1,2,4-Triazol

1H-1,2,4-Triazole

HCID 9257CAS 288-88-0

Grundinformationen

Standard-SMILES
c1nc[nH]n1
InChIKey
NSPMIYGKQJPBQR-UHFFFAOYSA-N
Summenformel
C2H3N3
Durchschnittliche Molmasse
69,07 g/mol
Monoisotopische Masse
69,03269711

Namen und Bezeichner

Bevorzugter Name
1H-1,2,4-Triazole
IUPAC
1H-1,2,4-triazole
Lokaler Name
1,2,4-Triazol
Englischer Name
1,2,4-Triazole
Summenformel
C2H3N3
Molmasse
69.07

Namen und Synonyme

1,2,4-TRIAZOLE1H-1,2,4-Triazole288-88-0Pyrrodiazoles-TriazoleDTXSID602713110MS0Y1RDINSC-83128DTXCID207131CHEBI:35550RefChem:908322CHEBI:35560
Weitere Namen anzeigen
TRIAZOLETA-4TRIAZOLE(1,2,4-)
206-022-94H-1,2,4-triazole63598-71-01,2,4-1H-TriazoleMFCD000052281H-1,2,4-triazol1,2,4 triazole1,2,4-triazol

Datenbank-Bezeichner

CAS
288-88-0、63598-71-0
PubChem CID
9257
DTXSID
DTXSID6027131
ChEMBL
CHEMBL15571
ChEBI
CHEBI:35550
UNII
10MS0Y1RDI
EC Number
206-022-9
Nikkaji
J5.455K

Eigenschaften

Berechnete Struktureigenschaften

XLogP
-0,6
Polarare Oberfläche (TPSA)
41,6 Ų
H-Brücken-Donoren
1
H-Brücken-Akzeptoren
2
Frei drehbare Bindungen
0
Schwere Atome
5

Experimentelle und physikochemische Eigenschaften

LogP · 2 Einträge

log Kow = -0.58

-0.6

Density640 kg/m³
Color/FormNeedles from benzene/ethanol
Solubility · 2 Einträge

Soluble in water, ethanol

Solubility in water, g/100ml at 20 °C: 125

Flash Point · 2 Einträge

170 °C closed cup

170 °C c.c.

Boiling Point · 2 Einträge

260 °C (decomposes)

260 °C

Physikochemische Eigenschaften

Schmelzpunkt
119 · 119-121 °C (lit.)
Siedepunkt
260 °C · 260 °C (lit.)
Dichte
1.15 g/cm3 · 1.15 g/cm3 (130℃)
Dampfdruck
0.215 Pa · 0.215Pa at 20℃
Brechungsindex
1.4854 · 1.4854 (estimate)
Flammpunkt
140 °C · 140 °C

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 6 Einträge

Danger

H302: Harmful if swallowed [Warning Acute toxicity, oral];H319: Causes serious eye irritation [Warning Serious eye damage/eye irritation];H360FD: May damage fertility; May damage the unborn child [Danger Reproductive toxicity]

P203, P264, P264+P265, P270, P280, P301+P317, P305+P351+P338, P318, P330, P337+P317, P405, and P501 (click each P-code to see the statement)

Danger

Gefahrenhinweise

Regulatory Information · 6 Einträge

Chemical: 1H-1,2,4-Triazole

Hazard Traits - Reproductive Toxicity;Authoritative List - EC Annex VI CMRs - Cat. 1B;Report - if used as a fragrance or flavor ingredient

Regulation (EC) No 1107/2009 (amended)

1H-1,2,4-Triazole is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of 1H-1,2,4-Triazole are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

1,2,4-Triazole is listed in the dataset of EPA Human Health Benchmarks for Pesticides under the Safe Drinking Water Act (40 eCFR 141)

Status: Active Update: 26-04-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/13353

Other Safety InformationIMAP assessments - 1H-1,2,4-Triazole: Human health tier II assessment
Fire HazardsCombustible. Gives off irritating or toxic fumes (or gases) in a fire. Finely dispersed particles form explosive mixtures in air.
Fire PotentialCombustible
Hazards SummaryAn eye irritant; Can be absorbed through skin; Animal tests show that this substance possibly causes toxicity to human reproduction or development. [ICSC] An eye irritant; [eChemPortal: ERMA; ESIS] An irritant; [MSDSonline]
EC ClassificationSymbol: Xn; R: 22-36-63; S: (2)-36/37

Sicherheit und Schutzausrüstung

Fire FightingUse water spray, powder, foam, carbon dioxide.
First Aid Measures · 4 Einträge

Fresh air, rest.

