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Home > Encyclopedia > Sulfamic acid, cobalt(2+) salt (2:1)

Sulfamic acid, cobalt(2+) salt (2:1)

Sulfamic acid, cobalt(2+) salt (2:1) structure

Sulfamic acid, cobalt(2+) salt (2:1) 

structure
  • CAS No:

    14017-41-5

  • Formula:

    Co.2H3NO3S

  • Chemical Name:

    Sulfamic acid, cobalt(2+) salt (2:1)

  • Synonyms:

    Sulfamic acid,cobalt(2+) salt (2:1);Cobalt sulfamate

  • Categories:

    Organic Chemistry  >  Amides

Description

COBALT (II) SULFAMATE is a reddish colored solid. COBALT (II) SULFAMATE is soluble in water. The primary hazard is the threat to the environment. Immediate steps should be taken to limit the spread to the environment. COBALT (II) SULFAMATE is used as a pigment and electroplating metals.


Cobaltous sulfamate is a reddish colored solid. It is soluble in water. The primary hazard is the threat to the environment. Immediate steps should be taken to limit the spread to the environment. It is used as a pigment and electroplating metals.|Liquid


Cobaltous sulfamate is a reddish colored solid. It is soluble in water. The primary hazard is the threat to the environment. Immediate steps should be taken to limit the spread to the environment. It is used as a pigment and electroplating metals.

Sulfamic acid, cobalt(2+) salt (2:1) Basic Attributes

251.1

250.884277

237-834-1

0UHD1PCY6U

9105

Reddish colored solid|Reddish crystalline solid

Characteristics

183

0.37280

Powder

soluble in water.

Odorless

Powder; Hygroscopic; Soluble in water /Cobalt(II) sulfamate hydrate/

Water soluble.

Salts, Basic

Salts, basic, such as COBALTOUS SULFAMATE, are generally soluble in water. The resulting solutions contain moderate concentrations of hydroxide ions and have pH's greater than 7.0. They react as bases to neutralize acids. These neutralizations generate heat, but less or far less than is generated by neutralization of the bases in reactivity group 10 (Bases) and the neutralization of amines. They usually do not react as either oxidizing agents or reducing agents but such behavior is not impossible. Contact with wood or paper may cause fire (USCG, 1999). Special Hazards of Combustion Products: Toxic oxides of nitrogen may form in fire.

Safety Information

II

6.1

UN 3261 8/PG 3

3

R34:Causes burns.

S23-S26-S36/37/39-S45

NX9110000

C

P201, P202, P261, P264, P270, P271, P272, P273, P280, P281, P285, P301+P312, P302+P352, P304+P340, P304+P341, P305+P351+P338, P308+P313, P312, P321, P330, P332+P313, P333+P313, P337+P313, P342+P311, P362, P363, P391, P403+P233, P405, P501

H302

SRP: 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 quality; potential migration in air, soil or water; effects on animal, aquatic and plant life; and conformance with environmental and public health regulations. If it is possible or reasonable use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination.

Special Hazards of Combustion Products: Toxic oxides of nitrogen may form in fire. Behavior in Fire: May increase the intensity of a fire. (USCG, 1999)

|Danger|H302 (89.36%): Harmful if swallowed [Warning Acute toxicity, oral]|P201, P202, P261, P264, P270, P271, P272, P273, P280, P281, P285, P301+P312, P302+P352, P304+P340, P304+P341, P305+P351+P338, P308+P313, P312, P321, P330, P332+P313, P333+P313, P337+P313, P342+P311, P362, P363, P391, P403+P233, P405, and P501|Aggregated GHS information provided by 47 companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.|H302: Harmful if swallowed [Warning Acute toxicity, oral]|P201, P202, P260, P261, P264, P270, P272, P280, P281, P285, P301+P312, P302+P352, P304+P341, P305+P351+P338, P308+P313, P314, P321, P330, P333+P313, P337+P313, P342+P311, P363, P405, and P501

Approved respirator, rubber gloves, safety goggles, protective clothing. (USCG, 1999)

If material involved in fire: Extinguish fire using agent suitable for type of surrounding fire. (Material itself does not burn or burns with difficulty.)

