding to catalase, glutathione peroxidase, methemoglobin, hydroxocobalamin, phosphatase, tyrosinase, ascorbic acid oxidase, xanthine oxidase, succinic dehydrogenase, and Cu/Zn superoxide dismutase. Cyanide binds to the ferric ion of methemoglobin to form inactive cyanmethemoglobin. (L97)

No indication of carcinogenicity to humans (not listed by IARC).

Exposure to high levels of cyanide for a short time harms the brain and heart and can even cause coma, seizures, apnea, cardiac arrest and death. Chronic inhalation of cyanide causes breathing difficulties, chest pain, vomiting, blood changes, headaches, and enlargement of the thyroid gland. Skin contact with cyanide salts can irritate and produce sores. (L96, L97)

Oral (L96) ; inhalation (L96) ; dermal (L96)

Cyanide poisoning is identified by rapid, deep breathing and shortness of breath, general weakness, giddiness, headaches, vertigo, confusion, convulsions/seizures and eventually loss of consciousness. (L96, L97)

Other Poison - Chemical Asphyxiant

Antidotes to cyanide poisoning include hydroxocobalamin and sodium nitrite, which release the cyanide from the cytochrome system, and rhodanase, which is an enzyme occurring naturally in mammals that combines serum cyanide with thiosulfate, producing comparatively harmless thiocyanate. Oxygen therapy can also be administered. (L97)

Source: PubChem CID 12635 (NIH/NLM, public domain). Retrieved from PubChem, a public-domain chemistry database maintained by the U.S. National Library of Medicine. Last updated: 2026-08-02 09:57:47.
Disclaimer: This information is compiled for reference only and does not replace the manufacturer's official Safety Data Sheet. Always consult the supplier's SDS before handling any chemical.