Basic information
- Standard SMILES
[Na+].[Na+].[S-2]- InChIKey
GRVFOGOEDUUMBP-UHFFFAOYSA-N- Molecular formula
- Na2S
- Average molar mass
- 78.05 g/mol
- Monoisotopic mass
- 77.95160956
Overview
Sodium sulfide, anhydrous is a yellow to brick red crystalline mass or fused solid with an odor of rotten eggs. If exposed to moist air it is liable to spontaneous heating and may cause ignition of nearby combustible material. It absorbs moisture from the air.
Names & identifiers
- Preferred name
- Sodium Sulfide
- IUPAC
- disodium;sulfide
- English name
- Sodium sulfide
- Molecular formula
- Na2S
- Molecular weight
- 78.04
Names & synonyms
Show more names
Database identifiers
- CAS
1313-82-2- PubChem CID
- 14804
- DTXSID
DTXSID0029636- ChEMBL
CHEMBL2107611- ChEBI
CHEBI:76208- UNII
- YGR27ZW0Y7
Properties
Computed structural properties
- Topological polar surface area
- 1 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 1
- Rotatable bonds
- 0
- Heavy atoms
- 3
- Formal charge
- 0
- Complexity
- 0
Experimental & physicochemical properties
Chemical Classes
Other Classes -> Sulfur Compounds
Corrosives
Density
1.856 at 68 °F (USCG, 1999) - Denser than water; will sink
1.856 @ 14 °C/4 °C
1.86 g/cm³
1.856 @25 °C
Color/Form
CLEAR CRYSTALS; YELLOW OR BRICK-RED LUMPS OR FLAKES
CUBIC CRYSTALS OR GRANULES
AMORPHOUS, YELLOW-PINK OR WHITE CRYSTALS
Yellow or brick-red lumps or flakes or deliquescent crystals.
White to pink, crystalline solid.
Solubility
Slightly soluble in alcohol; insoluble in ether.
Solubility in water (g/100 g water): 8.1 (-9.0 °C); 12.4 (0 °C); 18.6 (20 °C); 29.0 (40 °C); 35.7 (48 °C); 39.0 (50 °C).
Decomposition
When heated to decomp ... emits toxic fumes of /sulfur oxides and disodium oxide/.
920-950 °C
Melting Point
1180 °C (IN VACUO)
1172 °C
Physicochemical properties
- Melting point
- 950 °C · 950 °C(lit.)
- Density
- 1.86 g/mL · 1.86 g/mL at 25 °C(lit.)
- storage temp.
- Refrigerator (+4°C)
- solubility
- 2 O: · H2O: 0.1 g/mL, clear, colorless
- form
- flakes
- color
- Yellow
- Specific Gravity
- 1.856 · 1.856
- Odor
- Rotten egg odor
- Water Solubility
- 186 g/L · 186 g/L (20 ºC)
- Sensitive
- Hygroscopic
- Crystal Structure
- 2 type · Reverse CaF2 type
- crystal system
- Cube
- Merck
- 14 · 14,8681
- Space group
- 3 m · Fm3m
- Lattice constant
- a/nm
- Symbol(GHS)
- 5 · GHS05,GHS06,GHS09
- Signal word
- Danger
- Hazard statements
- 302 · H302-H311-H314-H400
- Precautionary statements
- 264 · P264-P270-P280-P260-P273-P301+P312-P330-P302+P352-P312-P361+P364-P301+P330+P331-P303+P361+P353-P363-P304+P340-P310-P305+P351+P338-P391-P405-P501
- PPE
- 3 · Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
- Hazard Codes
- C,N,Xn
- Risk Statements
- 31 · 31-34-50-22
- Safety Statements
- 26 · 26-45-61-36/37/39
- RIDADR
- 1385 · UN 1385 4.2/PG II (SODIUM SULPHIDE, ANHYDROUS or SODIUM SULPHIDE with less than 30 % water of crystallization)
- WGK Germany
- 2 · 2
- RTECS
- 1905000 · WE1905000
- F
- 3 · 3-8-9-23
- TSCA
- TSCA listed
- HazardClass
- 4.2 · 4.2
- PackingGroup
- II
- HS Code
- 28301010 · 28301010
- Storage Class
- 4.2 · 4.2 - Pyrophoric and self-heating hazardous materials
- Hazard Classifications
- 3 DermalAcute · Acute Tox. 3 DermalAcute Tox. 3 OralAquatic Acute 1Eye Dam. 1Met. Corr. 1Self-heat. 1Skin Corr. 1B
- Hazardous Substances Data
- 1313 · 1313-82-2(Hazardous Substances Data)
- REACH Registrations
- Active
- Excepted Quantities
- Max Inner Pack (30g or 30ml) and Max Outer Pack (500g or 500ml)
Safety & regulation
GHS classification
GHS Classification
Danger
H302: Harmful if swallowed [Warning Acute toxicity, oral]
P260, P262, P264, P270, P273, P280, P301+P317, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P330, P361+P364, P363, P391, P405, and P501 (click each P-code to see the statement)
Hazard information
Fire Hazards
Special Hazards of Combustion Products: Irritating sulfur dioxide is produced in fire. (USCG, 1999)
· Combustible material: may burn but does not ignite readily.
