UNICOOL R-404A Safety Data Sheet
UNICOOL R-404A Safety Data Sheet
SECTION 1 Identification
Product Identifier
Product name UNICOOL R-404A
Name, address, and telephone number of the chemical manufacturer, importer, or other responsible party
Outback (M)SDS portal:
Wilhelmsen Ships Service AS*
Registered company name Wilhelmsen Ships Service [Link]
Central Warehouse
login=wilhelmsen
--------Use our Outback portal to obtain our (M)SDSs
9400 New Century Drive in other languages and/or format.--------- For
Willem Barentszstraat 50
Address Pasadena, TX 77507 United questions relating to our SDSs please use Email:
Rotterdam Netherlands
States [Link]@[Link] ---------
Norway
Telephone +1 281 867 2000 +31 10 4877 777 Not Available
Emergency telephone
+31-10-4877700 + 31 88 7558561 +31-10-4877700
numbers
Other emergency
+31-10-4877700 + 31 10 4877700 +31-10-4877700
telephone numbers
Emergency telephone
+1 855-237-5573
numbers
Other emergency
+61 3 9573 3188
telephone numbers
Once connected and if the message is not in your preferred language then please dial 01
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UNICOOL R-404A
Una vez conectado y si el mensaje no está en su idioma preferido, por favor marque 02
Classification Gases Under Pressure (Liquefied Gas), Skin Corrosion/Irritation Category 2, Simple Asphyxiant
Label elements
Hazard pictogram(s)
Hazard statement(s)
H280 Contains gas under pressure; may explode if heated.
H315 Causes skin irritation.
Substances
See section below for composition of Mixtures
Mixtures
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UNICOOL R-404A
354-33-6 44 pentafluoroethane
811-97-2 4 1,1,1,2-tetrafluoroethane
420-46-2 52 1,1,1-trifluoroethane
Inhalation; remove victim from exposure, and give supplemental oxygen if available.
Ingestion; (a) Prehospital: Administer activated charcoal, if available. DO NOT induce vomiting because of rapid absorption and the risk of abrupt onset CNS
depression. (b) Hospital: Administer activated charcoal, although the efficacy of charcoal is unknown. Perform gastric lavage only if the ingestion was very
large and recent (less than 30 minutes)
D: Enhanced elimination:
There is no documented efficacy for diuresis, haemodialysis, haemoperfusion, or repeat-dose charcoal.
POISONING and DRUG OVERDOSE, Californian Poison Control System Ed. Kent R Olson; 3rd Edition
Do not administer sympathomimetic drugs unless absolutely necessary as material may increase myocardial irritability.
No specific antidote.
Because rapid absorption may occur through lungs if aspirated and cause systematic effects, the decision of whether to induce vomiting or not should be
made by an attending physician.
If lavage is performed, suggest endotracheal and/or esophageal control.
Danger from lung aspiration must be weighed against toxicity when considering emptying the stomach.
Treatment based on judgment of the physician in response to reactions of the patient
For frost-bite caused by liquefied petroleum gas:
If part has not thawed, place in warm water bath (41-46 C) for 15-20 minutes, until the skin turns pink or red.
Analgesia may be necessary while thawing.
If there has been a massive exposure, the general body temperature must be depressed, and the patient must be immediately rewarmed by whole-body
immersion, in a bath at the above temperature.
Shock may occur during rewarming.
Administer tetanus toxoid booster after hospitalization.
Prophylactic antibiotics may be useful.
The patient may require anticoagulants and oxygen.
[Shell Australia 22/12/87]
For gas exposures:
--------------------------------------------------------------
BASIC TREATMENT
--------------------------------------------------------------
Establish a patent airway with suction where necessary.
Watch for signs of respiratory insufficiency and assist ventilation as necessary.
Administer oxygen by non-rebreather mask at 10 to 15 l/min.
Monitor and treat, where necessary, for pulmonary oedema .
Monitor and treat, where necessary, for shock.
Anticipate seizures.
--------------------------------------------------------------
ADVANCED TREATMENT
--------------------------------------------------------------
Consider orotracheal or nasotracheal intubation for airway control in unconscious patient or where respiratory arrest has occurred.
Positive-pressure ventilation using a bag-valve mask might be of use.
