Degreaser cleaner makes oil soluble in water. Degreaser higher concentration not only resulting oil cleaning effect smoothly but also its costing less in terms of area covered per unit wise.
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Degreaser Cleaner is specialized Oil greaser deposited cleaning product, Which is effectively cleans grease, oils, cutting fluids, greasy soils, prints, and other greasy contamination.

| Product Name |
Degreaser |
| Part Number | RXSOL-41-8649-025 |
Company Details:
RX MARINE INTERNATIONAL
105, A wing , BSEL , TECH PARK.
VASHI ,NEW BOMBAY 400703 INDIA
Branch : Kandla, Mumbai, Vizag, Chennai, Kolkata Fujairah UAE and Oman
| Phone | +91 22 27815540 / 41 / 42 |
| Fax | +91 22 2781 1318 :::AOH :0091 9821214367 |
| 123@rxmarine.com | |
| Website | www.rxmarine.com |

| Name of Substance | Cas Number | EC Number | Weight % |
| Natural Alcohol | 64-17-5 | 200-578-6 | 70 - 60% |
| MEK | 78-93-3 | 201-59-0 | 10-20 |
| Surfactant |
Proprietary |
20 -30% |

| Signal word | Water Soluble |
| Hazard statement(s) |
H319 Causes serious eye irritation. |
| Precautionary statements |
P210: Keep away from heat / sparks / open flames / hot surfaces ‒ No smoking. P233: Keep container tightly closed. P240: Ground/bond container and receiving equipment. P241: Use explosion-proof electrical / ventilating / lighting equipment. P242: Use only non-sparking tools. P243: Take precautionary measures against static discharge. P280: Wear protective gloves / protective clothing /eye protection. P264: Wash skin thoroughly after handling. P303+ P361+P353: If on skin or hair remove/ take off immediately all contaminated clothing. Rinse skin with water. P305+P351+P338: IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P337+P313: If eye irritation persists: Get medical advice/attention. P370 + P378: In case of fire: Use powder, alcohol-resistant foam, lots of water, carbon dioxide for extinction. P403 + P235: Store in a well-ventilated place. Keep cool. P501:Disposal: Dispose of contents / container to a specialised waste disposal plant in accordance with local / regional regulations |
| Main Hazard | Harmful if swallowed or inhaled. Possible aspiration hazard if swallowed (can enter lungs and cause damage). May be irritating to the skin, eyes and respiratory tract. Over exposure may cause CNS depression. Possible reproductive hazard. |
| Health effects – eyes | Moderately irritating. Exposure to liquid, vapours, fumes or mist may cause irritation. Direct contact may cause irritation, redness, pain, corneal inflammation and possible corneal damage. |
| Health effects – skin | Repeated or prolonged contact may result in defatting, redness, pain, itching, inflammation, cracking and possible secondary infection. Repeated skin contact may result in allergic skin reaction in a very small proportion of individuals. |
| Health effects – ingestion |
Large doses lead to poisoning while repeated ingestion can lead to alcoholism. Alcohol abuse and dependence can have a profound effect on work performance and tendency to accidents at work.11-13 The presence of denaturants and surgfactant |
| Health effects – inhalation | Intoxicating if continuously inhaled for a long period of time. Occupational Exposure Limits (8-hour reference period) 1000ppm (1900mg/m3 ).30May cause respiratory tract irritation. |
| Carcinogenicity | Long-term consumption of alcoholic beverages demonstrates an increase in the occurrence of breast cancer and colorectal cancer. Malignant tumours of the oral cavity, Pharynx, Larynx, Oesophagus and Liver is also causally related to the consumption of alcoholic beverages.31 Some studies20, 21 have shown an excess incidence of laryngeal cancer over the expected from exposure to synthetic alcohol, with Diethyl Sulphate probably being the causative agent |
| Mutagenicity | Ethanol has been found to be non- mutagenic in the Salmonella microsome test, 22 but some transient mutagenic changes have been observed in male, but not female, mice treated with rather large doses.23-25 Ethanol is mutagenic in man via its first metabolite, Acetaldehyde. Acetaldehyde induces chromosomal aberrations, sister-chromatid exchanges and cross-links between DNA strands.32 |
| Neurotoxicity | Over exposure may cause Central Nervous System (CNS) depression |

