Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
시아누릭 산
시아누르산 · 시아누릭산 · 1,3,5-트리아진-2,4,6(1H,3H,5H)-트리온 · 프세우도시아누르산 · 아이소시아누르산 · 1,3,5-트리아진-2,4,6-트리올 · 2,4,6-SYM-트리아진트리올 · 2,4,6-트리아진트리올
식별자 및 물리적 특성
| CAS No. | 108-80-5 |
|---|---|
| 분자식 | C3H3N3O3 |
| 평균 분자량 | 129.07 g/mol |
| 단동위원소 질량 | 129.01744096 g/mol |
| SMILES | O=c1[nH]c(=O)[nH]c(=O)[nH]1 |
| InChIKey | ZFSLODLOARCGLH-UHFFFAOYSA-N |
| PubChem CID | 7956 |
| ChEMBL | CHEMBL243087 |
| ChEBI | CHEBI:38028 |
| EC No. | 203-618-0 |
| DTXSID | DTXSID7024873 |
| 현지명 | 시아누릭 산 |
화학 및 물리적 성질
| XLogP | -1.2 |
|---|---|
| 극성 표면적 | 87.3 |
| 수소 결합 공여자 수 | 3 |
| 수소 결합 수용자 수 | 3 |
| 회전 가능 결합 수 | 0 |
| 무거운 원자 수 | 9 |
| 형식 전하 | 0 |
| 복잡도 | 135 |
| 물질 분류 | Nitrogen Compounds -> Triazines |
| Polymers | Plastics -> Flame retardantsPlastics -> Polyolefin-IPolyolefin-II |
| pH | pH of saturated aqueous solution @ room temperature = 4.83.8-4.0 (H2O, 20℃)(saturated solution) |
| 냄새 | Odorless회백색 결정, 무취 |
| 맛 | Slightly bitter |
| 밀도 | 2.5 at 68 °F (NTP, 1992) - Denser than waterwill sink1.75 deg 25 °C/4 °C 9 (anhydride)1.66 at 25 °C/4 °C (dihydrate)2.5 g/cm³1.75 @25 °C1.56 |
| Flame Retardants | Flame retardants |
| Color/Form | White crystalline solidCRYSTALLINE POWDER |
| 용해도 | 0.5 mL (NTP, 1992)Slightly soluble in common organic solvents such as acetone, benzene, diethyl ether, ethanol, hexane. Solubility (%): dimethylformamide 7.2diemthyl sulfoxide 17.4.Soluble in hot alcohols, pyridine, concentrated HCL without decompositionin aqueous solutions of NaOH and KOH. Insoluble in cold methanol, ether acetone, benzene chloroform.Solubility in 96% H2SO4 (25 °C): 14.1%Solubility in water (%): 0.2 at 25 °C2.6 at 90 °C10.0 at 150 °CFor more Solubility (Complete) data for CYANURIC ACID (6 total), please visit the HSDB record page.황산, 디메틸포름아미드, 수산화나트륨, 수산화칼륨 및 디메틸술폭시드에 용해됩니다. 아세톤, 벤젠, 디에틸 에테르, 에탄올 및 헥산에 약간 용해됩니다. 차가운 메탄올, 벤젠, 클로로포름에는 용해되지 않습니다. |
| 끓는 점 | DECOMPOSES (NTP, 1992)Sublimes and dissociates to isocyanuric acid at higher />330 °C/ temperatures74 °C |
| Decomposition | The substance decomposes on heating above 320-350 °C producing (highly) toxic fumes including nitrogen oxides and cyanic acid.>320 °C. This produces toxic fumes including nitrogen oxides and isocyanic acid. Reacts with chlorine. This generates explosion hazard. |
| 녹는점 | greater than 680 °F (DEC.) (NTP, 1992)360 °C |
| 증기압 | <0.0001 Pa (25 °C) |
| 굴절률 | 1.4500 (estimate) |
| 저장 조건 | Store below +30°C. |
| 물리적 상태 | 결정성 분말 또는 덩어리 |
| pKa(산도 계수) | 6.88, 11.40, 13.5(at 25℃) |
| 색상 | 흰색~밝은 베이지 |
| 용해도 | 0.3g/100mL(25℃) |
| Merck | 14,2698 |
| BRN | 126982 |
| 헨리 상수 | 1.1×109 mol/(m3Pa) at 25℃, HSDB (2015) |
| 안정성 | 안정적인. 강한 산화제와 호환되지 않습니다. |
| InChI | 1S/C3H3N3O3/c7-1-4-2(8)6-3(9)5-1/h(H3,4,5,6,7,8,9) |
| InChIKey | ZFSLODLOARCGLH-UHFFFAOYSA-N |
| SMILES | O=C1NC(=O)NC(=O)N1 |
| LogP(분배 계수) | -1.31 at 25℃ |
| NIST | 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione(108-80-5) |
| EPA | Cyanuric acid (108-80-5) |
화학적 성질
white powder
안전 및 규제
| GHS 분류 | This chemical does not meet GHS hazard criteria for 73.2% (208 of 284) of all reports.WarningH319 (26.8%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]P264+P265, P280, P305+P351+P338, and P337+P317 (click each P-code to see the statement)Aggregated GHS information provided per 284 reports by companies from 10 notifications to the ECHA C&L Inventory. |
|---|---|
| 규제 정보 | Chemical: 1,3,5-Triazine-2,4,6(1H,3H,5H)-trioneRegulation (EC) No 178/2002 (amended)1,3,5-Triazine-2,4,6(1H,3H,5H)-trione is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione 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)Status: Active Update: 06-08-2018 https://echa.europa.eu/registration-dossier/-/registered-dossier/15028Cyanuric acid: Does not have an individual approval but may be used under an appropriate group standard |
| 기타 안전 정보 | IMAP assessments - 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione: Human health tier I assessment |
| 화재 위험 | Gives off irritating or toxic fumes (or gases) in a fire. |
| 건강 유해성 | SYMPTOMS: Symptoms of exposure to this compound include, local irritation of the eyes. |