Monitor and treat, where necessary, for arrhythmias.
Start an IV D5W TKO. If signs of hypovolaemia are present use lactated Ringers solution. Fluid overload might create complications.
Drug therapy should be considered for pulmonary oedema.
Hypotension with signs of hypovolaemia requires the cautious administration of fluids. Fluid overload might create complications.
Treat seizures with diazepam.
Proparacaine hydrochloride should be used to assist eye irrigation.
BRONSTEIN, A.C. and CURRANCE, P.L.
EMERGENCY CARE FOR HAZARDOUS MATERIALS EXPOSURE: 2nd Ed. 1994
Extinguishing media
SMALL FIRE: Use extinguishing agent suitable for type of surrounding fire.
LARGE FIRE: Cool cylinder.
DO NOT direct water at source of leak or venting safety devices as icing may occur.
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UNICOOL R-404A
Environmental precautions
See section 12
Other information · Do NOT store halogenated aliphatics in areas containing alkali or alkaline earth metals such as powdered
aluminum, zinc, or beryllium
Cylinders should be stored in a purpose-built compound with good ventilation, preferably in the open.
Such compounds should be sited and built in accordance with statutory requirements.
The storage compound should be kept clear and access restricted to authorised personnel only.
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UNICOOL R-404A
Cylinders stored in the open should be protected against rust and extremes of weather.
Cylinders in storage should be properly secured to prevent toppling or rolling.
Cylinder valves should be closed when not in use.
Where cylinders are fitted with valve protection this should be in place and properly secured.
+ x + o + + +
Note: Depending on other risk factors, compatibility assessment based on the table above may not be relevant to storage situations, particularly where large volumes
of dangerous goods are stored and handled. Reference should be made to the Safety Data Sheets for each substance or article and risks assessed accordingly.
Control parameters
INGREDIENT DATA
Not Available
Emergency Limits
MATERIAL DATA
Sensory irritants are chemicals that produce temporary and undesirable side-effects on the eyes, nose or throat. Historically occupational exposure standards for
these irritants have been based on observation of workers' responses to various airborne concentrations. Present day expectations require that nearly every
individual should be protected against even minor sensory irritation and exposure standards are established using uncertainty factors or safety factors of 5 to 10 or
more. On occasion animal no-observable-effect-levels (NOEL) are used to determine these limits where human results are unavailable. An additional approach,
typically used by the TLV committee (USA) in determining respiratory standards for this group of chemicals, has been to assign ceiling values (TLV C) to rapidly
acting irritants and to assign short-term exposure limits (TLV STELs) when the weight of evidence from irritation, bioaccumulation and other endpoints combine to
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UNICOOL R-404A
warrant such a limit. In contrast the MAK Commission (Germany) uses a five-category system based on intensive odour, local irritation, and elimination half-life.
However this system is being replaced to be consistent with the European Union (EU) Scientific Committee for Occupational Exposure Limits (SCOEL); this is
more closely allied to that of the USA.
May act as a simple asphyxiants; these are gases which, when present in high concentrations, reduce the oxygen content in air below that required to support
breathing, consciousness and life; loss of consciousness, with death by suffocation may rapidly occur in an oxygen deficient atmosphere.
CARE: Most simple asphyxiants are odourless or possess low odour and there is no warning on entry into an oxygen deficient atmosphere. If there is any doubt,
oxygen content can be checked simply and quickly. It may not be appropriate to only recommend an exposure standard for simple asphyxiants rather it is
essential that sufficient oxygen be maintained. Air normally has 21 percent oxygen by volume, with 18 percent regarded as minimum under normal atmospheric
pressure to maintain consciousness / life. At pressures significantly higher or lower than normal atmospheric pressure, expert guidance should be sought.
Exposure controls
Engineering controls are used to remove a hazard or place a barrier between the worker and the hazard. Well-designed
engineering controls can be highly effective in protecting workers and will typically be independent of worker interactions to
provide this high level of protection.
The basic types of engineering controls are:
Appropriate engineering
Process controls which involve changing the way a job activity or process is done to reduce the risk.
controls
Enclosure and/or isolation of emission source which keeps a selected hazard "physically" away from the worker and ventilation
that strategically "adds" and "removes" air in the work environment. Ventilation can remove or dilute an air contaminant if
designed properly. The design of a ventilation system must match the particular process and chemical or contaminant in use.