Environmental considerations: land spill: Dig a pit, pond, lagoon, holding area to contain liq or solid material /SRP: If time permits, pits, ponds, lagoons, soak holes, or holding areas should be sealed with an impermeable flexible membrane liner./ Cover solids with a plastic sheet to prevent dissolving in rain or fire fighting water.|Environmental considerations- water spill: Neutralize with agriculture lime (CaO), crushed limestone (CaCO3), or sodium bicarbonate (NaHCO3). Adjust pH to neutral (pH= 7). Use mechanical dredges or lifts to remove immobilized masses of pollutants and precipitates.|Liquid material spills can be copiously flushed with water and channeled to a treatment system or holding tank for reclamation or proper disposal. Spills of dry material can be removed by vacuuming or wet mopping. Some spills can be removed by hosing, first with a mist of water to dampen the spilled material and then with a more forceful stream that flushes it into a holding tank or other facility for handling contaminated water. Work surfaces or contaminated clothing should never be cleaned by dry sweeping or blowing with pressurized hoses. Recovery systems used to reclaim waste metals should comply with federal, state, and local regulations. All waste materials generated in the handling of cobalt-containing substances should be disposed of in compliance with federal, state, and local regulations. /Cobalt and cobalt salts/

If material not involved in fire: Keep material out of water sources and sewers. Build dike to contain flow as necessary.|Personnel protection: Keep upwind. ... Avoid breathing vapors or dusts. Wash away any material which may have contacted the body with copious amt of water or soap and water.|Employers should institute programs that emphasize good personal hygiene to prevent skin and respiratory irritation caused by cobalt containing dusts. After working with cobalt products, workers should thoroughly wash their hands and face before drinking, eating, or smoking. If skin contact with cobalt solutions occurs, the worker should wash the affected skin promptly. The employer should provide showers if workers have substantial contact with cobalt. These workers should be encouraged to wash or shower after each workshift. Employers should prohibit smoking or carrying of tobacco products, and should prohibit eating, food handling, or food storage within the work area. /Cobalt and cobalt salts/|General plant maintenance must be conducted regularly to prevent cobalt containing dusts from accumulating in work areas. Cleaning should be performed with vacuum pickup or wet mopping to minimize the amount of dust dispersed into the air. A decontamination room should be available for cleaning equipment that is to receive major overhaul or maintenance. Spills of cobalt-containing material should be promptly cleaned up to minimize inhalation or dermal contact. /Cobalt and cobalt salts/|Special precautions are necessary when workers must enter tanks or vessels, such as reaction vessels containing cobalt catalysts or vessels used to prepare cobalt salts. Before any worker enters a vessel, all sources for transferring cobalt and other materials into or out of the vessel must be blanked to prevent their entry. The vessel interior must then be washed with water and purged with air. After purging the vessel's atmosphere with suitable instruments to ensure that no hazards from fire, explosion, oxygen deficiency, or dust inhalation exist. No one should enter a tank or vessel without first being equipped with an appropriate respirator and a secured lifeline or harness. Mechanical ventilation should be provided continuously when workers are inside the tank. At least one other worker similarly equipped with respiratory protection, lifeline, and harness should watch at all times from outside the vessel. Workers inside the tank must be able to communicate with those persons outside. Other workers must be available to assist in an emergency. Flame- or spark-generating operations, such as welding or cutting, should be performed only when an authorized representative of the employer has signed a permit based on a finding that all necessary safety precautions have been taken. /Cobalt and cobalt salts/

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. Cobaltous sulfamate compounds are included on this list.

Persons in charge of vessels or facilities are required to notify the National Response Center (NRC) immediately, when there is a release of this designated hazardous substance, in an amount equal to or greater than its reportable quantity of 1000 lb or 454 kg. The toll free number of the NRC is (800) 424-8802. The rule for determining when notification is required is stated in 40 CFR 302.4 (section IV. D.3.b).

Toxicity

IDENTIFICATION AND USE: Cobaltous sulfamate is reddish crystalline solid. It is used as a pigment and for electroplating metals. HUMAN EXPOSURE AND TOXICITY: There are no data available. ANIMAL STUDIES: There are no data available.

