1306-23-6[S]=[Cd]CJOBVZJTOIVNNF-UHFFFAOYSA-NCadmium sulfide is a cadmium molecular entity.
1306-23-6、68859-25-6CHEBI:50833Metals -> Cadmium Compounds, Inorganic
Carcinogens
Cubic structure: 4.50 g/cu cm; hexagonal structure: 4.82 g/cu cm
Density: 4.826 g/cu cm
4.8 g/cm³
4.83 @25 °C
Yellow-orange hexagonal crystals
Light-yellow or orange-colored cubic or hexagonal crystals.
Yellow or brown powder
Dimorphic, existing in the sphalerite (cubic) and wurtzite (hexagonal) crystal structures.
The log K(sp) (log solubility product constant) is 5.73
Soluble in acid
Soluble in concentrated or warm dilute mineral acids with evolution of H2S; readily decomposes or dissolved by moderately dilute HNO3.
Forms a colloid in hot water
Solutions of cadmium salts and H2S or Na2S yield a yellow precipitate in excess of Na2S
For more Solubility (Complete) data for CADMIUM SULFIDE (6 total), please visit the HSDB record page.
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Danger
H302: Harmful if swallowed [Warning Acute toxicity, oral]
P203, P260, P264, P270, P273, P280, P301+P317, P318, P319, P330, P405, and P501 (click each P-code to see the statement)
Danger
H301 (29.5%): Toxic if swallowed [Danger Acute toxicity, oral]
P203, P260, P264, P270, P271, P273, P280, P284, P301+P316, P301+P317, P304+P340, P316, P318, P319, P320, P321, P330, P391, P403+P233, P405, and P501 (click each P-code to see the statement)
Chemical: Cadmium sulfide (CdS)
Chemical: C.I. Pigment Yellow 37
Hazard Traits - Carcinogenicity
Cadmium sulfide (CdS) is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Cadmium sulfide (CdS) 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)
REACH registered substance: Cadmium sulphide (EC: 215-147-8)
Restricted substance: Cadmium sulphide
Evaluation - Cadmium sulfide pigments
Evaluation - Cadmium sulfide pigments
An irritant; May cause effects on the kidneys, bones, and respiratory tract; [ICSC] An irritant; Cadmium compounds are potential carcinogens that are toxic to the kidneys, liver, and respiratory tract. The heavy metal sulfides are generally insoluble and show little toxic action except through the liberation of hydrogen sulfide. [MSDSonline] See Cadmium and the linked diseases.
The major hazards encountered in the use and handling of cadmium sulfide stem from its toxicologic properties. Toxic primarily by ingestion and inhalation, exposure to this yellow, orange, red, or brown crystalline substance may occur from its use as a pigment for coloring glass, soaps, textiles, paper, rubber, inks, ceramic glazes, fireworks, and epoxy resins. Effects from exposure may include headache, shortness of breath, chest pain, kidney damage, liver damage, emphysema, chronic bronchitis, and pulmonary edema (possibly resulting in death). Processes and operations which may release cadmium fumes or dust should be enclosed and fitted with exhaust ventilation. In activities where over-exposure is possible, workers should wear a high efficiency particulate filter respirator or self-contained breathing apparatus. Protective clothing also should be worn. Preferably this should include disposable one piece suits (close-fitting at the ankles and wrists), gloves, hair covering, and overshoes. These should be removed before leaving work. If contact should occur, immediately wash contaminated skin with large amounts of water. Do not eat, smoke, or drink in work areas. Cadmium sulfide presents only a moderate fire hazard (when in the form of dust) if exposed to heat, flame, or by chemical reaction with oxidizing agents, metals, hydrogen azide, zinc, selenium, or tellurium. Wear a self-contained breathing apparatus when fighting such fires. Cadmium sulfide should be stored in cool, well-ventilated areas, out of direct rays of sun, and away from combustibles and other fire hazards. Should hazardous concentrations of cadmium sulfide are accidentally released, remove all ignition sources, ventilate the area, and collect the released material in closed containers for disposal. Before implementing land disposal of waste cadmium sulfide, consult environmental regulatory agencies for guidance.