· Flammable/combustible material.
Combustible. Gives off irritating or toxic fumes (or gases) in a fire.
Fire Potential
MOIST SODIUM SULFIDE IS SPONTANEOUSLY FLAMMABLE UPON DRYING IN AIR.
Combustible solid.
Health Hazards
Caustic action on skin and eyes. If ingested may liberate hydrogen sulfide in stomach. (USCG, 1999)
· TOXIC and/or CORROSIVE; inhalation, ingestion or skin contact with material may cause severe injury or death.
· Fire will produce irritating, corrosive and/or toxic gases.
Hazards Summary
Hydrogen sulfide released slowly when exposed to moist air and rapidly when exposed to acids; Sulfur oxides and hydrogen sulfide may be generated during a fire; Corrosive to the eyes and skin; [CHEMINFO] Corrosive; Inhalation of high concentration can cause chemical pneumonitis; [MSDSonline] See Hydrogen sulfide.
DOT ID and Guide
1849 153
1385 135
Reactivity Profile
SODIUM SULFIDE is a white to yellow crystalline material, flammable. Can explode on rapid heating or when shocked. Violent reaction with carbon, charcoal, diazonium salts, N,N-dichloromethylamine, strong oxidizers, water. On contact with acids it liberates highly toxic and flammable hydrogen sulfide gas. When heated to decomposition it emits toxic fumes of sodium oxide, and oxides of sulfur [Bretherick, 5th ed., 1995, p. 1729].
Safety & protection
Fire Fighting
Excerpt from ERG Guide 135 [Substances - Spontaneously Combustible]:
Use water in large amounts, water spray, foam, dry powder.
First Aid Measures
Fresh air, rest. Refer for medical attention.
First rinse with plenty of water for at least 15 minutes, then remove contaminated clothes and rinse again. Refer for medical attention .
First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Do NOT induce vomiting. Give one or two glasses of water to drink. Refer for medical attention .
Accidental Release Measures
· CALL 911. Then call emergency response telephone number on shipping paper. If shipping paper not available or no answer, refer to appropriate telephone number listed on the inside back cover.
· ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.
· CALL 911. Then call emergency response telephone number on shipping paper. If shipping paper not available or no answer, refer to appropriate telephone number listed on the inside back cover.
· ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.
First Aid
INGESTION: give water; induce vomiting; call a doctor.
General First Aid:
General First Aid:
Exposure Control and Personal Protection
· Wear positive pressure self-contained breathing apparatus (SCBA).
· Wear positive pressure self-contained breathing apparatus (SCBA).
Fire Fighting Procedures
Approach fire from upwind to avoid hazardous vapors & toxic decomp products. Use flooding quantities of water. Do not use carbon dioxide.
Flood with water. /sodium sulfide, anhydrous or sodium sulfide; sodium sulfide, hydrated with not less than 30% water/
Extinguish fire using agent suitable for type of surrounding fire. Material itself does not burn or burns with difficulty. Use dry chemical, dry sand, or carbon dioxide. If large quantities of combustibles are involved, use water in flooding quantities as spray and fog. Use water spray to knock-down vapors. Keep run-off water out of sewers and water sources./sodium sulfide solutions containing sodium hydrosulfide; sodium sulfide solutions containing sodium hydroxide/
Cleanup Methods
Approach release from upwind. Keep water away from release. Prompt cleanup & removal are necessary. Shovel dry material into suitable dry container. Control runoff & isolate discharged material for proper disposal.
The catalyst activities for Na2S oxidation in aqueous soln were examined for various materials such as activated C, C black, ferric salts, hydroquinone, 1,4-naphthoquinone-2-sulfonic acid sodium salt, 1,4-naphthoquinone and their mixed systems. These catalyst systems are all active and, applied to wastewater and sludge treatments, gave good results.
Disposal Methods
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.
