![]() |
Chemical Safety |
TOPIC |
PAGE |
| General Safety Guidelines | 13-2 |
| Hazard Communication Program | 13-7 |
| Corrosives | 13-9 |
| Flammables | 13-11 |
| Solvents | 13-15 |
| Toxic Chemicals | 13-17 |
| Reactives and Explosives | 13-22 |
| Cleaning Agents | 13-23 |
| Fume Hoods | 13-24 |
| Spill Response | 13-32 |
| Chemical Storage | 13-34 |
| Shipping/Receiving | 13-36 |
Almost everyone works with or around chemicals and
chemical products every day. Many
of these materials have properties that make them
hazardous: they can create physical (fire,
explosion) and/or health hazards (toxicity, chemical
burns). However, there are many ways
to work with chemicals which can both reduce the
probability of an accident to a negligible
level and reduce the consequences to minimum levels should
an accident occur. Risk
minimization depends on safe practices, appropriate
engineering controls for chemical
containment, the proper use of personnel protective
equipment, the use of the least quantity of
material necessary, and substitution of a less hazardous
chemical for the more hazardous one.
Before beginning an operation, ask "What would happen
if . . .?" The answer to this question
requires an understanding of the hazards associated with
the chemicals, equipment and
procedures involved. The hazardous properties of the
material and intended use will dictate
the precautions to be taken.
Another important distinction is the difference between
hazard and risk. The two terms are
sometimes used as synonyms. In fact, hazard is a much more
complex concept because it
includes conditions of use. The hazard presented by a
chemical has two components: (1) its
inherent capacity to do harm by virtue of its toxicity,
flammability, explosiveness,
corrosiveness, etc.; and (2) the ease with which the
chemical can come into contact with a
person or other object of concern. The two components
together determine risk (the
likelihood or probability that a chemical will cause harm).
Thus, an extremely toxic chemical
such as strychnine cannot cause poisoning if it is in a
sealed container and does not contact
the handler. In contrast, a chemical that is not highly
toxic can be lethal if a large amount is
ingested.
Chemical safety is inherently linked to
other safety issues including laboratory procedures,
personal protective equipment, electrical safety, fire
safety, and hazardous waste disposal.
Refer to other chapters in this manual for more information
on these topics. Knowledge + Common Sense + Caution = Chemical Safety
Not all chemicals are considered as hazardous.
Examples of nonhazardous chemicals
include buffers, sugars, starches, agar, and naturally
occurring amino acids.
The following sections provide general guidelines for
chemical safety.
Always follow these guidelines when working with chemicals:
The five prudent practices of chemical safety sum up these safety guidelines:
1. Treat all chemicals as if they were hazardous.
2. Minimize your exposure to any chemical.
3. Avoid repeated exposure to any chemical.
4. Never underestimate the potential hazard of any chemical or combination of chemicals.
5. Assume that a mixture or reaction product
is more hazardous than any component or
reactant.
Before using any chemical, read the container label and
the appropriate Material Safety Data
Sheets (MSDSs). Container labels and MSDSs are good sources
of information for
chemical safety. They provide the following information:
- Boiling point
- Vapor pressure
- Flammability
- Explosiveness
- Reactivity
- Toxic
- Carcinogens
- Irritants
Safe Handling Guidelines
Employees should treat all chemicals and equipment with caution and respect.
When working with chemicals, remember to do the following:
Likewise, when working with chemicals, remember the following:
Hygiene and Chemical Safety
Good personal hygiene will help minimize exposure to hazardous chemicals.
When working with chemicals, follow these guidelines:
In addition, follow these special precautions:
Hazard Communication Program
TAMU has a written program (TAMU Hazard Communication
Program) that complies with
OSHA standards and the Texas Hazard Communication Act for
hazardous chemicals. This
program is available from the Environmental Health &
Safety Department. It requires the
following:
Refer to the TAMU Hazard Communication Program and other
sections in this manual for
detailed information on these topics.
An integral part of hazard communication is hazard
identification. Everyone who works with
hazardous chemicals should know how to read and interpret
hazard information. Signs, like
the NFPA diamond in the illustration below, alert employees
to the known hazards in a
particular location.
The following is a detailed explanation of the NFPA hazard classification codes:
A corrosive chemical destroys or damages living tissue
by direct contact. Some acids, bases,
dehydrating agents, oxidizing agents, and organics are
corrosives.