/The objective of this study was/ to fully understand the cytotoxicity of after-degradation /quantum dots/ (QDs)...Biomimetic method was proposed to synthesize cadmium sulfide (CdS) QDs. Thereafter MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide) assay was conducted to evaluate their cytotoxicity. ...toxicity mechanism /was studied using/ intracellular reactive oxygen species (ROS) measurement with /dichlorodihydrofluorescein diacetate/ DCFH-DA, glutathione (GSH) measurement with /5,5'-dithio-bis(2-nitrobenzoic acid); Ellman reagent/ DTNB, and cellular cadmium assay using atomic absorption spectrometer. Microsized CdS were simultaneously tested as a comparison. MTT assay results indicated that CdS QDs are more toxic than microsized CdS especially at concentrations below 40 ug/mL. While microsized CdS did not trigger ROS elevation, CdS QDs increase ROS by 20-30% over control levels. However, they both deplete cellular GSH significantly at the medium concentration of 20 ug/mL. In the presence of /N-acetyl cysteine/ NAC, cells are partially protected from CdS QDs, but not from microsized particles. Additionally, nearly 20% of cadmium was released from CdS nanoparticles within 24 hr, which also accounts for QDs' toxicity. Intracellular ROS production, GSH depletion, and cadmium ions (Cd(2+)) release are possible mechanisms for CdS QDs' cytotoxicity. .../It is/ also suggested that with QD concentration increasing, the principal toxicity mechanism changes from intracellular oxidative stress to Cd(2+) release.
Cadmium is absorbed from oral, inhalation, and dermal routes. Cadmium initially binds to metallothionein and albumin and is transported mainly to the kidney and liver. Toxic effects are observed once the concentration of cadmium exceeds that of available metallothionein, and it has also been shown that the cadmium-metallothionein complex may be damaging. Cadmium is not known to undergo any direct metabolic conversion and is excreted unchanged, mainly in the urine. (L6)
AFTER A YR OF FEEDING 1 PPM CADMIUM (AS CADMIUM SULFIDE (CDS) OR CD CONTAINED IN ROLL SHELL LIVER) IN CA DEFICIENT DIET OF FEMALE RATS, ACCUM RATE IN LIVER & KIDNEY WAS 0.33-0.48%, WHEREAS THAT OF WATER SOL CD CMPD & CD FED AS CD POLLUTED RICE WAS 0.43-0.57%.
Rats were exposed 6 hr/day over 10 days to 0.3 mg/cu m of water soluble cadmium chloride and 0.2, 1.0 and 8.0 mg/cu m of insoluble cadmium sulfide, then killed at intervals over a 3-month period for serial measurements of lung, renal and fecal cadmium. Cadmium chloride and high-dose cadmium sulfide animals showed a transient increase in lung weight. Clearance of both compounds was biphasic. Approximately 40% of deposited material was cleared during the 10-day exposure period. For cadmium chloride, only 9% of the lung burden was cleared rapidly after the last exposure (half-life 1.0 days) and 47%. slowly (half-life 87 days), leaving a residual lung burden of 44%. For cadmium sulfide, 41% of the lung burden was cleared rapidly (half-life 1.4 days) and 40% slowly (half-life 42 days), leaving a final residue 19%. In the cadmium sulfide high-dose group, the retention of cadmium sulfide in the lung was greater than that in the cadmium sulfide low-dose groups, indicating that clearance mechanisms may possibly have been impaired in the high-dose group by too great a lung burden. For both compounds, fecal cadmium was initially high. Renal accumulation of cadmium was substantial for cadmium chloride during the exposure period and continued over the following months until it represented approximately 35% of the total cadmium cleared from the lung. For cadmium sulfide, renal accumulation was only 1% of the amount cleared from the lung. The bioavailability of cadmium from cadmium sulfide is thus poor, the majority being cleared from the lungs and excreted in the feces. However, the bioavailability of inhaled cadmium sulfide measured as cadmium in the kidney is greater than the bioavailability of orally ingested cadmium sulfide.