Employers may need to use multiple types of controls to prevent employee overexposure.
Individual protection
measures, such as
personal protective
equipment
Chemical goggles.
Full face shield may be required for supplementary but never for primary protection of eyes.
Contact lenses may pose a special hazard; soft contact lenses may absorb and concentrate irritants. A written policy
Eye and face protection document, describing the wearing of lenses or restrictions on use, should be created for each workplace or task. This should
include a review of lens absorption and adsorption for the class of chemicals in use and an account of injury experience.
Medical and first-aid personnel should be trained in their removal and suitable equipment should be readily available. In the
event of chemical exposure, begin eye irrigation immediately and remove contact lens as soon as practicable.
Skin protection See Hand protection below
Butyl rubber gloves
· Butyl rubber gloves should be used when handling halogenated aliphatics .
· Nitrile, PVC-coated nitrile, and PVC protective equipment are not recommended
When handling sealed and suitably insulated cylinders wear cloth or leather gloves.
Hands/feet protection
Insulated gloves:
NOTE: Insulated gloves should be loose fitting so that may be removed quickly if liquid is spilled upon them. Insulated gloves
are not made to permit hands to be placed in the liquid; they provide only short-term protection from accidental contact with
the liquid.
Body protection See Other protection below
· Halogen-selective detectors use a specialized sensor that allows the monitor to detect compounds containing
fluorine, chlorine, bromine, and iodine with-out interference from other [Link] detectors are typically easy to
use, feature higher sensitivity than the nonselective detectors (detection limits are typically <5 ppm when used as an
area monitor and <1.4 gm/yr [<0.05 oz/yr] when used as a leak pinpointer).
· Compound-Specific Detectors are typically capable of detecting the presence of a single compound without
Other protection interference from other compounds.
Protective overalls, closely fitted at neck and wrist.
Eye-wash unit.
Ensure availability of lifeline in confined spaces.
Staff should be trained in all aspects of rescue work.
Rescue gear: Two sets of SCBA breathing apparatus Rescue Harness, lines etc.
Respiratory protection
Type AX Filter of sufficient capacity. (AS/NZS 1716 & 1715, EN 143:2000 & 149:2001, ANSI Z88 or national equivalent)
Selection of the Class and Type of respirator will depend upon the level of breathing zone contaminant and the chemical nature of the contaminant. Protection
Factors (defined as the ratio of contaminant outside and inside the mask) may also be important.
Required minimum protection Maximum gas/vapour concentration present in air p.p.m. (by Half-face Full-Face
factor volume) Respirator Respirator
up to 10 1000 AX-AUS / Class1 -
up to 50 1000 - AX-AUS / Class 1
up to 50 5000 Airline * -
up to 100 5000 - AX-2
up to 100 10000 - AX-3
100+ Airline**
A(All classes) = Organic vapours, B AUS or B1 = Acid gasses, B2 = Acid gas or hydrogen cyanide(HCN), B3 = Acid gas or hydrogen cyanide(HCN), E = Sulfur
dioxide(SO2), G = Agricultural chemicals, K = Ammonia(NH3), Hg = Mercury, NO = Oxides of nitrogen, MB = Methyl bromide, AX = Low boiling point organic
compounds(below 65 degC)
Cartridge respirators should never be used for emergency ingress or in areas of unknown vapour concentrations or oxygen content.
The wearer must be warned to leave the contaminated area immediately on detecting any odours through the respirator. The odour may indicate that the mask
is not functioning properly, that the vapour concentration is too high, or that the mask is not properly fitted. Because of these limitations, only restricted use of
cartridge respirators is considered appropriate.
Cartridge performance is affected by humidity. Cartridges should be changed after 2 hr of continuous use unless it is determined that the humidity is less than
75%, in which case, cartridges can be used for 4 hr. Used cartridges should be discarded daily, regardless of the length of time used
Positive pressure, full face, air-supplied breathing apparatus should be used for work in enclosed spaces if a leak is suspected or the primary containment is to
be opened (e.g. for a cylinder change)
Air-supplied breathing apparatus is required where release of gas from primary containment is either suspected or demonstrated.
