| Section 1. Identification | |||
|---|---|---|---|
| Chemical Name | Sodium borohydride | CAS No. | 16940-66-2 |
| Synonyms | sodium tetrahydrob-orate; sodiumborohydride | Chinese Name | 硼氢化钠 |
| Molecular Formula | NaBH | Molecular Weight | 37.833 |
| UN No. | 1426 | Data Source | PubChem (NIH/NLM) |
| GHS Hazard Classification | |
|---|---|
| Signal Word | DANGER |
| Pictograms | GHS02 · Flammable GHS05 · Corrosive GHS06 · Acute Toxic GHS07 · Irritant GHS08 · Health Hazard |
| Hazard Statements | H260H301H311H314H318H332H360H335 |
| Precautionary Statements | P203P223P231+P232P260P261P262P264P264+P265P270P271P280P301+P316P301+P330+P331P302+P335+P334P302+P352P302+P361+P354P304+P340P305+P354+P338P316P317P318P321P330P361+P364P363P370+P378P402+P404P405P501P319P403+P233 |
| Contents | |||
|---|---|---|---|
| Section 2 | Hazards Identification | Section 4 | First-Aid Measures |
| Section 5 | Fire-Fighting Measures | Section 6 | Accidental Release Measures |
| Section 7 | Handling and Storage | Section 8 | Exposure Controls / Personal Protection |
| Section 9 | Physical and Chemical Properties | Section 10 | Stability and Reactivity |
| Section 11 | Toxicological Information | Section 12 | Ecological Information |
| Section 13 | Disposal Considerations | Section 14 | Transport Information |
This chemical does not meet GHS hazard criteria for 0.4% (3 of 671) of reports.
H260 (86.7%): In contact with water releases flammable gases which may ignite spontaneously [Danger Substances and mixtures which in contact with water, emit flammable gases]
H301 (99.6%): Toxic if swallowed [Danger Acute toxicity, oral]
H311 (23%): Toxic in contact with skin [Danger Acute toxicity, dermal]
H314 (99.6%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
H318 (71.4%): Causes serious eye damage [Danger Serious eye damage/eye irritation]
H332 (16.7%): Harmful if inhaled [Warning Acute toxicity, inhalation]
H360 (43.7%): May damage fertility or the unborn child [Danger Reproductive toxicity]
P203, P223, P231+P232, P260, P261, P262, P264, P264+P265, P270, P271, P280, P301+P316, P301+P330+P331, P302+P335+P334, P302+P352, P302+P361+P354, P304+P340, P305+P354+P338, P316, P317, P318, P321, P330, P361+P364, P363, P370+P378, P402+P404, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 671 reports by companies from 41 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Reported as not meeting GHS hazard criteria per 3 of 671 reports by companies.
There are 40 notifications provided by 668 of 671 reports by companies with hazard statement code(s).
Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.
H260: In contact with water releases flammable gases which may ignite spontaneously [Danger Substances and mixtures which in contact with water, emit flammable gases]
H301: Toxic if swallowed [Danger Acute toxicity, oral]
H314: Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
H318: Causes serious eye damage [Danger Serious eye damage/eye irritation]
H335: May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]
P223, P231+P232, P260, P261, P264, P264+P265, P270, P271, P280, P301+P316, P301+P330+P331, P302+P335+P334, P302+P361+P354, P304+P340, P305+P354+P338, P316, P317, P319, P321, P330, P363, P370+P378, P402+P404, P403+P233, P405, and P501 (click each P-code to see the statement)
Fresh air, rest. Refer immediately 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 .
Rinse with plenty of water for several minutes (remove contact lenses if easily possible). Refer immediately for medical attention.
Rinse mouth. Give one or two glasses of water to drink. Do NOT induce vomiting. Refer immediately for medical attention.
INGESTION: do NOT induce vomiting; give dilute vinegar, lemon juice, milk, or olive oil; call a doctor.
SKIN AND EYES: flood with large amount of water. (USCG, 1999)
General First Aid:
· Call 911 or emergency medical service.
· Ensure that medical personnel are aware of the material(s) involved, take precautions to protect themselves and avoid contamination.
· Move victim to fresh air if it can be done safely.
· Administer oxygen if breathing is difficult.
· If victim is not breathing:
-- DO NOT perform mouth-to-mouth resuscitation; the victim may have ingested or inhaled the substance.