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Wet Solid
Yellow or brown solid; Forms a colloid in hot water; [Hawley] Light yellow or orange solid; [Merck Index] Yellow odorless pieces; [MSDSonline]
LIGHT YELLOW OR ORANGE CRYSTALS OR YELLOW-TO-BROWN POWDER.
Can be polished like a metal. It is an n-type semiconductor.
beta-Cadmium sulfide can be transformed to alpha-cadmium sulfide by heating at 750 °C in a sulfur atmosphere.
Sublimes at 980 °C
Oxidized to the sulfate, basic sulfate and eventually the oxide on heating in air to 700 °C, especially in the presence of moisture.
log Ksp = -14.36 at 25 °C and 1 atm. (This value was determined for long equilibrium times and is as much as 2 orders of magnitude for published values for fresh precipitates.)
Cadmium sulfide is an odorless, crystalline, lemon yellow to orange solid.
National Toxicology Program. Eleventh Report on Carcinogens (2005). The Report on Carcinogens is an informational scientific and public health document that identifies and discusses substances (including agents, mixtures, or exposure circumstances) that may pose a carcinogenic hazard to human health. Cadmium and Cadmium Compounds are listed as known to be human carcinogens. /Cadmium and Cadmium Compounds/[Available from, as of July 31, 2009: http://ntp.niehs.nih.gov/ntp/roc/eleventh/profiles/s028cadm.pdf]
D006; A solid waste containing cadmium may or may not become characterized as a hazardous waste when subjected to the Toxicity Characteristic Leaching Procedure listed in 40 CFR 261.24, and if so characterized, must be managed as a hazardous waste. /Cadmium/
Listed as a hazardous air pollutant (HAP) generally known or suspected to cause serious health problems. The Clean Air Act, as amended in 1990, directs EPA to set standards requiring major sources to sharply reduce routine emissions of toxic pollutants. EPA is required to establish and phase in specific performance based standards for all air emission sources that emit one or more of the listed pollutants. Cadmium sulfide is included on this list.
/GUIDE 154: SUBSTANCES - TOXIC AND/OR CORROSIVE (NON-COMBUSTIBLE)/ First Aid: Move victim to fresh air. Call 911 or emergency medical service. Give artificial respiration if victim is not breathing. Do not use mouth-to-mouth method if victim ingested or inhaled the substance; give artificial respiration with the aid of a pocket mask equipped with a one-way valve or other proper respiratory medical device. Administer oxygen if breathing is difficult. Remove and isolate contaminated clothing and shoes. In case of contact with substance, immediately flush skin or eyes with running water for at least 20 minutes. For minor skin contact, avoid spreading material on unaffected skin. Keep victim warm and quiet. Effects of exposure (inhalation, ingestion or skin contact) to substance may be delayed. Ensure that medical personnel are aware of the material(s) involved and take precautions to protect themselves. /Cadmium compound/
/GUIDE 154: SUBSTANCES - TOXIC AND/OR CORROSIVE (NON-COMBUSTIBLE)/ Spill or Leak: ELIMINATE all ignition sources (no smoking, flares, sparks or flames in immediate area). Do not touch damaged containers or spilled material unless wearing appropriate protective clothing. Stop leak if you can do it without risk. Prevent entry into waterways, sewers, basements or confined areas. Absorb or cover with dry earth, sand or other non-combustible material and transfer to containers. DO NOT GET WATER INSIDE CONTAINERS. /Cadmium compound/
/GUIDE 154: SUBSTANCES - TOXIC AND/OR CORROSIVE (NON-COMBUSTIBLE)/ Fire: Small fires: Dry chemical, CO2 or water spray. Large fires: Dry chemical, CO2, alcohol-resistant foam or water spray. Move containers from fire area if you can do it without risk. Dike fire control water for later disposal; do not scatter the material. Fire involving tanks or car/trailer loads: Fight fire from maximum distance or use unmanned hose holders or monitor nozzles. Do not get water inside containers. Cool containers with flooding quantities of water until well after fire is out. Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank. ALWAYS stay away from tanks engulfed in fire. /Cadmium compound/
/GUIDE 154: SUBSTANCES - TOXIC AND/OR CORROSIVE (NON-COMBUSTIBLE)/ Evacuation: ... Fire: If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions. /Cadmium compound/
For more DOT Emergency Guidelines (Complete) data for CADMIUM SULFIDE (8 total), please visit the HSDB record page.