| Product in eye | Flush immediately with water or neutral saline solution for at least 15 minutes. Seek medical attention. |
| Product on skin | Remove contaminated clothing and rinse contaminated area with soap and water. If skin irritation persists, seek medical attention. |
| Product ingested | If victim is conscious, give 1-3 glasses of water or milk to dilute stomach contents. If spontaneous vomiting occurs, or when vomiting is induced, monitor for breathing difficulty. Do not make an unconscious or semi – conscious person vomit. Keep affected person warm at rest. Get medical attention for substantial ingestions and/or gastrointestinal symptoms. |
| Product inhaled | Remove the victim to fresh air. If not breathing, ensure open airway and institute cardiopulmonary resuscitation (CPR). If breathing is weak, irregular or has stopped apply artificial respiration. Oxygen may be beneficial. Keep affected person warm and at rest. Get immediate medical attention. |

| Extinguishing media | Use dry chemical, alcohol foam or carbon dioxide to extinguish fire. Water may be ineffective but should be used to cool fire- exposed containers, structures and to protect personnel. If leak or spill has not ignited, ventilate area and use water spray to disperse gas or vapour and to protect personnel attempting to stop a leak. Use water to dilute spills and to flush them away from sources of ignition. Do not flush down public sewers or other drainage systems. |
| Special Hazards |
Vapours form flammable or explosive mixtures with air at room temperature. Vapour or gas may spread to distant ignition sources and flash back. Run – off to sewer may cause fire or explosion hazard. Containers may explode in heat of fire. Vapours may concentrate in confined areas. Irritating or toxic substances may be emitted upon thermal decomposition. Hazardous composition products such as carbon oxides may form. |
| Protective clothing | Exposed fire fighters should wear approved self-contained breathing apparatus with full face mask and full protective equipment. |

| Personal precautions |
Exposed fire fighters should wear approved self-contained breathing apparatus with full face mask and full protective equipment. |
| Enviromental Precautions | Prevent liquid entering sewers. Do not allow to enter surface waters, storm drains, etc. |
| Small spills | Take immediate steps to stop and contain the spill. Caution should be excised regarding personnel safety and exposure to be spilled material. Eliminate all sources of ignition and wear protective clothing. Absorb small spills onto paper towels and evaporate in a safe place e.g. in a fume hood. Flush the contaminated area with plenty of water. |
| Large spills | Stop leak if you can do it without risk. Contact your local fire department. Eliminate all sources of ignition and static; restrict access to area until completion of clean-up procedure. Wear adequate protective equipment, use self-contained breathing apparatus in confined poorly-ventilated areas. Large quantities should be absorbed on to sand, vermiculite or an equivalent absorbent material and removed to a safe area for disposal. Flush the contaminated area with plenty of water. Incineration is the recommended method of disposal |

| Suitable material | It is is not corrosive to metals and may be stored in stainless steel, mild steel or aluminiumcontainers. It may also be stored in HDPE containers. |
| Handling/ storage precautions | Ground lines and equipment used during transfer to reduce the possibility of static spark-initiated fire or explosion. Store in approved flammable liquid storage containers. Keep containers tightly closed as this material readily absorbs moisture. Store away from incompatible materials. Store in a cool, dry well ventilated area away from sparks, flames and other sources of ignition. Eliminate all sources of static electricity. Use non sparking electrical and ventilation systems. |

| Engineering Control | Engineering control methods to reduce hazardous exposures are preferred. General methods include mechanical ventilation dilution and local exhaust, process or personnel enclosure, control of process conditions and process modification e.g. substitution of a less hazardous material. Administrative controls and personal protective equipment may also be required. Use a non-sparking, grounded ventilation system separate from other exhaust ventilation systems. Exhaust directly to the outside. Supply sufficient replacement air to make up for air removed by exhaust system. | |||||||||||||||||||||
| Personal Protection Respiratory | If exposure limits are exceeded or if irritation is experienced, an approved respirator for organic vapours is generally acceptable. For high concentrations and for oxygen-deficient atmospheres, use approved air- supplied respirator. Full respiratory protection should be readily available in case ofspillage. | |||||||||||||||||||||
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Exposure Limits: |
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| Personal protection – hand | Rubber (Butyl) or neoprene gloves are recommended. | |||||||||||||||||||||
| Personal protection – eye | Prevent eye contact with this material. Wear chemical tight safety goggles where eye exposure is reasonably probable. Provide an eyewash station immediately accessible to the work area. Contact lenses should not be worn when working with this chemical. | |||||||||||||||||||||
| Personal protection – skin | Avoid skin contact. When working with this substance, wear appropriate chemical protective gloves. Wear protective suit/ overalls. Depending upon conditions of use, additional protection may be necessary such as face shield, apron, etc. | |||||||||||||||||||||
| Other protection | Provide a safety shower immediately accessible to the work area. |