-- If equipped and pulse detected, wash face and mouth, then give artificial respiration using a proper respiratory medical device (bag-valve mask, pocket mask equipped with a one-way valve or other device).
-- If no pulse detected or no respiratory medical device available, provide continuous compressions. Conduct a pulse check every two minutes or monitor for any signs of spontaneous respirations.
· Remove and isolate contaminated clothing and shoes.
· For minor skin contact, avoid spreading material on unaffected skin.
· In case of contact with substance, remove immediately by flushing skin or eyes with running water for at least 20 minutes.
· For severe burns, immediate medical attention is required.
· Effects of exposure (inhalation, ingestion, or skin contact) to substance may be delayed.
· Keep victim calm and warm.
· Keep victim under observation.
· For further assistance, contact your local Poison Control Center.
· Note: Basic Life Support (BLS) and Advanced Life Support (ALS) should be done by trained professionals.
Specific First Aid:
· In case of contact with substance, wipe from skin immediately; flush skin or eyes with running water for at least 20 minutes.
In Canada, an Emergency Response Assistance Plan (ERAP) may be required for this product. Please consult the shipping paper and/or the "ERAP" section.
Excerpt from ERG Guide 138 [Substances - Water-Reactive (Emitting Flammable Gases)]:
DO NOT USE WATER OR FOAM.
SMALL FIRE: Dry chemical, soda ash, lime or sand.
LARGE FIRE: DRY sand, dry chemical, soda ash or lime or withdraw from area and let fire burn. If it can be done safely, move undamaged containers away from the area around the fire.
FIRE INVOLVING METALS OR POWDERS (ALUMINUM, LITHIUM, MAGNESIUM, ETC.): Use dry chemical, DRY sand, sodium chloride powder, graphite powder or class D extinguishers; in addition, for Lithium you may use Lith-X® powder or copper powder. Also, see ERG Guide 170.
FIRE INVOLVING TANKS, RAIL TANK CARS OR HIGHWAY TANKS: Fight fire from maximum distance or use unmanned master stream devices 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 in direct contact with flames. (ERG, 2024)
Use dry sand, dry powder. NO water. NO foam. NO carbon dioxide.
Fire extinguishing agents: graphite, limestone, soda ash, sodium chloride powders
Fire extinguishing agents not to be used: Water, carbon dioxide, or halogenated extinguishing agents.
If material on fire or involved in fire: Do not use water. Use graphite, soda ash, powdered sodium chloride, or suitable dry powder.
· 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.
· Keep unauthorized personnel away.
· Stay upwind, uphill and/or upstream.
· Ventilate closed spaces before entering, but only if properly trained and equipped.
· ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.
· Do not touch or walk through spilled material.
· Stop leak if you can do it without risk.
· Use water spray to reduce vapors or divert vapor cloud drift. Avoid allowing water runoff to contact spilled material.
· DO NOT GET WATER on spilled substance or inside containers.
Small Spill
· Cover with DRY earth, DRY sand or other non-combustible material followed with plastic sheet to minimize spreading or contact with rain.
· Dike for later disposal; do not apply water unless directed to do so.
Powder Spill
· Cover powder spill with plastic sheet or tarp to minimize spreading and keep powder dry.
· DO NOT CLEAN-UP OR DISPOSE OF, EXCEPT UNDER SUPERVISION OF A SPECIALIST.
Excerpt from ERG Guide 138 [Substances - Water-Reactive (Emitting Flammable Gases)]:
IMMEDIATE PRECAUTIONARY MEASURE: Isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids.
LARGE SPILL: Consider initial downwind evacuation for at least 300 meters (1000 feet).
FIRE: If tank, rail tank car or highway tank 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. (ERG, 2024)
Immediate precautionary measure
· Isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids.
Large Spill
· Consider initial downwind evacuation for at least 300 meters (1000 feet).
· If tank, rail tank car or highway tank 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.
Remove all ignition sources. Personal protection: chemical protection suit and particulate filter respirator adapted to the airborne concentration of the substance. Sweep spilled substance into covered dry, plastic containers. Carefully collect remainder. Then store and dispose of according to local regulations.
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 quality; potential migration in soil or water; effects on animal, aquatic, and plant life; and conformance with environmental and public health regulations.