Fresh air, rest.
Remove contaminated clothes. 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. Give one or two glasses of water to drink.
Biological Exposure Indices (BEI) [ACGIH] - Cd in urine = 5 ug/g creatinine; Cd in blood = 5 ug/L; sampling time not critical; Monitoring in blood should be preferred during the initial year of exposure and whenever changes in the degree of exposure are suspected. [ACGIH]
If material on fire or involved in fire: Extinguish fire using agent suitable for type of surrounding fire. (Material itself does not burn or burns with difficulty.) Use water in flooding quantities as fog. Use "alcohol" foam, dry chemical or carbon dioxide. /Cadmium compounds, NOS/
Generators of waste (equal to or greater than 100 kg/mo) containing this contaminant, EPA hazardous waste number D006, must conform with USEPA regulations in storage, transportation, treatment and disposal of waste.
Generators of waste (equal to or greater than 100 kg/mo) containing this contaminant, EPA hazardous waste number D006, must conform with USEPA regulations in storage, transportation, treatment and disposal of waste. /Cadmium/
SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.
Personal protection: particulate filter respirator adapted to the airborne concentration of the substance. Do NOT let this chemical enter the environment. Sweep spilled substance into covered containers. If appropriate, moisten first to prevent dusting. Carefully collect remainder. Then store and dispose of according to local regulations.
SRP: Contaminated protective clothing should be segregated in such a manner so that there is no direct personal contact by personnel who handle, dispose, or clean the clothing. Quality assurance to ascertain the completeness of the cleaning procedures should be implemented before the decontaminated protective clothing is returned for reuse by the workers. All contaminated clothing should not be taken home at end of shift, but should remain at employee's place of work for cleaning.
LC50; Species: Daphnia magna (Water flea) age <24 hr neonate; Conditions: freshwater, static, pH 7.5-9.1; Concentration: 11 ug/L for 48 hr
LC50; Species: Pimephales promelas (Fathead Minnow) age <24 hr neonate; Conditions: freshwater, static, pH 7.5-9.1; Concentration: 108 ug/L for 96 hr
The substance can be absorbed into the body by inhalation of its aerosol and by ingestion.
Oral (L6) ; inhalation (L6) ; dermal (L6)
Cadmium initially binds to metallothionein and is transported to the kidney. Toxic effects are observed once the concentration of cadmium exceeds that of available metallothionein, and it has also been shown that the cadmium-metallothionein complex may be damaging. Accumulation of cadmium in the kidney results in increased excretion of vital low and high weight molecular proteins. Cadmium is a high affinity zinc analog and can interfere in its biological processes. It also binds to and activates the estrogen receptor, likely stimulating the growth of certain types of cancer cells and causing other estrogenic effects, such as reproductive dysfunction. Cadmium causes cell apoptosis by activating mitogen-activated protein kinases. (L8, A18, A19, A28)
/AQUATIC SPECIES/ The toxicity of chemicals in sediments is influenced by the extent that chemicals bind to the sediment. It is shown that acid volatile sulfide (AVS) is the sediment phase that determines the LC50 for cadmium in the marine sediments tested. Although it is well known that metals can form insoluble sulfides, it apparently has not been recognized that AVS is a reactive pool of solid phase sulfide that is available to bind with metals. Amphipod sediment toxicity tests were conducted in the laboratory and the observed amphipod LC50s on a normalized cadmium concentration basis, [Cd]/[AVS], is the same for sediments with over an order of magnitude difference in dry weight normalized cadmium LC50s. Because other toxic metals also form insoluble sulfides, it is likely that AVS is important in determining their toxicity in sediments as well. Most freshwater and marine sediments contain sufficient acid volatile sulfide for this phase to be the predominant determinant of toxicity. The other sorption phases are expected to be important only for low AVS sediments, for example, fully oxidized sediments. From the point of view of sediment quality criteria the other sorption phases would be important for metals with large partition coefficients and large chronic water quality criteria.