Cobaltous sulfamate's production and use as a pigment, use in the electroplating of metals(1) and use in photonic device fabrication(2) may result in its release to the environment through various waste streams(SRC).

ATMOSPHERIC FATE: Inorganic cobalt compounds are nonvolatile and released into the atmosphere in particulate form(1). Particulate-phase cobalt compounds are removed from the air by wet and dry deposition(SRC). Cobalt has been detected in atmospheric deposition(2) and in rain-snow precipitation(3).

Food Chain Concentration Potential (cobaltous sulfamate hydrate): Bioconcentration of 200-1000 fold only under constant exposure. Not significant under spill conditions(1).

Occupational exposure to cobaltous sulfamate may occur through inhalation of dust and dermal contact with this compound at workplaces where cobaltous sulfamate is produced or used. (SRC)

Drug Information

Inhalation causes shortness of breath and coughing; permanent disability may occur. Ingestion causes pain and vomiting. Contact with eyes or skin causes irritation. (USCG, 1999)

INHALATION: Move to fresh air; if breathing has stopped, begin artificial respiration and call a doctor. INGESTION: Give large amount of water; induce vomiting; call a doctor. EYES: Flush with water for at least 15 minutes. SKIN: Flush with water. (USCG, 1999)

/SRP:/ Immediate First Aid: Ensure that adequate decontamination has been carried out as needed. If patient is not breathing, start artificial respiration, preferably with a demand valve resuscitator, bag-valve-mask device, or pocket mask, as trained. Perform CPR if necessary. Immediately flush contaminated eyes with gently flowing water. Do not induce vomiting. If vomiting occurs, lean patient forward or place on left side (Head-down position, if possible) to maintain an open airway and prevent aspiration. Keep patient quiet and maintain normal body temperature. Obtain medical attention. /Cobalt and Related Compounds/|/SRP:/ Basic treatment: Establish a patent airway (oropharyngeal or nasopharyngeal airway, if needed). Suction if necessary. Watch for signs of respiratory insufficiency and assist ventilations if needed. 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 ... . For eye contamination, flush eyes immediately with water. Irrigate each eye continuously with normal saline during transport ... . Do not use emetics. For ingestion, rinse mouth and administer 5 mL/kg up to 200 mL of water for dilution if the patient can swallow, has a strong gag reflex, and does not drool. Administer activated charcoal ... . /Cobalt and Related Compounds/|/SRP:/ Advanced treatment: Consider orotracheal or nasotracheal intubation for airway control in the patient who is unconscious, has severe pulmonary edema, or is in respiratory arrest. Positive pressure ventilation techniques with a bag valve mask device may be beneficial. Consider drug therapy for pulmonary edema ... . Consider administering a beta agonist such as albuterol for severe bronchospasm... . Monitor cardiac rhythm and treat arrhythmias as necessary ... . Start IV administration of D5W TKO (to keep open). Use 0.9% saline (NS) or lactated Ringer's if signs of hypovolemia are present. For hypotension with signs of hypovolemia, administer fluid cautiously. Watch for signs of fluid overload ... . Use proparacaine hydrochloride to assist eye irrigation ... . /Cobalt and Related Compounds/

Sulfamic acid, cobalt(2+) salt (2:1) Use and Manufacturing

Methods of Manufacturing

... Produced and sold as a solution containing about 10% cobalt. The product is formed by reaction of sulfamic acid and cobalt(II) carbonate or cobalt(II) hydroxide, or by the aeration of sulfamic acid slurries over cobalt metal.

Uses

Electroless plating, catalyst, electroplating, etc.


Plating agents and surface treating agents


Electrical and electronic products

Production

< 25,000 lb

Computer and electronic product manufacturing|Sulfamic acid, cobalt(2+) salt (2:1): ACTIVE

Computed Properties

Molecular Weight:251.11
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:8
Exact Mass:250.884272
Monoisotopic Mass:250.884272
Topological Polar Surface Area:183
Heavy Atom Count:11
Complexity:79.2
Covalently-Bonded Unit Count:3
Compound Is Canonicalized:Yes

Material

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