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HCID 7956作成日：2026年10月27日

シアヌル酸

シアヌル酸 · ヘキサヒドロ-1,3,5-トリアジン-2,4,6-トリオン · プソイドシアヌル酸 · 1,3,5-トリアジン-2,4,6-トリオール · s-トリアジン-2,4,6-トリオール · 2,4,6-トリヒドロキシ-1,3,5-トリアジン · イソシアヌル酸 · 1,3,5-トリアジン-2,4,6(1H,3H,5H)-トリオン

https://huagongshe.com/ja/chemical/7956

シアヌル酸 の分子構造式

識別子と物理属性

CAS No.108-80-5
分子式C3H3N3O3
平均分子量129.07 g/mol
単同位体質量129.01744096 g/mol
SMILESO=c1[nH]c(=O)[nH]c(=O)[nH]1
InChIKeyZFSLODLOARCGLH-UHFFFAOYSA-N
PubChem CID7956
ChEMBLCHEMBL243087
ChEBICHEBI:38028
EC No.203-618-0
DTXSIDDTXSID7024873
現地名シアヌル酸

化学・物理的性質

XLogP-1.2
極性表面積87.3
水素結合供与体数3
水素結合受容体数3
回転可能結合数0
重原子数9
形式電荷0
複雑度135
物質分類Nitrogen Compounds -> Triazines
PolymersPlastics -> Flame retardantsPlastics -> Polyolefin-IPolyolefin-II
pHpH of saturated aqueous solution @ room temperature = 4.83.8-4.0 (H2O, 20℃)(saturated solution)
臭いOdorlessオフホワイト結晶、無臭
味Slightly bitter
密度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 RetardantsFlame retardants
Color/FormWhite crystalline solidCRYSTALLINE POWDER
溶解度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.硫酸、ジメチルホルムアミド、水酸化ナトリウム、水酸化カリウム、ジメチルスルホキシドに可溶。アセトン、ベンゼン、エーテル、エタノール、ヘキサンに溶けにくい。冷メタノール、ベンゼン、クロロホルムに不溶。0.3g/100mL(25℃)
沸点DECOMPOSES (NTP, 1992)Sublimes and dissociates to isocyanuric acid at higher />330 °C/ temperatures74 °C
DecompositionThe 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.
融点greater than 680 °F (DEC.) (NTP, 1992)360 °C
蒸気圧<0.0001 Pa (25 °C)
屈折率1.4500 (estimate)
貯蔵条件Store below +30°C.
外観・状態結晶性粉末または塊
pKa（酸解離定数）6.88, 11.40, 13.5(at 25℃)
色ホワイトからライトベージュ
Merck14,2698
BRN126982
ヘンリー定数1.1×109 mol/(m3Pa) at 25℃, HSDB (2015)
安定性安定。強力な酸化剤とは相容れない。
InChI1S/C3H3N3O3/c7-1-4-2(8)6-3(9)5-1/h(H3,4,5,6,7,8,9)
InChIKeyZFSLODLOARCGLH-UHFFFAOYSA-N
SMILESO=C1NC(=O)NC(=O)N1
LogP（分配係数）-1.31 at 25℃
CAS データベース108-80-5(CAS DataBase Reference)
NISTの化学物質情報1,3,5-Triazine-2,4,6(1H,3H,5H)-trione(108-80-5)
EPAの化学物質情報Cyanuric acid (108-80-5)

化学的特性

white powder

化学性质

シアロンは以下のような多くの特性を持つことで知られています

安全性と法規制

GHS 分類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.
規制情報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
その他の安全情報IMAP assessments - 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione: Human health tier I assessment
火災危険Gives off irritating or toxic fumes (or gases) in a fire.
健康有害性SYMPTOMS: Symptoms of exposure to this compound include, local irritation of the eyes.
有害性の概要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]
反応性グループAmides and Imides
Special ReportsHammond 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.

用途

解説

2,4,6-trihydroxy-1,3,5-triazine．C3H3N3O3(129.07)．シアヌル酸は，三臭化シアヌルC3N3Br3の加水分解により生成する．"二水和物C3H3N3O3·2H2Oは風解性の無色の柱状結晶．固体状態でも溶液中でもケト-エノール平衡状態にあり，通常，ケト形が優先的に存在する．100 ℃ で脱水して無水物となる．無水和物は融点360 ℃ 以上で分解してシアン酸HOCNを生成する．熱水，熱エタノール，ピリジン，濃塩酸，硫酸に可溶，エーテル，アセトン，ベンゼンに難溶．シアン酸の発生源および選択的除草剤として用いられる．[CAS 108-80-5][別用語参照]三塩化シアヌル，シアヌル酸トリメチル森北出版「化学辞典（第2版）

用途

有機合成原料。消毒剤。シアンガス発生原料。

用途

シアロンの優れた物性は多くの応用分野へと広がっています以下にその主な用途を挙げます

用途

シアヌル酸はそのままで使用されることはほとんどなく、大半が塩素と反応させて塩素化シアヌル（トリクロロイソシアヌル酸）として使用される。塩素化シアヌルはプールなどの殺菌剤として使用される。 他の用途としては量は少ないが、各種中間体の原料、メラミンと反応させて、メラミンシアヌレートの原料などとして使用されている。

使用

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.