Cough.
Redness. Pain.
Diarrhoea. Nausea.
Acute inhalation of cadmium fumes results in metal fume fever, which is characterized by chills, fever, headache, weakness, dryness of the nose and throat, chest pain, and coughing. Ingestion of cadmium causes vomiting and diarrhea. (L6)
Cadmium sulfide (CAS # 1306-23-6; 10% in 0.5% Jaguar) was evaluated for acute oral toxicity in groups of rats (8/sex/group) exposed by oral gavage to doses ranging from 1600 to 3200 mg/kg. Treatment was associated with no mortality, slight weakness, rough coats, and light-colored feces. On necropsy, gross changes in males included flaccid and more liquid testes with congested pin-point vessels. The authors reported an oral LD50 in rats greater than 3200 mg/kg.
/Occurs in/ a greenockite (cadmium sulfide) ore containing zinc sulfide ...
Cadmium compounds are naturally occurring, albeit relatively rare, and are widely distributed in the earth's crust; crustal abundance is between 0.1 and 0.5 ppm(1,2). Several minerals of cadmium have been identified, the most common of which is greenockite, CdS(2). Cadmium is usually found in zinc ores in which the CdS crystals are isomorphic to the zinc mineral sphalerite, ZnS(2).
D006; A solid waste containing cadmium may or may not become characterized as a hazardous waste when subjected to the Toxicity Characteristic Leaching Procedure listed in 40 CFR 261.24, and if so characterized, must be managed as a hazardous waste. /Cadmium/
Listed as a hazardous air pollutant (HAP) generally known or suspected to cause serious health problems. The Clean Air Act, as amended in 1990, directs EPA to set standards requiring major sources to sharply reduce routine emissions of toxic pollutants. EPA is required to establish and phase in specific performance based standards for all air emission sources that emit one or more of the listed pollutants. Cadmium sulfide is included on this list.
(AZ) ARIZONA 5 ug/L /Cadmium/
(ME) MAINE 3.5 ug/L /Cadmium/
(MN) MINNESOTA 4 ug/L /Cadmium/
Used as a pigment (plastics, paints, soaps, rubber, paper, glass, printing inks, ceramic glazes, textiles, and fireworks) and in phosphors, fluorescent screens, scintillation counters, semiconductors, photoconductors, solar cells, photomultipliers, radiation detectors, thin-film transistors, diodes/rectifiers, electron-beam pumped lasers, and smoke detectors; Also used to stabilized high-density polyethylene and in lead sealing glass binders; [HSDB] Occurs naturally in greenockite; [Ullmann]
Semiconductor Manufacturing [Category: Industry]
Ceramics making [Category: Hobbies]
Fluorescent screens, scintillation counters, rectifiers, photoconductor in xerography, transistors, photovoltaic cells, catalyst in photodecomposition of hydrogen sulfide
The hydrated bromide is prepared by dissolution of cadmium carbonate, oxide, sulfide, or hydroxide in hydrobromic acid. /Hydrated cadmium bromide/
As a pigment being fast to light and not affected by H2S; coloring glass yellow
2023: 1,113,825 lb
(1961) 1.52X10+9 GRAMS
Year, cadmium sulfide production in tons of cadmium content: 1984, 771; 1985, 477; 1986, 645; 1987, 540; 1988, 345; 1989, 267; 1990; 228.
The production of cadmium pigments is decreasing steadily as of the mid-1990s. In 1993, production was estimated to be anywhere between 1500 and 5000 metric tons. The reasonable projection for 1994 seems to be around 2000 metric tons, representing about one-third of the 1990 production. /Cadmium pigments/
Cadmium sulfide can be prepared by the reaction between hydrogen sulfide and cadmium vapor at 800 °C, or by heating a mixture of cadmium or cadmium oxide with sulfur. Usually, the sulfides are precipitated from aqueous solutions of cadmium salts by adding hydrogen sulfide or a soluble sulfide such as sodium sulfide.