Obvious industrial hygiene recommendations /include/ (1) sodium borohydride is flammable and exothermic in presence of moisture and should be handled with special care to prevent serious burns, and (2) measures should be taken to prevent workers from ocular, cutaneous, or inhalation exposures ...
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. Contaminated clothing should not be taken home at end of shift, but should remain at employee's place of work for cleaning.
SRP: The scientific literature for the use of contact lenses in industry is conflicting. The benefit or detrimental effects of wearing contact lenses depend not only upon the substance, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses. However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye. In those specific cases, contact lenses should not be worn. In any event, the usual eye protection equipment should be worn even when contact lenses are in place.
If material not on fire and not involved in fire: Do not use water. Keep sparks, flames, and other sources of ignition away. Keep out of water sources and sewers. Keep material dry. Do not attempt to sweep up dry material.
For more Preventive Measures (Complete) data for SODIUM BOROHYDRIDE (8 total), please visit the HSDB record page.
Excerpt from ERG Guide 138 [Substances - Water-Reactive (Emitting Flammable Gases)]:
ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area. Do not touch or walk through spilled material. Stop leak if you can do it without risk. Use water spray to reduce vapors or divert vapor cloud drift. Avoid allowing water runoff to contact spilled material. DO NOT GET WATER on spilled substance or inside containers.
SMALL SPILL: Cover with DRY earth, DRY sand or other non-combustible material followed with plastic sheet to minimize spreading or contact with rain. Dike for later disposal; do not apply water unless directed to do so.
POWDER SPILL: Cover powder spill with plastic sheet or tarp to minimize spreading and keep powder dry. DO NOT CLEAN-UP OR DISPOSE OF, EXCEPT UNDER SUPERVISION OF A SPECIALIST. (ERG, 2024)
Dry. Well closed. Separated from strong acids, alcohols, powdered metals and water.
Storage temperature: ambient. Venting: sealed containers must be stored in well-ventilated area.
· Wear positive pressure self-contained breathing apparatus (SCBA).
· Wear chemical protective clothing that is specifically recommended by the manufacturer when there is NO RISK OF FIRE.
· Structural firefighters' protective clothing provides thermal protection but only limited chemical protection.
0.48 [mg/m3]
5.3 [mg/m3]
32 [mg/m3]
· DO NOT USE WATER OR FOAM.
Small Fire
· Dry chemical, soda ash, lime or sand.
Large Fire
· DRY sand, dry chemical, soda ash or lime or withdraw from area and let fire burn.
· If it can be done safely, move undamaged containers away from the area around the fire.
Fire Involving Metals or Powders (Aluminum, Lithium, Magnesium, etc.)
· Use dry chemical, DRY sand, sodium chloride powder, graphite powder or class D extinguishers; in addition, for Lithium you may use Lith-X® powder or copper powder. Also, see GUIDE 170.
Fire Involving Tanks, Rail Tank Cars or Highway Tanks
· Fight fire from maximum distance or use unmanned master stream devices 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 in direct contact with flames.
1-5 mg/cu m (USSR) /Borates/
Limit for livestock is 5 ug/mL boron in water. /Boron/
0.5 mg/L maximum (USSR) /Boron in drinking water/
A harmful concentration of airborne particles can be reached quickly when dispersed.
The substance is corrosive to the eyes, skin and respiratory tract. Corrosive on ingestion.
Goggles, rubber gloves, and protective clothing. (USCG, 1999)
/Wear/ goggles, rubber gloves, and protective clothing
/Due to the/ extremely hazardous nature of boron hydrides, the use of personal protective equipment /should be considered/ even where max engineering safety measures are applied. Workers should be supplied with resp protective equipment ... of canister-supplied air type ... or self-contained type depending on ... concn. Eye and face protection, impervious overalls, hand, arm, foot and leg protection should ... be worn. /Boranes/
NO open flames.
AVOID ALL CONTACT! IN ALL CASES CONSULT A DOCTOR!
Use local exhaust or breathing protection.
Protective gloves. Protective clothing.
Wear safety goggles or eye protection in combination with breathing protection.
Do not eat, drink, or smoke during work.
Sodium borohydride is a white to grayish crystalline powder. It is decomposed by water to form sodium hydroxide, a corrosive material, and hydrogen, a flammable gas. The heat of this reaction may be sufficient to ignite the hydrogen. The material itself is easily ignited and burns vigorously once ignited. It is used to make other chemicals, treat waste water, and for many other uses.