Remove contaminated clothes. Remove contaminated clothes. Rinse skin with plenty of water or shower.

First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.

Rinse mouth. Give one or two glasses of water to drink. Refer for medical attention .

Safe StorageSeparated from strong oxidants and strong acids. Store in an area without drain or sewer access.
Fire Fighting Procedures · 2 Einträge

Suitable extinguishing media: Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide. Special protective equipment for fire-fighters: Wear self contained breathing apparatus for fire fighting if necessary.

Powder, water spray, foam, carbon dioxide.

Storage Conditions · 2 Einträge

Keep container tightly closed in a dry and well-ventilated place.

Separated from strong oxidants, and strong acids. Store in an area without drain or sewer access.

Cleanup Methods · 2 Einträge

Accidental Release Measures. Personal precautions: Use personal protective equipment. Avoid dust formation. Avoid breathing dust. Ensure adequate ventilation. Environmental precautions: Do not let product enter drains. Methods for cleaning up: Pick up and arrange disposal without creating dust. Keep in suitable, closed containers for disposal.

Do NOT let this chemical enter the environment. Sweep spilled substance into sealable containers; if appropriate, moisten first to prevent dusting. Carefully collect remainder, then remove to safe place.

Toxikologische Informationen

Environmental Fate · 3 Einträge

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 5(SRC), determined from a structure estimation method(2), indicates that 1H-1,2,4-triazole is expected to have very high mobility in soil(SRC). Volatilization of 1H-1,2,4-triazole from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 1.5X10-6 atm-cu m/mole(SRC), using a fragment constant estimation method(3). 1H-1,2,4-Triazole is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 0.6 mm Hg at 25 °C(SRC), determined from a fragment constant method(4). Biodegradation data in soil were not available(SRC, 2010).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 5(SRC), determined from a structure estimation method(2), indicates that 1H-1,2,4-triazole is not expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is expected(3) based upon an estimated Henry's Law constant of 1.5X10-6 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 20 and 150 days, respectively(SRC). According to a classification scheme(5), an estimated BCF of 3(SRC), from its log Kow of -0.58(6) and a regression-derived equation(7), suggests the potential for bioconcentration in aquatic organisms is low(SRC). 1H-1,2,4-Triazole is not expected to undergo hydrolysis in the environment due to the lack of functional groups that hydrolyze under environmental conditions(3). Biodegradation data in water were not available(SRC, 2010).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), 1H-1,2,4-triazole, which has an estimated vapor pressure of 0.6 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase 1H-1,2,4-triazole is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 160 days(SRC), calculated from its rate constant of 1.0X10-13 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). 1H-1,2,4-Triazole contains chromophores that absorb at wavelengths >290 nm(4) and therefore may be susceptible to direct photolysis by sunlight(SRC).

Adverse Effects · 1 Eintrag

Reproductive Toxin - A chemical that is toxic to the reproductive system, including defects in the progeny and injury to male or female reproductive function. Reproductive toxicity includes developmental effects. See Guidelines for Reproductive Toxicity Risk Assessment.

Exposure RoutesThe substance can be absorbed into the body in hazardous amounts by ingestion. The substance can be absorbed into the body by inhalation and through the skin.
Signs and SymptomsRedness. Pain.
ICSC Environmental DataThe substance is harmful to aquatic organisms. This substance does enter the environment under normal use. Great care, however, should be taken to avoid any additional release, for example through inappropriate disposal.
Soil Adsorption/Mobility · 1 Eintrag

Using a structure estimation method based on molecular connectivity indices(1), the Koc of 1H-1,2,4-triazole can be estimated to be 5(SRC). According to a classification scheme(2), this estimated Koc value suggests that 1H-1,2,4-triazole is expected to have very high mobility in soil.