| 유해성 요약 | An eye and respiratory tract irritant[HSDB] A mild eye irritantIngestion of large quantity may cause kidney injury[ICSC] An irritant[MSDSonline] Classified as essentially nontoxicAvoid ingestion, inhalation of dust, and contact with eyes[Ullmann] Causes crystals that can damage urinary tract in animals fed high doses[AIHA] |
| 반응성 그룹 | Amides and Imides |
| Special Reports | Hammond BG et alEnviron Health Perspect 69: 287-92 (1986). Chlorinated cyanurates are added to swimming pools as disinfectants. In the presence of water, these materials hydrolyze to yield cyanurate and hypochlorous acid. To evaluate the safety of exposure to these materials, a comprehensive testing program was undertaken. This review summarizes the results of the acute, subchronic, reproduction, metabolism, mutagenesis, and carcinogenicity tests on cyanurate are also summarized. Results from these tests indicate that chlorinated isocyanurates are safe for use in swimming pools. |
| FIFRA 요건 | As the federal pesticide law FIFRA directs, EPA is conducting a comprehensive review of older pesticides to consider their health and environmental effects and make decisions about their future use. Under this pesticide reregistration program, EPA examines health and safety data for pesticide active ingredients initially registered before November 1, 1984, and determines whether they are eligible for reregistration. In addition, all pesticides must meet the new safety standard of the Food Quality Protection Act of 1996. Cyanuric acid is found on List A, which contains most food use pesticides and consists of the 194 chemical cases (or 350 individual active ingredients) for which EPA issued registration standards prior to FIFRA, as amended in 1988. Case No: 0569Pesticide type: antimicrobialRegistration Standard Date: 05/20/88Case Status: RED Approved 09/92OPP has made a decision that some/all uses of the pesticide are eligible for reregistration, as reflected in a Reregistration Eligibility Decision (RED) document.Active ingredient (AI): Cyanuric acidAI Status: The active ingredient is no longer contained in any registered pesticide products ... "cancelled." |
| Reactivity Profile | An amide and amine. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generate mixed oxides of nitrogen (NOx) |
| 대기 기준 | This action promulgates standards of performance for equipment leaks of Volatile Organic Compounds (VOC) in the Synthetic Organic Chemical Manufacturing Industry (SOCMI). The intended effect of these standards is to require all newly constructed, modified, and reconstructed SOCMI process units to use the best demonstrated system of continuous emission reduction for equipment leaks of VOC, considering costs, non air quality health and environmental impact and energy requirements. Cyanuric acid is produced, as an intermediate or a final product, by process units covered under this subpart. |
| Chemical Dangers | Decomposes at >320 °C. This produces toxic fumes including nitrogen oxides and isocyanic acid. Reacts with chlorine. This generates explosion hazard. |
| Air and Water Reactions | Soluble in hot water [Hawley]. |
| 소화 | This compound is not very flammable but any fire involving this compound may produce dangerous vapors. You should evacuate the area. All firefighters should wear full-body protective clothing and use self-contained breathing apparatuses. You should extinguish any fires involving this chemical with a dry chemical, carbon dioxide, foam, or halon extinguisher. (NTP, 1992)Use water spray, alcohol-resistant foam, powder, carbon dioxide. In case of fire: keep drums, etc., cool by spraying with water. |
| 응급 조치 | Fresh air, rest.Rinse and then wash skin with water and soap.Rinse with plenty of water for several minutes (remove contact lenses if easily possible).Rinse mouth. |
| 응급 처치 | EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop. |
| 안전 보관 | Dry. Well closed. Separated from chlorine. |
| 소화 절차 | Water spray, alcohol resistant foam, powder, carbon dioxide. |