A simple method involves treatment of an acidic or neutral cadmium ion solution with H2S or Na2S and collection of the dense yellow precipitate ... At room temperature one obtains yellow solids whereas from boiling solutions one obtains yellow solids at neutral pH but reddish solids at low pH.
(1) By passing hydrogen sulfide gas into a solution of a cadmium salt acidified with hydrochloric acid. The precipitate is filtered and dried.
Grade: Technical, NF, highpurity (single crystals).
Cadmium sulfide - purities: > 98-99.999%; phosphor (luminescent) grade, 99.99-99.999%
Pigment Yellow 37, CI 77199 (CdS)
Pigment Yellow 35, CI 77117 (cadmium sulfide lithopone: CdS/ZnS/BaSO4, CdS/BaSO4)
For more Formulations/Preparations (Complete) data for CADMIUM SULFIDE (7 total), please visit the HSDB record page.
Primary Metal Manufacturing
Cadmium sulfide (CdS): ACTIVE
A pure inorganic photoconductor has been developed consisting of uniform arrays of hexagonal microcrystallites of cadmium sulfide, each about 70 nm in diameter. These are produced by a sputtering process and are layered in a thin coat approximately 350 nm thick. They sustain a uniform charge of about 30 V. Each crystallite ... /acts/ like an independent photodiode. Coated on a substrate, such layer serves as a panchromatic film, suitable for high-resolution.
Occurs in nature as the mineral greenockite.
Cadmium sulfide may be prepared in color ranging from white to deep orange-red depending on the preparative method and resultant particle size of the material. The smaller the particle size the lighter the coloration and glass colored with cadmium sulfide is colorless when first cast from the melt where the particle size of the cadmium sulfide is less than 2 nm. Upon annealing at 700 °C, yellow-orange color develops as the particle size increases as a result of aggregation in the glass matrix.
Cadmium pigments are expensive and, where applicable, the lithopone forms are used. Lithopones are the concentrated pigments prepared with coprecipitated barium sulfate which acts as an extender. Lithopones contain ca 40 wt% concentrated pigment and ca 60 wt% barium sulfate.
출처Cadmium sulfide occurs in nature as the mineral greenoktite. The compound is widely used in pigments for paints, baking enamels, ceramics and plastics. It imparts bright yellow to maroon, with strong retention of color and resistance to alkalis. It also is used in inks, phosphors, and fluorescent screens. Other applications of this compound are in photovoltaic and solar cells (for converting solar energy to electrical energy), photoconductors (in xerography), thin film transistors and diodes, rectifiers, scintillation counters, pyrotechnics, and smoke detectors.
역사The discovery of cadmium sulphide is linked to that of the element cadmium. In 1817, the German chemist Friedrich Stromeyer, while examining samples of zinc carbonate, observed that upon heating, they turned yellow rather than the white colour expected for pure zinc oxide. Through further investigation, he isolated a new metal oxide and identified the presence of a previously unknown element, cadmium, associated with the zinc compounds.
용도cadmium sulfide is used as a colorant for paints and rubber; cadmium acetate is used in the production of craftware.
일반 설명Natural occurrence: hawleyite (structural type of sphalerite) and greenockite (structural type of wurtzite)
생산 방법Cadmium sulfide may be prepared by the reaction between hydrogen sulfide and cadmiumvapor at 800 Cor by heating a mixture of cadmium or cadmium oxide with sulfur.
Cadmium sulfide may be prepared by precipitation from an aqueous solution of its soluble salts such as cadmium chloride or cadmium nitrate by passing hydrogen sulfide. The reactions may be carried out in acidic, neutral or alkaline solutions using various cadmium salts to obtain different crystal modifications as shown in the table below. Cadmium sulfide also may be obtained by treatment of sodium or other alkali metal sulfide solution with that of a soluble cadmium salt. The compound also may be prepared by heating a mixture of cadmium or its oxide with sulfur at 800°C; or by the reaction of H2S with cadmium vapor at 800°C.