Spillage Disposal
Remove all ignition sources. Cover the spilled material with dry earth or sand. Sweep spilled substance into covered containers. Carefully collect remainder. Then store and dispose of according to local regulations. Do NOT let this chemical enter the environment. Personal protection: chemical protection suit including self-contained breathing apparatus.
Toxicology
Signs and Symptoms
Cough. Burning sensation. Laboured breathing. Shortness of breath. Sore throat.
Redness. Pain. Skin burns. Blisters.
Redness. Pain. Blurred vision. Severe deep burns.
Abdominal pain. Burning sensation. Shock or collapse.
Human Toxicity Excerpts
...SODIUM SULFIDE MAY PRODUCE CAUSTIC BURNS...
CONTACT OF SODIUM SULFIDE WITH WORKMEN'S EYES HAS BEEN NOTED TO CAUSE BURNS WHICH MAY BE SLOW HEALING, OWING PRESUMABLY TO STRONG ALKALINITY.
IF FREE GASTRIC ACIDITY IS HIGH, INGESTION...MAY RESULT IN...DECOMP TO HYDROGEN SULFIDE IN STOMACH, WITH SUBSEQUENT SYSTEMIC POISONING. IN ANY CASE ALKALINE SULFIDES ARE STRONG LOCAL IRRITANTS TO MUCOUS MEMBRANE (& SKIN). /SULFIDE SALTS/
SOME OF SYMPTOMS ASSOC WITH SODIUM SULFIDE INTOXICATION MAY BE ATTRIBUTABLE TO HYDROGEN SULFIDE RELEASED IN STOMACH.
For more Human Toxicity Excerpts (Complete) data for SODIUM SULFIDE (6 total), please visit the HSDB record page.
Antidote and Emergency Treatment
For advanced treatment: Consider orotracheal or nasotracheal intubation for airway control in the patient who is unconscious or in respiratory arrest. Positive-pressure ventilation techniques with a bag-valve-mask device may be beneficial. Monitor cardiac rhythm and treat arrhythmias if necessary ... . Start an IV with D5W TKO /SRP: To keep open, "minimal flow rate"/. Use lactated Ringer's if signs of hypovolemia are present. Watch for signs of fluid overload. Consider drug therapy for pulmonary edema ... . For hypotension with signs of hypovolemia, administer fluid cautiously. Watch for signs of pulmonary edema. Consider vasopressors to treat hypotension without signs of hypovolemia ... . Treat seizures with diazepam (Valium) ... . In severe cases use amyl nitrite and sodium nitrite ... as described for cyanide poisoning; omit the sodium thiosulfate injection. Early administration will be the most effective. DIRECT PHYSICIAN ORDER ONLY ... . Use proparacaine hydrochloride to assist eye irrigation ... . For basic treatment: Establish a patent airway. Suction if necessary. Watch for signs of respiratory insufficiency and assist ventilations if necessary. Administer oxygen by nonrebreather mask at 10 to 15 L/min. Monitor for pulmonary edema and treat if necessary ... . Monitor for shock and treat if necessary ... . Anticipate seizures and treat if necessary ... . For eye contamination, flush eyes immediately with water. Irrigate each eye continuously with normal saline during transport ... . Treat with rapid rewarming techniques ... if frostbite occurs. /Hydrogen sulfide and related compounds/
Non-Human Toxicity Values
LD50 Rat oral 208 mg/kg
LD50 Rat ipr 147 mg/kg
LD50 Mouse oral 205 mg/kg
Safety data
- F
- 3-8-9-23
- PPE
- Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
- wgk
- 2
- tsca
- TSCA listed
- rtecs
- WE1905000
- ridadr
- UN 1849 8/PG II (SODIUM SULPHIDE, HYDRATED with not less than 30 % water)
- hs_code
- 28301010
- risk_code
- 31-34-50-22
- Signal word
- Danger
- Symbol(GHS)
- GHS05,GHS06,GHS09
- hazard_code
- C,N,Xn
- safety_code
- 26-45-61-36/37/39
- hazard_class
- 4.2
- Storage Class
- 4.2 - Pyrophoric and self-heating hazardous materials
- packing_group
- II
- Hazard statements
- H302-H311-H314-H400
- Excepted Quantities
- Max Inner Pack (30g or 30ml) and Max Outer Pack (500g or 500ml)
- REACH Registrations
- Active
- Hazard Classifications
- Acute Tox. 3 DermalAcute Tox. 3 OralAquatic Acute 1Eye Dam. 1Met. Corr. 1Self-heat. 1Skin Corr. 1B
- Precautionary statements
- P264-P270-P280-P260-P273-P301+P312-P330-P302+P352-P312-P361+P364-P301+P330+P331-P303+P361+P353-P363-P304+P340-P310-P305+P351+P338-P391-P405-P501
- Hazardous Substances Data
- 1313-82-2(Hazardous Substances Data)
Chemistry & industry
Pharmacology
Mechanism of Action
The iv admin of Na2S at doses comparable to those absorbed during balneotherapy causes a significant reduction of bile flow in the anesthetized rat. The effect, different from that caused by acetylcholine, is completely inhibited and reverted by papaverine and not by atropine. Na2S possesses myotropic properties and the reduction of bile flow may be due to a spasmodic effect on the smooth muscle of biliary canaliculi.