| 보관 조건 | Cyanuric acid should be stored in a dry place. Silos and pneumatic conveyors should be grounded to prevent electrostatic discharges....MATERIALS WHICH ARE TOXIC AS STORED OR WHICH CAN DECOMP INTO TOXIC COMPONENTS DUE TO CONTACT WITH...MOISTURE, ACIDS, OR ACID FUMES...STORED IN COOL, WELL-VENTILATED PLACE, OUT OF DIRECT RAYS OF SUN, AWAY FROM...FIRE HAZARD, &...PERIODICALLY INSPECTED & MONITORED. INCOMPATIBLE MATERIALS...ISOLATED... |
| 정리 방법 | Alkali and thermal treatment in filtration and precipitation was used to remove cyanuric acid from wastewaters.Dissolved cyanurate salts are removed from water by treatment with an aq soln of sodium hypochlorite, whereby most of the cyanurate is converted to nitrogen, carbon dioxide, and sodium chloride. The treatment is carried out at pH 9.0-10.0 and 25 deg to 55 °C, the contact time being 2-6 hr. The mol ratio of sodium hypochlorite and cyanurate is kept between 6:1 and 8:1.SODIUM HYPOCHLORITE IS USED IN REMOVAL OF CYANURATES FROM WASTE STREAMS. |
| 비화재 누출 대응 | SMALL SPILLS AND LEAKAGE: If you spill this chemical, you should dampen the solid spill material with water, then transfer the dampened material to a suitable container. Use absorbent paper dampened with water to pick up any remaining material. Seal your contaminated clothing and the absorbent paper in a vapor-tight plastic bag for eventual disposal. Wash all contaminated surfaces with a strong soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned. |
| 처리 방법 | SRP: The most favorable course of action is to use an alternative chemical product with less inherent propensity for occupational exposure or environmental contamination. Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air qualitypotential migration in soil or watereffects on animal, aquatic, and plant lifeand conformance with environmental and public health regulations. |
| 누출 처리 | Personal protection: particulate filter respirator adapted to the airborne concentration of the substance. Sweep spilled substance into covered containers. Carefully collect remainder. Then store and dispose of according to local regulations. |
| Preventive Measures | Impervious protective clothing must be used whenever skin contact is likely. Contaminated work clothing can be cleaned at the facility or sent outside to a contract industrial laundry that has been informed of the potential hazards. Routine washing of hands, face and neck prior to breaks or lunch must be emphasized. Daily showers at the end of the work shift are required. Showers should be immediate for unplanned situations in which overt overexposures can occur such as spills or leaks. |
| Eye Prevention | Wear safety spectacles. |
| 상호 작용 | The major pet food recall associated with acute renal failure in dogs and cats focused initially on melamine as the suspect toxicant. In the course of the investigation, cyanuric acid was identified in addition to melamine in the offending food. The purpose of this study was to characterize the toxicity potential of melamine, cyanuric acid, and a combination of melamine and cyanuric acid in cats. In this pilot study, melamine was added to the diet of 2 cats at 0.5% and 1%, respectively. Cyanuric acid was added to the diet of 1 cat at increasing doses of 0.2%, 0.5%, and 1% over the course of 10 days. Melamine and cyanuric acid were administered together at 0%, 0.2%, 0.5%, and 1% to 1 cat per dose group. No effect on renal function was observed in cats fed with melamine or cyanuric acid alone. Cats dosed with a combination were euthanized at 48 hours after dosing because of acute renal failure. Urine and touch impressions of kidneys from all cats dosed with the combination revealed the presence of fan-shaped, birefringent crystals. Histopathologic findings were limited to the kidneys and included crystals primarily within tubules of the distal nephron, severe renal interstitial edema, and hemorrhage at the corticomedullary junction. The kidneys contained estimated melamine concentrations of 496 to 734 mg/kg wet weight and estimated cyanuric acid concentrations of 487 to 690 mg/kg wet weight. The results demonstrate that the combination of melamine and cyanuric acid is responsible for acute renal failure in cats. |