Dry Powder; Liquid; Dry Powder
Gray to white crystals or powder; [HSDB]
WHITE CRYSTALLINE POWDER.
White to gray-white microcystalline powder or lumps
White cubic crystals, hygroscopic
>400 °C (vacuum) (decomposes)
Soluble in "Cellosolve" ether
Soluble in ammonia, amines, pyridine, dimethyl ether of diethylene glycol; insoluble in other ethers, hydrocarbons, alkyl chlorides
Solubility (wt/wt) in liquid ammonia, 104% at 25 °C; in ethylenediamine, 22% at 75 °C; in morpholine, 1.4% at 25 °C; in pyridine, 3.1% at 25 °C; in methanol, 16.4% at 20 °C (reacts); in ethanol, 4.0% at 20 °C (reacts slowly); in tetrahydrofuran, 0.1% at 20 °C; in diglyime, 5.5% at 20 °C; in dimethylformamide, 18.0% at 20 °C
Solubility (wt/wt) in water: 55% at 25 °C; 88.5% at 60 °C
Solubility in water, g/100ml at 25 °C: 55
1.074 at 68 °F (USCG, 1999) - Denser than water; will sink
1.074 g/cu cm (anhydrous material)
1.07 g/cm³
1.07 @25 °C
Anhydrous material is stable in dry air to 300 °C; decomposes slowly at 400 °C and rapidly at 500 °C
Aqueous solutions are most stable in the presence of small amounts of sodium hydroxide (0.2% for a nearly saturated solution containing 44% sodium borohydride) and can be kept for several days.
When heated to decomposition emits toxic fumes of /sodium oxides/.
Solutions are rapidly decomposed by boiling.
INDEX OF REFRACTION: 1.542
Hygroscopic, cubic crystals forming a dihydrate, mp 36-37 °C; anhydrous material is stable in dry air to 300 °C; decomposes slowly at 400 °C and rapidly at 500 °C
Aqueous solutions are most stable in the presence of small amounts of NaOH (0.2% for a nearly saturated solution containing 44% NaBH4) and can be kept for several days; solutions are rapidly decomposed by boiling
Standard enthalpy of formation: -188.6 kJ/mol (crystal); Molar heat capacity 86.8 J/mol K at 25 °C (crystal)
Decomposes on heating to constituent elements
Metals -> Metal Hydrides
Reactive agents - 1st degree
FLAVORING AGENT OR ADJUVANT -> FDA Substance added to food
Hydrolysis generates enough heat to ignite adjacent combustible material [Haz. Chem. Data 1966]. Dissolves in water with liberation of heat, may steam and spatter. Solution is basic (alkaline). Reaction of water with the borohydride liberates flammable hydrogen gas. Sodium borohydride burns in air [Lab. Gov. Chemist 1965].
Metal Hydrides, Metal Alkyls, Metal Aryls, and Silanes
Strong Reducing Agent
Water-Reactive
Air-Reactive
CSL00015
SODIUM BOROHYDRIDE + TRIFLUOROACETIC ACID
Warning - Sodium Borohydride combined with Trifluoroacetic acid can result in a fire
Flammable,Pyrophoric
User-Reported
CSL00038
SODIUM BOROHYDRIDE + WATER
Gas evolution. Ensure complete destruction of borane by using appropriate quench time and pH
Gas Under Pressure
borohydride
CSL00087
SODIUM BOROHYDRIDE + LITHIUM BOROHYDRIDE
A small amount of residual lithium borohydride was cleaned up with bleach and paper towels, which were placed in a trash can. The trash can subsequently caught fire.
Pyrophoric,Water Reactive
Preventive action -Dispose weighing material that came in contact with borohydride into a dry container and dispose of as waste -Substitute ethanol for bleach when wiping equipment and bench tops
CSL00159
Sodium borohydride + Ethanol
Reaction resulted in a fire.
Not Available
Substance identification sources: Sodium borohydride. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=16940-66-2 (retrieved 2022-01-27) (CAS RN: 16940-66-2). Ethanol. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=64-17-5 (retrieved 2022-01-27) (CAS RN: 64-17-5).