Metabolism/Metabolites
NEITHER H2S2 NOR ANY VOLATILE SULFUR METABOLITES WERE FOUND IN EXPIRED BREATH OF MICE GIVEN SODIUM SULFIDE IP IN DOSES UP TO LD50. DETECTION SYSTEM WAS SENSITIVE TO LESS THAN 0.1% OF SULFUR IN GIVEN DOSES.
SODIUM...SOL SULFIDES ARE PROMPTLY & COMPLETELY HYDROLYZED IN BODY FLUIDS... /SULFIDE/
Heparinized rat blood containing sodium (35)S-sulfide was perfused through isolated rat lungs, kidney or liver. The rate and extent of sulfide oxidation varied from one organ to another. In the isolated perfused lung system, (35)S-sulfide was oxidized slowly to (35)S-thiosulfate; only small amounts of (35)S-sulfate were detectable, possibly due to the absence of sulfide oxidase. In the isolated perfused kidney system, (35)S-sulfide was oxidized to (35)S-sulfate with (35)S-thiosulfate as a possible intermediate. In liver perfusion expt, (35)S-sulfide was oxidized rapidly and almost exclusively to (35)S-sulfate. The addition of unlabeled thiosulfate inhibited the formation of (35)S-sulfate and caused the release of (35)S-thiosulfate from the isolated liver. Thiosulfate is an intermediate in sulfide oxidation to sulfate. A mechanism for the rapid oxidation of sulfide to thiosulfate was present in rat liver mitochondria and, in the presence of glutathione, the thiosulfate was oxiized to sulfate.
Absorption, Distribution and Excretion
ALKALI SULFIDES ARE RAPIDLY ABSORBED FROM INTESTINE. IT IS DOUBTFUL WHETHER SKIN ABSORBS ENOUGH TO CAUSE SYSTEMIC POISONING. /SULFIDES/
THE SULFIDE RADICAL IS IN PART EXCRETED BY LUNGS AND KIDNEYS AND AS METALLIC SULFIDES...BY THE BOWEL, AND IN PART OXIDIZED TO SULFATE AND THIOSULFATE AND EXCRETED BY THE KIDNEYS. /SULFIDES/
Uses & manufacturing
Uses
Used to make pulp and paper, to dehair hides, to treat ores (flotation agent), to precipitate metals from wastewater and sludge, to remove nitrogen oxides from gas streams, to polymerize styrene-butadiene, and to manufacture other chemical products; Used in engraving, lithography, cotton printing, and photography; [CHEMINFO]
Pulp and Paper Processing [Category: Industry]
Lithography printing [Category: Hobbies]
In prodn of heavy water for nuclear reactors
MEDICATION (VET)
In dehairing hides and wool pulling; desulfurizing viscose rayon; in the manufacture of rubber, sulfur dyes; in ore flotation, metal refining, engraving, cotton printing, as chemical intermediate, as laboratory reagent; in paper-pulping process.
U.S. Imports
(1972) NEGLIGIBLE
(1975) NEGLIGIBLE
Consumption Patterns
23% IS USED AS A DEPILATORY AGENT IN THE LEATHER INDUST; 21% AS AN INT FOR COLORS AND DYES; 16% AS AN INT FOR MISC CHEMS; 16% FOR THE PREPN OF RAYON AND CELLOPHANE FILM; 15% AS A FLOTATION AGENT IN ORE TREATMENT; AND 8% IN THE PREPN OF PULP AND PAPER (1968)
About 65% of 1990 U.S. sodium sulfide usage was in the leather industry for dehairing hides before tanning; 25% of 1990 U.S. sodium sulfide usage was in the production of miscellaneous chemicals.
Methods of Manufacturing
BY HEATING SODIUM ACID SULFATE WITH SALT & COAL TO ABOVE 950 °C, EXTRACTION WITH WATER, & CRYSTALLIZATION.