| 생태독성 수치 | LC50 Salmo gairdneri 1080 mg/L/96 hr. /Conditions of bioassay not specified in source examined/LC50 Pimephales promelas >2100 mg/L/96 hrstatic. /Conditions of bioassay not specified in source examined/LC50 Lepomis macrochirus 1400 mg/L/96 hr. /Conditions of bioassay not specified/LC50 Lepomis macrochirus >1000 mg/L/96 hrFor more Ecotoxicity Values (Complete) data for CYANURIC ACID (11 total), please visit the HSDB record page. |
| 환경 거동 | TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 58(SRC), determined from a water solubility of 2,593 mg/L(2) and a regression-derived equation(3), indicates that cyanuric acid is expected to have high mobility in soil(SRC). The pKa of cyanuric acid is 6.88(4), indicating that this compound will partially exist in the anion form in the environment and anions generally do not adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(5). Volatilization of cyanuric acid from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 8.74X10-15 atm-cu m/mole(SRC), using a fragment constant estimation method(6). Cyanuric acid is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 4.4X10-11 mm Hg(SRC), determined from a fragment constant method(7). Cyanuric acid biodegrades readily under a wide variety of natural conditions, and particularly well in systems of either low or zero dissolved- oxygen levels, such as anaerobic activated sludge and sewage, soils, muds, and muddy streams and river waters, as well as ordinary aerated activated sludge systems with typically low (1 to 3 ppm) dissolved-oxygen levels(8).AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 58(SRC), determined from a water solubility of 2,593 mg/L(2) and a regression-derived equation(3), indicates that cyanuric acid is not expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is not expected(3) based upon an estimated Henry's Law constant of 8.7X10-15 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). According to a classification scheme(5), BCF values of <0.5(6), suggest the potential for bioconcentration in aquatic organisms is low(SRC). Cyanuric acid biodegrades readily under a wide variety of natural conditions, and particularly well in systems of either low or zero dissolved- oxygen levels, such as anaerobic activated sludge and sewage, soils, muds, and muddy streams and river waters, as well as ordinary aerated activated sludge systems with typically low (1 to 3 ppm) dissolved-oxygen levels(7).ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), cyanuric acid, which has an estimated vapor pressure of 4.4X10-11 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), is expected to exist solely in the particulate phase in the ambient atmosphere. Particulate-phase cyanuric acid may be removed from the air by wet or dry deposition(SRC). Cyanuric acid does not absorb light at wavelengths >290 nm(4) and therefore is not expected to be susceptible to direct photolysis by sunlight(SRC). |
| 유해 작용 | Nephrotoxin - The chemical is potentially toxic to the kidneys in the occupational setting. |
| 노출 경로 | The substance can be absorbed into the body by inhalation. |
| 생태독성 발췌 | /PLANTS/ Very toxic to certain types of barley and radishes.. |
| Signs and Symptoms | Cough. Sore throat.Redness.Sore throat. Abdominal pain. |
| Soil Adsorption/Mobility | The Koc of cyanuric acid is estimated as 58(SRC), using a water solubility of 2,593 mg/L(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that cyanuric acid is expected to have high mobility in soil. The pKa of cyanuric acid is 6.88(4), indicating that this compound will partially exist in the anion form in the environment and anions generally do not adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(5). |
| Artificial Pollution Sources | Cyanuric acid's production and use as a convenient lab source of cyanic acid gas, in the preparation of melamine, sponge rubber, herbicides, dyes resins, antimicrobial agents and as a stabilizer and disinfectant in swimming pool water(1) may result in its release to the environment through various waste streams(SRC). Its former use as a herbicide(2) resulted in its direct release to the environment(SRC). |