Examples of Corrosives
Examples of acidic corrosives include the following:
Examples of alkaline corrosives include the following:
Examples of corrosive dehydrating agents include the following:
Examples of corrosive oxidizing agents include the following:
Examples of organic corrosives include the following:
NOTE:
Concentrated acids can cause painful burns that are
often superficial. Inorganic
hydroxides, however, can cause serious damage to skin
tissues because a protective
protein layer does not form. Even a dilute solution such
as sodium or potassium
hydroxide can saponify fat and attack skin. At first,
skin contact with phenol may not
be painful, but the exposed area may turn white due to
the severe burn. Systemic
poisoning may also result from dermal exposure.
Safe Handling Guidelines for Corrosives
To ensure safe handling of corrosives, the following
special handling procedures should be
used:
Corrosive Example: Perchloric Acid
Perchloric acid is a corrosive oxidizer that can be
dangerously reactive. At elevated
temperatures, it is a strong oxidizing agent and a strong
dehydrating reagent. Perchloric acid
reacts violently with organic materials. When combined with
combustible material, heated
perchloric acid may cause a fire or explosion. Cold
perchloric acid at less than 70%
concentration is not a very strong oxidizer, but its
oxidizing strength increases significantly at
concentrations higher than 70%. Anhydrous perchloric acid
(>85%) is very unstable and can
decompose spontaneously and violently.
If possible, purchase 60% perchloric acid instead of a
more concentrated grade. Always
wear gloves and goggles while using perchloric acid. Be
thoroughly familiar with the special
hazards associated with perchloric acid before using it.
Heated digestions with perchloric acid require a special
fume hood with a wash-down
system.
A flammable chemical is any solid, liquid, vapor, or gas
that ignites easily and burns rapidly in
air. Consult the appropriate MSDSs before beginning work
with flammables.
Flashpoint, Boiling Point, Ignition Temperature, and Class
Flammable chemicals are classified according to
flashpoint, boiling point, ignition
temperature. Flashpoint (FP) is the lowest temperature at
which a flammable liquid gives off
sufficient vapor to ignite. Boiling point (BP) is the
temperature at which the vapor pressure of
a liquid is equal to the atmospheric pressure under which
the liquid vaporizes. Flammable
liquids with low BPs generally present special fire
hazards. The FPs and BPs of certain
chemicals are closely linked to their ignition temperature
the lowest temperature at which a
chemical will ignite and burn independently of its heat
source.
The following table illustrates flammable class
characteristics:
| CLASS | FLASHPOINT (øF) |
BOILING POINT (øF) |
EXAMPLES |
||||||
1A |
<73 |
<100 |
Ethyl ether "Flammable" aerosols |
||||||
1B |
<73 |
ò100 |
Acetone Gasoline Toluene |
||||||
1C |
>73 |
<100 |
Butyl alcohol Methyl isobutyl ketone Turpentine |
||||||
2 |
100 - 140 |
--- |
Cyclohexane Kerosene Mineral spirits |
||||||
3A |
140 - 199 |
--- |
Butyl cellosolve |
| 3B | >200 | --- | Cellosolve Ethylene glycol Hexylene glycol |
The following table provides examples of common flammables and their flashpoint and
class.
CHEMICAL |
FLASHPOINT (øF) | CLASS |
| Acetone | 0 |
1B |
| Benzene | 12 |
1B |
| Butyl Acetate | >72 |
1C |
| Carbon Disulfide | -22 |
1B |
| Cyclohexane | -4 |
1B |
| Diethylene Glycol | 225 |
3B |
| Diethyl ether | -49 |
1A |
| Ethanol | 55 |
1B |
| Heptane | 25 |
1B |
| Isopropyl Alcohol | 53 |
1B |
| Methanol | 52 |
1B |
| Pentane | <-40 |
1A |
| Toluene | 40 |
1B |
Conditions for a Fire
Improper use of flammable liquids can cause a fire. The
following conditions must exist for a
fire to occur:
The following graphic illustrates the conditions for a fire:
When working with flammables, always take care to
minimize vapors which act as fuel.
Safe Handling Guidelines for Flammables
Follow these guidelines when working with flammable chemicals:
Organic solvents are often the most hazardous chemicals
in the work place. Solvents such as
ether, alcohols, and toluene, for example, are highly
volatile or flammable. Chlorinated
solvents such as chloroform are nonflammable, but when
exposed to heat or flame, may
produce carbon monoxide, chlorine, phosgene, or other
highly toxic gases.
Always use volatile and flammable solvents in an area
with good ventilation or in a fumehood.