User Reported
01/27/2022
SODIUM BOROHYDRIDE is a powerful reducing agent. A chemical base. Absorbs moisture readily forming caustic solution. which attacks aluminum and zinc. A violent polymerization of acetaldehyde results from the reactions of acetaldehyde with alkaline materials such as sodium hydroxide. Calcium oxide or sodium hydroxide react with phosphorus pentaoxide extremely violently when initiated by local heating [Mellor 8 Supp.3:406 (1971]. Using potassium hydroxide to dry impure tetrahydrofuran, which contains peroxides, may be hazardous. Explosions have occurred in the past. Sodium hydroxide behaves in a similar way as potassium hydroxide [NSC Newsletter, Chem. Soc. 1967]. Ignition occurs if a mixture of the hydride and sulfuric acid is not cooled. Contact of glycerol and sodium borohydride leads to ignition, other glycols and methanol are exothermic but do not ignite.
Reacts with water or steam to produce hydrogen.
... On contact with acid fumes, it can emit flammable vapors.
Dry mixtures with sodium hydroxide containing 15-40% of /sodium/ tetrahydroborate liberate hydrogen explosively at 230-270 °C.
Addition of a 4% solution of sodium tetrahydroborate in diglyme containing 0.09% of water to a 27% solution of aluminium chloride in the same solvent led to a violent explosion, attributed to formation and ignition of hydrogen.
For more Hazardous Reactivities and Incompatibilities (Complete) data for SODIUM BOROHYDRIDE (19 total), please visit the HSDB record page.
Serious local effects by all routes of exposure.
Burning sensation. Cough. Sore throat. Laboured breathing. Shortness of breath.
Redness. Pain. Skin burns.
Redness. Pain. Severe deep burns.
Burning sensation in the throat and chest. Abdominal pain. Vomiting. Shock or collapse.
Neurotoxin - Other CNS neurotoxin
Dermatotoxin - Skin burns.
Toxic Pneumonitis - Inflammation of the lungs induced by inhalation of metal fumes or toxic gases and vapors.
LC50 (rat) = 36 mg/m3
LD50 Rat oral 160 mg/kg bw
LD50 Rat ip 18 mg/kg
Maintain an open airway and assist ventilation if nescessary. treat coma, seizures, hypotension, and renal failure if they occur. There is no specific antidote. Administer activated charcoal (although boric acid is not well absorbed). Consider gastric lavage for large ingestions. /Boric acid, Borates, and Boron/
Hemodialysis is effective and is indicated after massive ingestions and for supportive care of renal failure. Peritoneal dialysishas not proved effective in enhancing elimination in infants. /Boric acid, Borates, and Boron/
In acute poisonings, if a large amount has been ingested and the patient is seen within one hour of exposure, gastrointestinal decontamination should be considered ... .It is important to keep in mind that vomiting and diarrhea are common, and severe poisoning may be associated with seizures. Therefore induction of emesis by syrup of ipecac is probably contraindicated in these exposures. Catharsis is not indicated if diarrhea is present. /Boric acid and Borates/
If ingestion of borate has been massive (several grams), or has extended over several days, administer intravenous glucose and electrolyte solutions to sustain urinary excretion of borate. Monitor fluid balance and serum electrolytes (including bicarbonate capacity ) regularly. Monitor cardiac status by ECG. Test the urine for proteins and cells to detect renal injury, and monitor serum concentration of borate. Metabolic acidosis may be treated with sodium bicarbonate. If shock develops, it may be necessary to infuse plasma or whole blood. Administer oxygen continuously. If oliguria (less than 25 to 30 mL urine per hour) occurs, intravenous fluids must be slowed or stopped to avoid overloading the circulation. Such patients should be referred to a center capable of providing intensive care for critically ill patients. /Boric acid and Borates/
For more Antidote and Emergency Treatment (Complete) data for SODIUM BOROHYDRIDE (7 total), please visit the HSDB record page.
No specific considerations are needed for boric acid or borates except for general health and liver and kidney function. /Boric acid and borates/
/LABORATORY ANIMALS: Acute Exposure/ By dermal application to the moist back of rabbits 6 of 10 died when 400 mg was applied in 2 doses in the same area; however, when the same application was made in different areas, no deaths resulted. ... Sodium borohydride on dry skin ... produced no signs of irritation.
/LABORATORY ANIMALS: Acute Exposure/ When instilled into the eye of rabbits, 1 mg sodium borohydride produced irreversible damage ...