Regulatorische Informationen

Regulatory Information · 6 Einträge

Chemical: 1H-1,2,4-Triazole

Hazard Traits - Reproductive Toxicity;Authoritative List - EC Annex VI CMRs - Cat. 1B;Report - if used as a fragrance or flavor ingredient

Regulation (EC) No 1107/2009 (amended)

1H-1,2,4-Triazole is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of 1H-1,2,4-Triazole are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

1,2,4-Triazole is listed in the dataset of EPA Human Health Benchmarks for Pesticides under the Safe Drinking Water Act (40 eCFR 141)

Status: Active Update: 26-04-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/13353

Sicherheitsdaten

wgk
2
tsca
TSCA listed
hs_code
29339990
RTECS-Nr.
XZ3806000
risk_code
22-36-63-34
Toxizität
LD50 orally in Rabbit: 1650 mg/kg LD50 dermal Rabbit 3129 - 4200 mg/kg

Chemie und Industrie

Pharmakologische Informationen

Absorption, Distribution and Excretion · 5 Einträge

After a single oral administration of 1 mg/kg bw (test substance (14)C-labeled) to male rats (strain not given), approx 100% of the (14)C activity was absorbed from the digestive tract.

8 hr after a single iv administration of 1 mg/kg bw (test substance (14)C-labeled) to male rats (strain not given), approx 50% of the applied radioactivity was detectable in the body of the animals (gastrointestinal tract not considered). 3 days after the application approx 1.5% of the applied activity could be found, and after 6 days the (14)C-activity was no longer measurable (detection limit 0.3%).

Following a single oral or iv administration of 1 mg/kg bw (test substance (14)C-labeled) to male rats (strain not given), approx. 0.1% of the (14)C-activity was exhaled within 30 hr.

1H-1,2,4-Triazole (14)C-labeled was administered to male rats orally (dose: 1 mg/kg bw) or iv (doses: 0.1, 1, 10, 100 mg/kg bw). Within 48 hr after the single application 92-94% of the (14)C-activity was excreted with the urine and 3-5% with the feces, regardless whether the substance was applied orally or iv.

For more Absorption, Distribution and Excretion (Complete) data for 1H-1,2,4-Triazole (6 total), please visit the HSDB record page.

Verwendung und Herstellung

Uses · 2 Einträge

Used in organic synthesis; [IUCLID]

Intermediate

U.S. Production · 4 Einträge

2023: 5,500,000 - <7,000,000 lb;2022: 7,000,000 - <8,500,000 lb;2021: 4,000,000 - <5,500,000 lb;2020: 4,000,000 - <5,500,000 lb

1H-1,2,4-Triazole is listed as a High Production Volume (HPV) chemical (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and/or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B; 51FR21438).

Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#7598]

Production volume for non-confidential chemicals reported under the 2006 Inventory Update Rule. Chemical: 1H-1,2,4-Triazole. Aggregated National Production Volume: 1 to < 10 million lbs.

Consumer UsesIntermediate
Industry UsesIntermediate
Methods of Manufacturing1,2,4-Triazole is made by reaction between hydrazine and formamide. Distillation.
Use ClassificationEnvironmental transformation -> Pesticide transformation products (metabolite, successor)

Anwendungen

Verwenden1,2,4-Triazole is present in a large variety of fungicides as C14-demethylase-inhibitors. In addition they are used in synthetic chemical reactions such as the design and preparation of ghrelin receptor ligand antagonists, like JMV 2959.

Anbieter13 Anbieter

郑州汇聚化工有限公司0371-53399770 18037166334 · [email protected]
毕佳索(上海毕得医药科技股份有限公司)400-6005915 · [email protected]
Aladdin Scientific[email protected]
上海相辉医药科技有限公司13761987713; 13761987713 · [email protected]
台州南峰药物研究所[email protected] 18616377689 · [email protected]
Ergänzende Hinweise · 1 Eintrag

Definition1,2,4-triazole is a chemical substance with molecular formula C2H3N3, molecular weight 69.07 and CAS No. 288-88-0. Colorless acicular crystal, soluble in water and ethanol. 1H-1,2,4-triazole is a 1,2,4-triazole. It is a tautomer of a 3H-1,2,4-triazole and a 4H-1,2,4-triazole. Triazole is an aromatic five membered heterocyclic compound. Its unique structure is conducive to the formation of a variety of non covalent bonds and is easy to promote the binding of proteins, enzymes and receptors, thus showing a wide range of biological pharmacological activities, such as anticancer, antispasmodic, antibacterial, anti HIV. In particular, 1,2,3-triazole has strong thermal stability and acid-base stability, and is not sensitive to redox, hydrolysis and enzymatic degradation. It is often used as a pharmacodynamic group in drug synthesis.

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