Never use ether or other highly flammable solvents in a
room with open flames or other
ignition sources present.
Solvent Exposure Hazards
Health hazards associated with solvents include exposure by the following routes:
Inhalation of a solvent may
cause bronchial irritation, dizziness, central nervous system
depression, nausea, headache, coma, or
death. Prolonged exposure to excessive
concentrations of solvent vapors may
cause liver or kidney damage. The consumption of
alcoholic beverages can enhance these
effects.
Skin contact with solvents may lead to defatting, drying, and skin irritation.
Ingestion of a solvent may cause
severe toxicological effects. Seek medical attention
immediately.
The odor threshold for the following chemicals exceeds
acceptable exposure limits.
Therefore, if you can smell it, you may be overexposed
increase ventilation immediately.
NOTE:
Do not depend on your sense of smell alone to know when
hazardous vapors are
present. The odor of some chemicals is so strong that
they can be detected at levels far
below hazardous concentrations (e.g., xylene).
In addition, some solvents (e.g., benzene) are known or
suspected carcinogens.
Reducing Solvent Exposure
To decrease the effects of solvent exposure, substitute
hazardous solvents with less toxic or
hazardous solvents whenever possible. For example, use
hexane instead of diethyl ether,
benzene or a chlorinated solvent.
NOTE:
The best all-around
solvent is water; use it whenever possible.
The following table outlines possible solvent
substitutions:
| INSTEAD OF USING | SUBSTITUTE |
| Benzene | Cyclohexane Toluene Xylene |
|||||||
| Halogenated solvents | Nonhalogenated solvents | |||||||
| Aromatic hydrocarbon | Aliphatic hydrocarbon | |||||||
| Trichloroethylene | 1,1,1-trichloroethane | |||||||
| Diethyl ether | Hexane Petroleum ether |
Solvent Example:
DMSO
Dimethyl sulfoxide is unique because it is a good
solvent with many water-soluble as well as
lipid-soluble solutes. Due to these properties, dimethyl
sulfoxide is rapidly absorbed and
distributed throughout the body. It can also facilitate
absorption of other chemicals such as
grease, oils, cosmetics, and other chemicals that may
contact the skin.
The toxicity of a chemical refers to its ability to
damage an organ system (kidneys, liver),
disrupt a biochemical process (e.g., the blood-forming
process) or disturb an enzyme system
at some site remote from the site of contact. Toxicity is a
property of each chemical that is
determined by molecular structure. Any substance can be
harmful to living things. But, just as
there are degrees of being harmful, there are also degrees
of being safe. The biological
effects (beneficial, indifferent or toxic) of all chemicals
are dependent on a number of factors.
For every chemical, there are conditions in which it can
cause harm and, conversely, for
every chemical, there are conditions in which it does not.
A complex relationship exists
between a biologically active chemical and the effect it
produces that involves consideration
of dose (the amount of a substance to which one is
exposed), time (how often, and for how
long during a specific time, the exposure occurs), the
route of exposure (inhalation, ingestion,
absorption through skin or eyes), and many other factors
such as gender, reproductive
status, age, general health and nutrition, lifestyle
factors, previous sensitization, genetic
disposition, and exposure to other chemicals.
The most important factor is the dose-time relationship.
The dose-time relationship forms the
basis for distinguishing between two types of toxicity:
acute toxicity and chronic toxicity. The
acute toxicity of a chemical refers to its ability to
inflict systemic damage as a result (in most
cases) of a one-time exposure to relative large amounts of
the chemical. In most cases, the
exposure is sudden and results in an emergency situation.
Chronic toxicity refers to a chemical's ability to
inflict systemic damage as a result of repeated
exposures, over a prolonged time period, to relatively low
levels of the chemical. Some
chemicals are extremely toxic and are known primarily as
acute toxins (hydrogen cyanide);
some are known primarily as chronic toxins (lead). Other
chemicals, such as some of the
chlorinated solvents, can cause either acute or chronic
effects.
The toxic effects of chemicals can range from mild and
reversible (e.g. a headache from a
single episode of inhaling the vapors of petroleum naphtha
that disappears when the victim
gets fresh air) to serious and irreversible (liver or
kidney damage from excessive exposures
to chlorinated solvents). The toxic effects from chemical
exposure depend on the severity of
the exposures. Greater exposure and repeated exposure
generally lead to more severe
effects.
Exposure to toxic chemicals can occur by:
NOTE:
Inhalation and dermal absorption
are the most common methods of chemical
exposure in the workplace.