| Environmental Biodegradation | AEROBIC: A study using a Warburg respirometer with acclimated sewage sludge and 100 mg cyanuric acid found that cyanuric acid was inhibitory to biodegradation(1). Another study using COD, TOC, and UV with activated sludge found no degradation with cyanuric acid even with acclimated sludge(2). Cyanuric acid completely degraded in a study using s-triazine herbicide production wastes, HPLC and mixed (aerobic and anaerobic) bacteria cultures(4). Biodegradation of cyanuric acid by aerated activated sludge ranges from 14% at 8.7 mg/L DO and 5 hours, to 100% at 2.5 mg/L DO and 10 hours(5). After 16 days, 87% of labeled cyanuric acid had evolved as 14-CO2 and after 192 days, the percentage had increased to 99% in grab samples of aerobic soils (cyanuric acid concN 2.5 ppm)(3). In grab samples of saturated soil, 83% of labeled cyanuric acid had evolved as 14CO2 after 66 days, and after 375 days, the percentage increased to 99% (cyanuric acid concN 2.5 ppm)(3).AEROBIC: Cyanuric acid biodegrades readily under a wide variety of natural conditions, and particularly well in systems of either low or zero dissolved- oxygen levels, such as anaerobic activated sludge and sewage, soils, muds, and muddy streams and river waters, as well as ordinary aerated activated sludge systems with typically low (1 to 3 ppm) dissolved-oxygen levels(1). For example: CO2 evolution from 14C-labeled cyanuric acid on soils, muds and in natural waters ranges from 1% at 8 days to 116% at 23 days at room temperature(1). Cyanuric acid is a biodegradation product of melamine when the latter is subjected to a biodegradation test using Pseudomonas strain A(2).ANAEROBIC: At a concentration of 10 ug/mL cyanuric acid in anaerobic sewage, cyanuric acid degraded by 25-50% in 48 hours, and 100% within 72-96 hours(1). In an anaerobic mixed liquor, CO2 evolution occurred at 4% within 7 hours, 11% in 17 hours, and 82% in 17 days(1). However, cyanuric acid exhibited 0% methane production following a one-year incubation in anoxic aquifer slurries(2).STUDIES WERE CONDUCTED IN GREENFIELD SANDY LOAM SOIL & IN PURE CULTURE. 87% OF LABELED CYANURIC ACID HAD EVOLVED AS (14)CO2 AFTER 16 DAYS INCR TO 96% AFTER 32 DAYS.For more Environmental Biodegradation (Complete) data for CYANURIC ACID (7 total), please visit the HSDB record page. |
| Environmental Bioconcentration | BCF values of <0.1 and <0.5 were derived for cyanuric acid at concentrations of 10 and 1 mg/L, respectively, and using orange-red killifish (Oryzias latipes) which were exposed over an 6-week period(1). According to a classification scheme(2), this BCF range suggests bioconcentration in aquatic organisms is low(SRC). |
| Volatilization from Water/Soil | The Henry's Law constant for cyanuric acid is estimated as 8.7X10-15 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that cyanuric acid is expected to be essentially nonvolatile from water surfaces(2). Cyanuric acid is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 4.4X10-11 mm Hg(SRC), determined from a fragment constant method(3). |
| 수질 위해 등급(WGK) | WGK 1 |
| TSCA 등재 상태 | TSCA listed |
| RTECS 번호 | XZ1800000 |
| 독성 | LD50 orally in rats: >5.00 g/kg (Canelli) |
| 관세 코드 | 29339900 |
| 기존화학 물질 | KE-33999 |
| 저장 분류 | 11 - Combustible Solids |
| 유해 물질 데이터 | 108-80-5(Hazardous Substances Data) |
용도
용도
Cyanuric acid is used in chemical synthesis (see Section 31.0), as an intermediate for chlorinated bleaches, as a selective herbicide, and as a whitening agent. The parent compound and salts, chlorinated salts, and chlorinated acids are used to disinfect swimming pools, restaurants, and barns. Chlorinated salts hydrolyze in water to form cyanurate and hypochlorous acid. Other monomeric isocyanurates (e.g., triallyl cyanurate) are used as cross-linking components for producing polyurethanes, polyesters, and alkyd resins. Tris (2-hydroxyethyl)isocyanurate is used in wire lacquers. Cyanuric acid is produced in the United States.
일반 설명
Crystals.
제조 및 합성 방법
생산 방법
Cyanuric acid is an odorless, crystalline powder. Chlorinated isocyanuratesareusuallypreparedbycontrolledchlorinationof the sodium or potassium salts of cyanuric acid. Other monomeric isocyanurates made from the parent compound include tris(2-hydroxyethyl)isocyanurate and triallyl cyanurate.