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UNICOOL R-404A
Bronchospasm consistently occurs in human subjects inhaling fluorocarbons. At a measured concentration of 1700 ppm of one
of the commercially available aerosols there is a biphasic change in ventilatory capacity, the first reduction occurring within a few
minutes and the second delayed up to 30 minutes. Most subjects developed bradycardia (reduced pulse rate).
Bradycardia is encountered in dogs when administration is limited to upper respiratory tract (oropharyngeal and nasal areas).
Cardiac arrhythmias can be experimentally induced in animals (species dependency is pronounced with dogs and monkeys
requiring lesser amounts of fluorocarbon FC-11 than rats or mice).
Acute intoxication by halogenated aliphatic hydrocarbons appears to take place over two stages. Signs of a reversible narcosis
are evident in the first stage and in the second stage signs of injury to organs may become evident, a single organ alone is
(almost) never involved.
Depression of the central nervous system is the most outstanding effect of most halogenated aliphatic hydrocarbons. Inebriation
and excitation, passing into narcosis, is a typical reaction. In severe acute exposures there is always a danger of death from
respiratory failure or cardiac arrest due to a tendency to make the heart more susceptible to catecholamines (adrenalin)
Material is highly volatile and may quickly form a concentrated atmosphere in confined or unventilated areas. The vapour may
displace and replace air in breathing zone, acting as a simple asphyxiant. This may happen with little warning of overexposure.
Symptoms of asphyxia (suffocation) may include headache, dizziness, shortness of breath, muscular weakness, drowsiness and
ringing in the ears. If the asphyxia is allowed to progress, there may be nausea and vomiting, further physical weakness and
unconsciousness and, finally, convulsions, coma and death. Significant concentrations of the non-toxic gas reduce the oxygen
level in the air. As the amount of oxygen is reduced from 21 to 14 volume %, the pulse rate accelerates and the rate and volume
of breathing increase. The ability to maintain attention and think clearly is diminished and muscular coordination is somewhat
disturbed. As oxygen decreases from 14-10% judgement becomes faulty; severe injuries may cause no pain. Muscular exertion
leads to rapid fatigue.
Not normally a hazard due to physical form of product.
Ingestion
Considered an unlikely route of entry in commercial/industrial environments
Evidence exists, or practical experience predicts, that the material either produces inflammation of the skin in a substantial
number of individuals following direct contact, and/or produces significant inflammation when applied to the healthy intact skin of
animals, for up to four hours, such inflammation being present twenty-four hours or more after the end of the exposure period.
Skin irritation may also be present after prolonged or repeated exposure; this may result in a form of contact dermatitis
(nonallergic). The dermatitis is often characterised by skin redness (erythema) and swelling (oedema) which may progress to
blistering (vesiculation), scaling and thickening of the epidermis. At the microscopic level there may be intercellular oedema of
the spongy layer of the skin (spongiosis) and intracellular oedema of the epidermis.
The material may accentuate any pre-existing dermatitis condition
Skin contact is not thought to have harmful health effects (as classified under EC Directives); the material may still produce
Skin Contact health damage following entry through wounds, lesions or abrasions.
In common with other halogenated aliphatics, fluorocarbons may cause dermal problems due to a tendency to remove natural
oils from the skin causing irritation and the development of dry, sensitive skin. They do not appear to be appreciably absorbed.
Open cuts, abraded or irritated skin should not be exposed to this material
Entry into the blood-stream through, for example, cuts, abrasions, puncture wounds or lesions, may produce systemic injury with
harmful effects. Examine the skin prior to the use of the material and ensure that any external damage is suitably protected.
Vapourising liquid causes rapid cooling and contact may cause cold burns, frostbite, even through normal gloves. Frozen skin
tissues are painless and appear waxy and yellow. Signs and symptoms of frost-bite may include "pins and needles", paleness
followed by numbness, a hardening an stiffening of the skin, a progression of colour changes in the affected area, (first white,
then mottled and blue and eventually black; on recovery, red, hot, painful and blistered).
Although the material is not thought to be an irritant (as classified by EC Directives), direct contact with the eye may produce
Eye transient discomfort characterised by tearing or conjunctival redness (as with windburn).
Direct contact with the eye may not cause irritation because of the extreme volatility of the gas; however concentrated
atmospheres may produce irritation after brief exposures..