The following sections provide examples and safe
handling guidelines for the following types
of toxic chemicals:
IMPORTANT:
Minimize your exposure to any
toxic chemical.
Acute Toxins
Acute toxins can cause severe injury or death as a result of short-term, high-level exposure.
Examples of acute toxins include the following:
Do not work alone when handling acute toxins. Use a fume
hood to ensure proper
ventilation.
Chronic Toxins
Chronic toxins cause severe injury after repeated exposure.
Examples of chronic toxins include the following:
Carcinogens are materials that can cause cancer in
humans or animals. Several agencies
including OSHA, NIOSH, and IARC are responsible for
identifying carcinogens. There are
very few chemicals known to cause cancer in humans, but
there are many suspected
carcinogens and many substances with properties similar to
known carcinogens.
Examples of known carcinogens include the following:
Zero exposure should be the goal when working with known
or suspected carcinogens.
Workers who are routinely exposed to carcinogens should
undergo periodic medical
examinations.
Reproductive Toxins
Reproductive toxins are chemicals that can produce
adverse effects in parents and
developing embryos. Chemicals including heavy metals, some
aromatic solvents (benzene,
toluene, xylenes, etc.), and some therapeutic drugs are
capable of causing these effects. In
addition, the adverse reproductive potential of ionizing
radiation and certain lifestyle factors,
including excessive alcohol consumption, cigarette smoking,
and the use of illicit drugs, are
recognized.
While some factors are known to affect human
reproduction, knowledge in this field
(especially related to the male) is not as broadly
developed as other areas of toxicology. In
addition, the developing embryo is most vulnerable during
the time before the mother knows
she is pregnant. Therefore, it is prudent for all persons
with reproductive potential to minimize
chemical exposure.
Sensitizers
Sensitizers may cause little or no reaction upon first
exposure. Repeated exposures may
result in severe allergic reactions.
Examples of sensitizers include the following:
Irritants
Irritants cause reversible inflammation or irritation to
the eyes, respiratory tract, skin, and
mucous membranes. Irritants cause inflammation through
long-term exposure or high
concentration exposure. For the purpose of this section,
irritants do not include corrosives.
Examples of irritants include the following:
Reactive chemicals are sensitive to either friction or shock or they react in the presence of air, water, light, or heat. Explosive chemicals decompose or burn very rapidly when subjected to shock or ignition. Reactive and explosive chemicals produce large amounts of heat and gas; they are extremely dangerous.
Examples of reactive compounds include the following:
| REACTIVE CLASSIFICATION | CHEMICAL EXAMPLES |
| Acetylenic compounds | Acetylene Copper(I) acetylide |
| Azides | Benzenesulfonyl azide Lead (II) azide |
| Azo compounds | Azomethane Diazomethane |
| Chloro/perchloro compounds | Lead perchlorate Potassium chlorite Silver chlorate |
| Fulminates | Copper (II) fulminate Silver fulminate |
| Nitro compounds | Nitromethane Trinitrotoluene |
| Nitrogen-containing compounds | Silver amide Silver nitride |
| Organic peroxide formers | Diethyl ether Isopropyl ether |
| Picrates | Picric acid (dry) Lead picrate |
| Peroxides | Diacetyl peroxide Zinc peroxide |
| Strained ring compounds | Benzvalene Prismane |
| Polymerizable compounds | Butadiene Vinyl chloride |
Many of the chemicals contained in cleaning agents are
corrosive. Follow these guidelines
when working with any cleaning agent:
The following table outlines common cleaning agents, their hazards, and safety
precautions:
| CLEANING AGENT | POSSIBLE HAZARDS | SAFETY MEASURES |
| Ammonia | -Can cause severe eye and lung irritation. -If mixed with bleach, can form poisonous chlorine gas. |
-Use in a well ventilated area. -Do not mix with bleach. -Wear eye protection. |
| Bleach | -Can produce a poisonous gas if mixed with other cleaners. | -Never mix with toilet cleaners or ammonia. -Wear gloves and eye protection. |
| Toilet/Drain Cleaners & Lye | -Can cause serious burns. | -Wear gloves and avoid skin contact. -Never mix with bleach. -Protect eyes from possible splashes. |
| Cleaning Fluids/Degreasers | -May cause skin and eye irritations. -May contain solvents that can cause headaches, painful cough, dizziness, and liver or kidney damage. |
-Avoid direct contact. -Only use in well-ventilated areas. -Follow label directions carefully. |
| Aerosol Sprays | -Can irritate nasal passages if inhaled. -Can cause eye irritation. |
-Follow label directions carefully. -Use in well ventilated area. |
| Floor Waxes & Furniture Polish | -Can irritate skin and nasal passages. | -Use in well ventilated area. -Avoid skin contact. |
Fume hoods provide primary confinement in a chemical
laboratory. They exhaust toxic,
flammable, noxious, or hazardous fumes and vapors by
capturing, diluting, and removing
these materials. Fume hoods also provide physical
protection against fire, spills, and
explosion. Fume hoods provide the best protection when the
fume hood sash is in the closed
position. All chemical fume hoods must be ducted to the
outside of the building.