一般的な説明

Crystals.

使用用途

イソシアヌル酸はそのままで使用されることはほとんどなく、誘導体に変換されたのちに利用されています。イソシアヌル酸の誘導体のうち、工業的に利用されているものにはトリクロロイソシアヌル酸（塩素化イソシアヌル酸）やメラミンシアヌレートがあります。 1. 塩素化イソシアヌル酸 塩素化イソシアヌル酸は、イソシアヌル酸の水素原子をいくつか塩素原子で置換することで得られる物質で、3つ置換されたものはトリクロロイソシアヌル酸、2つ置換されたものはジクロロイソシアヌル酸という名称です。 塩素化イソシアヌル酸は白色の結晶性固体で、強い塩素臭を持っています。水溶性を高めるために、ナトリウム塩やカリウム塩の形で使用されることも多いです。 人間の体内の組織への蓄積性は低く、すぐ排泄されるため毒性は低いとされていますが、分解して塩化水素、次亜塩素酸、酸化窒素などの有害な気体を発生させる可能性があるため、保管には注意が必要です。殺菌剤以外の用途としては、有機化学実験における塩素化剤や、ウールの縮毛防止剤などがあります。 2. メラミンシアヌレート メラミンシアヌレートは、イソシアヌル酸とを反応させることで得られる物質です。メラニンとシアヌル酸が水素結合のみを介して塩を形成しており、両者の間に共有結合は形成されていません。水は溶けませんが、有機溶媒に分散しやすい性質を持っています。常温、常圧では結晶性の白色固体で、白色系の固体潤滑剤として使用されています。 また、熱による分解過程においてカーボンフォーム層が形成され、この層は熱と酸素を遮断する働きが見られます。ハロゲンを含んでおらず、分解の際にも煙がほとんど出ず、窒素や、アンモニアといった毒性の低い気体のみを発生させるため、環境にやさしい難燃剤として注目されています。常温の乾燥した環境で保存する必要があります。

使用用途

殺菌・漂白剤に使用される塩素化イソシアヌル酸 シアヌル酸は、主に塩素化イソシアヌル酸の原料として使用されています。塩素化イソシアヌル酸は、殺菌漂白効果に優れているため消毒・殺菌剤として幅広く使用されています。特に、生活用水および排水や、プールなどの消毒に用いられている物質です。 その他、シアン酸・シアンガスの発生源および選択的除草剤としての用途もあります。また、メラミンシアヌレートの原料として使用されたり、各種中間体の原料として使用されたりすることもあります。

製法・合成法

調製方法

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.

純化方法

It crystallises from water. Dry it at room temperature in a desiccator in a vacuum. [Beilstein 26 III/IV 632.]

FIFRA 要件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 ProfileAn 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)
大気基準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 DangersDecomposes at >320 °C. This produces toxic fumes including nitrogen oxides and isocyanic acid. Reacts with chlorine. This generates explosion hazard.
Air and Water ReactionsSoluble in hot water [Hawley].
消火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.
応急処置措置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.
応急処置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.
安全保管Dry. Well closed. Separated from chlorine.
消火手順Water spray, alcohol resistant foam, powder, carbon dioxide.
保管条件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...
清掃方法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.
非火災時の漏出対応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.
処分方法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.
漏出処分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 MeasuresImpervious 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 PreventionWear safety spectacles.
相互作用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.
生態毒性値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.
環境中動態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).
有害作用Nephrotoxin - The chemical is potentially toxic to the kidneys in the occupational setting.
暴露経路The substance can be absorbed into the body by inhalation.
生態毒性抜粋/PLANTS/ Very toxic to certain types of barley and radishes..
Signs and SymptomsCough. Sore throat.Redness.Sore throat. Abdominal pain.
Soil Adsorption/MobilityThe 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 SourcesCyanuric 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 BiodegradationAEROBIC: 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 BioconcentrationBCF 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/SoilThe 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).
水環境危害等級（WGK）WGK 1
TSCA 収載状態TSCA listed
RTECS 番号XZ1800000
毒性LD50 orally in rats: >5.00 g/kg (Canelli)
税関コード29339900
化審法(5)-1037, (5)-1038
貯蔵分類11 - Combustible Solids
有害物質データ108-80-5(Hazardous Substances Data)