Sodium carbonate + barium sulfide (reaction); sodium sulfate + coal (reduction); sodium amalgam + sulfur (reaction); gasoline, catalytic-cracker (alkali extraction/acidification; coproduced with cresylic acid).
Best prepared from the elements in liquid ammonia, also obtained by dehydration of the nonahydrate: Courtois, Compt Rend 207, 1220 (1938); Klemm et al, Z Anorg Allgem Chem 241, 281 (1939); Feher in Handbook of Preparative Inorganic Chemistry, vol 1, G. Brauer, Ed. (Academic Press, New York, 2nd ed , 1963) pp 358-60.
Formulations/Preparations
GRADES: FLAKE; FUSED; CHIP SULFIDE (60% NA2S), 60% FUSED & BROKEN; 30% CRYSTALS; LIQUID.
Available commercially as fused, hydrated crystals containing 30-34% sodium sulfide or as flakes containing 60-62% sodium sulfide.
Applications
UsesIt can be used for the production of high-grade sulfur dye and high-quality leather. It can be used in the production of high-grade paper production in the paper industry. In the dye industry, it can be used for the production of sulfur dye and is the raw material of sulfur green and sulfur blue. In the printing and dyeing industry, it can be used as a facilitator agent for dissolving sulfur dye. In the tanning industry, it can be used for the hydrolysis for hair removal of raw skin and also used for the preparation of sodium polysulfide to help accelerate soaking and softening of dry skin. It can also be used as the cooking agent of papermaking industry. In fiber textile industry, it is used for the denitrofication of artificial fiber textile as well as the reduction of nitration as well as the mordant for cotton fabric dyeing. In the pharmaceutical industry, it is mainly used for the production of antipyretic drugs such as phenacetin. In addition, it can also be used for making sodium thiosulfate, sodium hydrosulfide, and sodium polysulfide. It can be used for analysis reagents and leather depilatory It can be used for the manufacture of dyes, sulfide, and used as ore flotation agent, depilatory rawhide, and the cooking agent of paper.
UsesThese yellow flakes were made by fusing sodium carbonate with sulfur. Soluble in water but less so in alcohol, sodium sulfide was lovingly called “stink” by those who used it for toning prints or intensifying negatives because of its sulfurous smell.
Usesused in sulfur dyes, used as reductant, mordant, floatation agent, depilatory for leather, digestion auxiliary in paper-making, and used in textile, pigment and rubber
UsesIt is used for H2S therapy, to study its effect on the prevention of diabetes in animals.
UsesSodium sulfide (Na2S) is used in the dye industry, in the oxidation process of gold, lead, and cooper metal ores, as a sheep dip, and to process paper.
General DescriptionSodium sulfide is a yellow to brick red crystalline mass or fused solid with an odor of rotten eggs. If exposed to moist air Sodium sulfide is liable to spontaneous heating and may cause ignition of nearby combustible material. Sodium sulfide absorbs moisture from the air.
Preparation methods
PreparationSodium sulfide is prepared by heating sodium bisulfate with sodium chloride and coal above 950°C. The product mixture is extracted with water and the hydrated sulfide is obtained from the solution by crystallization: NaHSO4 + NaCl + 2C → Na2S + 2CO2↑ + HCl↑Sodium sulfide also is produced from its elements in liquid ammonia: Na + 2S → Na2S.
Upstream & downstream products
Upstream raw materials
Downstream products
Suppliers50 total
Additional notes
DefinitionChEBI: A sulfide salt with formula Na2S. The pentahydrate and (particularly) the nonahydrate are also known. In gel form, sodium sulfide is used to soften toenails to assist in trimming (and so relive pain) of ingrowing toenails.
DefinitionA yellow-red solid, Na2S, formed by the reduction of sodium sulphate with carbon (coke) at elevated temperatures. It is a corrosive and readily oxidized material of variable composition and usually contains polysulphides of the type Na2S2, Na2S3, and Na2S4, which cause the variety of colours. It is known in an anhydrous form (r.d. 1.85; m.p. 1180°C) and as a nonahydrate, Na2S·9H2O (r.d. 1.43; decomposes at 920°C). Other hydrates of sodium sulphide have been reported. The compound is deliquescent, soluble in water with extensive hydrolysis, and slightly soluble in alcohol. It is used in wood pulping, dyestuffs manufacture, and metallurgy on account of its reducing properties. It has also been used for the production of sodium thiosulphate (for the photographic industry) and as a depilatory agent in leather preparation. It is a strong skin irritant.
Related reactions
Linked notes
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