Types of Fume Hoods
There are three basic types of fume hoods: (1) standard,
(2) bypass, and (3) auxiliary air. In
addition, at TAMU, there are three classes of fume hoods:
A, B, and C.
STANDARD FUME HOODS
The face velocity of a standard fume hood is inversely
related to the open face area, allowing
a constant volume of air to be exhausted. If the sash is
lowered, the inflow air velocity
increases.
IMPORTANT:
Face velocity that is too high
may disturb sensitive apparatus, extinguish Bunsen
burners, or create excessive
turbulence.
BYPASS FUME HOODS
Bypass fume hoods are also called "balanced air"
or "constant volume" fume hoods. As the
sash is lowered, bypass fume hoods allow constant exhaust
volumes that help keep the room
ventilation system balanced. Constant exhaust volumes also
eliminate the problem of high
face velocity as the sash is lowered.
Bypass Fume Hood: Sash Open and Closed
AUXILIARY AIR FUME HOODS
Auxiliary air fume hoods are also known as "supplied
air" hoods. They use an outside air
supply for 50% to 70% of the hood's exhaust requirements.
This type of hood is designed to
reduce utility costs and conserve energy. The face velocity
of an auxiliary air fume hood may
vary.
Auxiliary Air Fume Hood: Sash Open and Closed
Classifications
CLASSIFICATION TYPES
The following guidelines are recommendations for face
velocities of three classes of chemical
fume hoods.
Recommended average face
velocity is 115 to 125 fpm with a minimum of 100 fpm at any
point. This class of hood is
suitable for use with highly toxic or volatile materials having a
TLV of less than 1 ppm (e.g.,
tetraethyl lead, beryllium compounds, metal carbonyls, and
carcinogens).
Recommended average face
velocity is 95 to 110 fpm with a minimum of 80 fpm at any
point. This class of hood is
suitable for use with materials having a TLV of 1-100 ppm
(e.g., acids, formaldehyde,
chloroform, and phenol).
Recommended average face
velocity is 75 to 95 fpm with a minimum of 60 fpm at any
point. This class of fume hood is
suitable for use with materials having a TLV greater than
100 ppm (e.g., ethanol, butanol,
and acetone). It is also suitable for operations that create
nuisance dust and fumes.
Special Fume Hoods
Special fume hoods are necessary when working with
certain chemicals and operations.
Examples of special fume hoods include the following:
These fume hoods have a water
spray system to wash down the entire length of the
exhaust duct, the baffle, and the
wall. The water spray is used periodically or after each use
to remove any perchloric acid or
organic material that may have accumulated.
These fume hoods have single
vertical sashes or double vertical sashes and an opening that
extends to the floor. These hoods
are typically used to accommodate large pieces of
equipment.
These hoods are labeled for use
with radioactive materials. The interior of these hoods is
resistant to decontamination
chemicals. If special filtration is necessary with these fume
hoods, contact the Environmental
Health & Safety Department.
These hoods capture upward
moving contaminants and are good for heat-producing
operations. Workers may be exposed
to contaminants if they work under the hood,
however.
Perchloric
Acid Fume Hood
Canopy Fume
Hood
Fume Hood Safety Considerations
The potential for glass breakage, spills, fires, and
explosions is great within a fume hood. Due
to the chance for fires or explosions, fume hoods should be
located towards the back of a
laboratory, away from primary and secondary exits. Practice
safe work habits when working
with fume hoods, including the following:
Employee traffic in front of a fume hoods or
opening/closing laboratory doors can interfere
with hood performance. Ensure that there is sufficient
aisle space in front of fume hoods.
All fume hoods are not appropriate for all types of
work. Ensure that hazardous chemicals
are used in the proper type or class of hood. For example,
use perchloric acid only in fume
hoods specifically designed for perchloric acid.