Inorganic boron compounds (with the exception of hydroboranes) are expected to be nonvolatile and will exist solely in the particulate phase in the ambient atmosphere. Particulate-phase boron compounds will be removed from the atmosphere by wet and dry deposition. The chemistry of boron is dominated by its tendency to form stable bonds with electronegative atoms, especially oxygen. Reduced boron compounds (halides, hydrides, alkyls and aryls) tend to oxidize and hydrolyze readily, and would be expected to be converted into various boron-oxide compounds in the environment. Inorganic boron compounds are nonvolatile and would not be expected to volatilize from moist or dry soil surfaces. Since the adsorption of boron is expected to be most significant for soils that contain high concentrations of amorphous aluminum and iron oxides and hydroxides, sediments with these characteristics may also strongly adsorb boron compounds. (SRC)
Inorganic boron compounds (with the exception of hydroboranes) are expected to be nonvolatile and will exist solely in the particulate phase in the ambient atmosphere. Particulate-phase boron compounds will be removed from the atmosphere by wet and dry deposition. The chemistry of boron is dominated by its tendency to form stable bonds with electronegative atoms, especially oxygen. Reduced boron compounds (halides, hydrides, alkyls and aryls) tend to oxidize and hydrolyze readily, and would be expected to be converted into various boron-oxide compounds in the environment. Inorganic boron compounds are nonvolatile and would not be expected to volatilize from moist or dry soil surfaces. Since the adsorption of boron is expected to be most significant for soils that contain high concentrations of amorphous aluminum and iron oxides and hydroxides, sediments with these characteristics may also strongly adsorb boron compounds. (SRC)
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 quality; potential migration in soil or water; effects on animal, aquatic, and plant life; and conformance with environmental and public health regulations.
/GUIDE 138: SUBSTANCES - WATER-REACTIVE (Emitting Flammable Gases)/ Fire or Explosion: Produce flammable gases on contact with water. May ignite on contact with water or moist air. Some react vigorously or explosively on contact with water. May be ignited by heat, sparks or flames. May re-ignite after fire is extinguished. Some are transported in highly flammable liquids. Runoff may create fire or explosion hazard.
/GUIDE 138: SUBSTANCES - WATER-REACTIVE (Emitting Flammable Gases)/ Health: Inhalation or contact with vapors, substance or decomposition products may cause severe injury or death. May produce corrosive solutions on contact with water. Fire will produce irritating, corrosive and/or toxic gases. Runoff from fire control may cause pollution.
/GUIDE 138: SUBSTANCES - WATER-REACTIVE (Emitting Flammable Gases)/ Public Safety: CALL Emergency Response Telephone Number on Shipping Paper first. If Shipping Paper not available or no answer, refer to appropriate telephone number listed on the inside back cover. As an immediate precautionary measure, isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids. Keep unauthorized personnel away. Stay upwind. Keep out of low areas. Ventilate the area before entry.
/GUIDE 138: SUBSTANCES - WATER-REACTIVE (Emitting Flammable Gases)/ Protective Clothing: Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective clothing that is specifically recommended by the manufacturer. It may provide little or no thermal protection. Structural firefighters' protective clothing provides limited protection in fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible.
For more DOT Emergency Guidelines (Complete) data for SODIUM BOROHYDRIDE (8 total), please visit the HSDB record page.
UN 1426; Sodium borohydride
IMO 4.3; Sodium borohydride
No person may /transport,/ offer or accept a hazardous material for transportation in commerce unless that person is registered in conformance ... and the hazardous material is properly classed, described, packaged, marked, labeled, and in condition for shipment as required or authorized by ... /the hazardous materials regulations (49 CFR 171-177)./
The International Air Transport Association (IATA) Dangerous Goods Regulations are published by the IATA Dangerous Goods Board pursuant to IATA Resolutions 618 and 619 and constitute a manual of industry carrier regulations to be followed by all IATA Member airlines when transporting hazardous materials.
The International Maritime Dangerous Goods Code lays down basic principles for transporting hazardous chemicals. Detailed recommendations for individual substances and a number of recommendations for good practice are included in the classes dealing with such substances. A general index of technical names has also been compiled. This index should always be consulted when attempting to locate the appropriate procedures to be used when shipping any substance or article.
Dangerous When Wet
UN Hazard Class: 4.3; UN Pack Group: I