Long-term exposure to the product is not thought to produce chronic effects adverse to health (as classified by EC Directives
Chronic using animal models); nevertheless exposure by all routes should be minimised as a matter of course.
Principal route of occupational exposure to the gas is by inhalation.
TOXICITY IRRITATION
UNICOOL R-404A
Not Available Not Available
TOXICITY IRRITATION
pentafluoroethane Inhalation (Rat) LC50: >709000 ppm4h[2] Eye: no adverse effect observed (not irritating)[1]
TOXICITY IRRITATION
Inhalation (Rat) LC50: 359453.102 ppm4h[2] Eye: adverse effect observed (irritating)[1]
1,1,1,2-tetrafluoroethane
Skin: adverse effect observed (irritating)[1]
TOXICITY IRRITATION
1,1,1-trifluoroethane
Inhalation (Rat) LC50: >540000 ppm4h[2] Not Available
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Legend: 1. Value obtained from Europe ECHA Registered Substances - Acute toxicity 2. Value obtained from manufacturer's SDS.
Unless otherwise specified data extracted from RTECS - Register of Toxic Effect of chemical Substances
PENTAFLUOROETHANE Cardiac sensitisation threshold limit >245400 mg/m3 Anaesthetic effects threshold limit 490800 mg/m3 * DuPont SDS
1,1,1,2- * with added oxygen - ZhongHao New Chemical Materials MSDS Excessive concentration can have a narcotic effect; inhalation
TETRAFLUOROETHANE of high concentrations of decomposition products can cause lung oedema.
NOTE: Substance has been shown to be mutagenic in at least one assay, or belongs to a family of chemicals producing damage
1,1,1-TRIFLUOROETHANE
or change to cellular DNA.
Disinfection by products (DBPs) re formed when disinfectants such as chlorine, chloramine, and ozone react with organic and
inorganic matter in water. The observations that some DBPs such as trihalomethanes (THMs), di-/trichloroacetic acids, and 3-
chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone (MX) are carcinogenic in animal studies have raised public concern over the
possible adverse health effects of DBPs. To date, several hundred DBPs have been identified.
Numerous haloalkanes and haloalkenes have been tested for carcinogenic and mutagenic activities. n general, the genotoxic
potential is dependent on the nature, number, and position of halogen(s) and the molecular size of the compound. Short-chain
UNICOOL R-404A & 1,1,1,2-
monohalogenated (excluding fluorine) alkanes and alkenes are potential direct-acting alkylating agents, particularly if the halogen
TETRAFLUOROETHANE
is at the terminal end of the carbon chain or at an allylic position. Dihalogenated alkanes are also potential alkylating or cross-
linking agents (either directly or after GSH conjugation),particularly if they are vicinally substituted (e.g., 1,2-dihaloalkane) or
substituted at the two terminal ends of a short to medium-size (e.g., 2-7) alkyl moiety (i.e., alpha, omega-dihaloalkane). Fully
halogenated haloalkanes tend to act by free radical or nongenotoxic mechanisms (such as generating peroxisome-proliferative
intermediates) or undergo reductive dehalogenation to yield haloalkenes that in turn could be activated to epoxides.
Haloalkenes are of concern because of potential to generate genotoxic intermediates after epoxidation.
Legend: – Data either not available or does not fill the criteria for classification
– Data available to make classification
Toxicity
Legend: Extracted from 1. IUCLID Toxicity Data 2. Europe ECHA Registered Substances - Ecotoxicological Information - Aquatic Toxicity
4. US EPA, Ecotox database - Aquatic Toxicity Data 5. ECETOC Aquatic Hazard Assessment Data 6. NITE (Japan) -
Bioconcentration Data 7. METI (Japan) - Bioconcentration Data 8. Vendor Data
On the basis of the available evidence concerning properties and predicted or observed environmental fate and behavior, the material may present a danger to the
structure and/ or functioning of the stratospheric ozone layer.