Fume Hood Use and Care
To ensure safety and proper fume hood performance, follow these guidelines:
IMPORTANT:
If a power failure or other
emergency occurs (e.g., building fire or fire within the
fume hood), close the fume hood
sash and call for emergency assistance.
Fume Hood Inspections
Fume hoods should be tested at least annually. Fume
hoods should also be tested in the
following circumstances:
The Environmental Health & Safety Department
performs fume hood inspections and testing.
The test includes an inspection of the hood system, airflow
measurements, and an assessment
of the use of the fume hood. If you suspect a problem with
your fume hood, please contact
the Environmental Health & Safety Department.
Spills are likely whenever chemicals are used. Personnel
should be trained and equipped to
handle most of the spills in their work area. The
Environmental Health & Safety
Department has a trained and equipped Chemical Spill
Response Team (CSRT). Contact
the Environmental Health & Safety Department for
assistance or advice about a chemical
spill.
Spill Prevention and Planning
Prevention is the best safety strategy for any
environment. Use safe handling procedures and
be aware of the potential hazards associated with
chemicals. For example, before working
with any chemicals, review the appropriate MSDSs.
Be prepared to respond to a chemical spill. To prepare
for a potential spill, follow these
guidelines:
Spill
Response Kit
Work areas that contain potentially hazardous chemicals
should have a chemical spill
response kit. This kit should include the following:
Responding to Chemical Spills
The following sequence provides a brief overview of proper chemical response procedures:
1. Notify others in the immediate area that a spill has
occurred. Evacuate the area if
necessary.
2. Attend to injured and exposed people.
3. Identify the spilled chemical(s).
4. Based on the hazards and the personal protective
equipment needed (e.g., respiratory
protection), determine if you can
safely clean the spill or if assistance is necessary. (Most
spills can be cleaned safely by the
people who were using the chemical.)
If you determine that you can safely clean the spill
without emergency assistance, follow these
guidelines:
Do not take unnecessary risks with chemical spills. Call
the Environmental Health & Safety
Department whenever a spill involves the following:
Proper chemical storage is as important to safety as
proper chemical handling. Often,
seemingly logical storage ideas, such as placing chemicals
in alphabetical order, may cause
incompatible chemicals to be stored together.
General Guidelines
Follow these guidelines for safe chemical storage:
Separating Hazardous Chemicals
In addition to the guidelines above, there are storage
requirements for separating hazardous
chemicals. Because an alphabetical storage system may place
incompatible chemicals next to
each other, group chemicals according to their hazard
category (i.e., acids, bases,
flammables, etc.).
Follow these guidelines to ensure that hazardous chemicals are stored safely:
The following table provides examples of incompatible
chemicals:
| CHEMICAL | INCOMPATIBLE WITH . . . |
| Acetic acid | Chromic acid, nitric acid, hydroxyl compounds, ethylene glycol, perchloric acid, peroxides, permanganates |
| Acetylene | Chlorine, bromine, copper, fluorine, silver, mercury |
| Acetone | Concentrated nitric and sulfuric acid mixtures |
| Alkali metals | Water, carbon tetrachloride or other chlorinated hydrocarbons, carbon dioxide, halogens |
| Ammonia | Mercury, chlorine, calcium hypochlorite, iodine, bromine, hydrofluoric acid |
| Chlorates | Ammonium salts, acids, powdered metals, sulfur, finely divided organic or combustible materials |
| Chlorine | Ammonia, acetylene, butadiene, butane, methane, propane (or other petroleum gases), hydrogen, sodium carbide, benzene, finely divided metals, turpentine |
| Cyanide | Acids |
| Fluorine | Most other chemicals |
| Nitrates | Sulfuric acid |
| Oxygen | Oils, grease, hydrogen, flammable liquids, solids, or gases |
| Perchloric acid | Acetic anhydride, bismuth and its alloys, alcohol, paper, wood, grease, oils, |
| Sodium | Carbon tetrachloride, carbon dioxide, water |
| Sulfides | Acids |
The U.S. Department of Transportation regulates the
shipment of hazardous materials.
Anyone who packages, receives, unpacks, signs for, or
transports hazardous chemicals must
be trained and certified in Hazardous Materials
Transportation. Warehouse personnel,
shipping and receiving clerks, truck drivers, and other
employees who pack or unpack
hazardous materials must receive this training. Contact the
Environmental Health & Safety
Department for more information on shipping or receiving
hazardous chemicals.