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UNICOOL R-404A
In addition to carbon dioxide (CO2), methane (CH4) and nitrous oxide (N2O), the greenhouse gases mentioned in the Kyoto Protocol include synthetic substances
that share the common feature of being highly persistent in the atmosphere and exhibiting very high specific radiative forcing (radiative forcing is the change in the
balance between radiation coming into the atmosphere and radiation out; a positive radiative forcing tends on average to warm the surface of the earth). These
synthetic substances include hydrocarbons that are partially fluorinated (HCFs) or totally fluorinated (PFCs) as well as sulfur hexafluoride (SF6).
The greenhouse potential of these substances, expressed as multiples of that of CO2, are within the range of 140 to 11,700 for HFCs, from 6500 to 9,200 for
PFCs and 23,900 for SF6. Once emitted into the atmosphere, these substances have an impact on the environment for decades, centuries, or in certain
instances, for thousands of years.
Many of these substances have only been commercialised for a few years, and still only contribute only a small percentage of those gases released to the
atmosphere by humans (anthropogenic) which increase the greenhouse effect. However, a rapid increase can be seen in their consumption and emission, and
therefore in their contribution to the anthropogenic increase in the greenhouse effect.
Since the adoption of the Kyoto Protocol, new fluorinated substances have appeared on the market, which are stable in air and have a high greenhouse potential;
these include nitrogen trifluoride (NF3) and fluoroethers.
Bioaccumulative potential
Ingredient Bioaccumulation
pentafluoroethane LOW (LogKOW = 1.5472)
1,1,1,2-tetrafluoroethane LOW (LogKOW = 1.68)
1,1,1-trifluoroethane LOW (LogKOW = 1.7393)
Mobility in soil
Ingredient Mobility
pentafluoroethane LOW (Log KOC = 154.4)
1,1,1,2-tetrafluoroethane LOW (Log KOC = 96.63)
Labels Required
Marine Pollutant NO
Shipping container, transport vehicle placarding, and labeling may vary from the below information. This depends on the quantity shipped, the applicability of
excepted quantity requirements, limited quantity requirements, and/or special provisions according to US DOT, IATA and IMDG regulations. In case of reshipment,
it is the responsibility of the shipper to determine the appropriate labels and markings in accordance with applicable transport regulations.
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UNICOOL R-404A
14.5. Environmental
Not Applicable
hazard
14.7.1. Transport in bulk according to Annex II of MARPOL and the IBC code
Not Applicable
14.7.2. Transport in bulk in accordance with MARPOL Annex V and the IMSBC Code
Product name Group
pentafluoroethane Not Available
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UNICOOL R-404A
Safety, health and environmental regulations / legislation specific for the substance or mixture
International Agency for Research on Cancer (IARC) - Agents Classified by the IARC Monographs - Not Classified as Carcinogenic
US AIHA Workplace Environmental Exposure Levels (WEELs)
US DOE Temporary Emergency Exposure Limits (TEELs)
US EPA Integrated Risk Information System (IRIS)
US Toxic Substances Control Act (TSCA) - Chemical Substance Inventory
US Toxicology Excellence for Risk Assessment (TERA) Workplace Environmental Exposure Levels (WEEL)
Federal Regulations
Explosive No
Self-heating No
Corrosive to metal No
Oxidizer (Liquid, Solid or Gas) No
Organic Peroxide No
Self-reactive No
Carcinogenicity No
Aspiration Hazard No
Germ cell mutagenicity No
US. EPA CERCLA Hazardous Substances and Reportable Quantities (40 CFR 302.4)
None Reported
US. EPCRA Section 313 Toxic Release Inventory (TRI) (40 CFR 372)
None Reported
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UNICOOL R-404A
State Regulations
CONTACT POINT
- For quotations contact your local Customer Services - [Link] - - Responsible for safety data sheet Wilhelmsen
Ships Service AS - Prepared by: Compliance Manager, - Email: Email: [Link]@[Link] - Telephone: Tel.: +47 67584000
5.7 29/03/2023 Identification of the substance / mixture and of the company / undertaking - Synonyms
Other information
Classification of the preparation and its individual components has drawn on official and authoritative sources as well as independent review by the Chemwatch
Classification committee using available literature references.
The SDS is a Hazard Communication tool and should be used to assist in the Risk Assessment. Many factors determine whether the reported Hazards are Risks
in the workplace or other settings. Risks may be determined by reference to Exposures Scenarios. Scale of use, frequency of use and current or available
engineering controls must be considered.
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UNICOOL R-404A
end of SDS