| Appearance | Colourless, liquid |
| Odour | Characteristic pleasant odour |
| pH | Neutral |
| Boiling point | 98⁰C - 80⁰C |
| Melting point | - 130⁰C to - 112⁰C |
| Flash point | 82⁰C |
| Auto-flammability | 450⁰C |
| Explosive properties | Vapours can form explosive mixtures with air. All sources of ignition or static must be. |
| excluded. Oxidizing properties | None |
| Vapour pressure | 59 mm Hg at 20⁰C |
| Density | 0.80 kg/m3 – 0.809 kg/m3 at 25⁰C |
| Solubility – water | Miscible with water in all proportions |
| Solubility – solvent | Miscible with ether, methanol, chloroform and acetone |
| Solubility – coefficient | 1100 @ 37⁰C33 |

| Recativity | Stable at normal ambient temperature and pressure. |
| Chemical Stability | No decomposition if stoned and applied as directed. |
| Incompatible materials | See section 3 (chemical hazards). |
| Hazardous decomposition products |
Incomplete combustion can generate carbon monoxide and carbon dioxide |
| Condition to Avoid | Overheating, flames, sources of ignition or static electricity. Oxidizing agents. Vapour/ air mixtures are explosive. Keep away from heat and sources of ignition. |

| Acute toxicity |
Short-term hazards Acute oral toxicity Ethanol : LD50 rat: 7,060 mg/kg; literature value Acute inhalation toxicity Ethanol : LC50 rat: 66,000 mg/l; literature value; 4 h Acute dermal toxicity Ethanol : LDLo rabbit: 20,000 mg/kg; literature value NOAEL - 2400 mg/kg (2%) - for rats LOAEL – 3600 mg/kg (3%) - for rats |
| Skin and eye contact |
Redness, pain (refer to Section 3 for further information) |
| Chronic toxicity | Refer to Section 3. |
| Carcinogenicity | Refer to Section 3 |
| Mutagenicity | Refer to Section 3 |
| Neurotoxicity | Refer to Section 3 |
| Reproductive hazards | Refer to Section 3 |

| Aquatic toxicity – fish | In high concentration it harms fish and plankton; LC50 (fish, 96 hours) – 15.3 mg/L (Pimephales promelas) |
| Aquatic toxicity – daphnia | Threshold for deleterious effects in small crustaceans upwards of 7.800 mg/l; EC50 (Daphnia, 48 hours) – 5012 mg/L (Ceriodaphnia dubia) |
| Aquatic toxicity – algae | Toxic threshold concentration: Pseudomonas putida upwards of 6.500mg/l, Scenedesmus quadricauda upwards of 5.000mg/l, Microsystis aeruginosa upwards of 1.450ml/L |
| Biodegradability |
IC50 (algae, 72 hours) – 275 mg/L This product is readily biodegradable. Ethanol is widely recognized as being readily biodegradable in the environment as it is both a metabolite of and nutrient for microbes. There are no persistent. |
| Bio – accumulation | This product in not expected to bio accumulate through the food chains in the environment. The very low log KOW of –0.31 is indicative of a low bioaccumulation potentia. |
| Mobility | This product is likely to volatize rapidly into the air because of its high vapour pressure. The product is poorly absorbed onto soils or sediments. Adsorption coefficient (KOC) solid phase/liquid phase = 1 (highly mobile) |
| German wgk | 1 (low hazard to water) |

| Disposal methods | Only under conditions approved by local authorization. See also Section 6. |
| Disposal of packaging | Empty containers may contain flammable and hazardous residues. Always obey hazard warnings. |

| ADR/RID class | 3 |
| ADR/RID item No | 3(b) |
| ADR/RID hazard identity No | 3 |
| IMDG – shipping name |
Non Corrosive, Degreaser |
| IMDG – class | 3 |
| IMDG – packaging group | II |
| IMDG – marine pollutant | Not a marine pollutant |
| IMDG – EMS No | F-E, S-D |
| IMDG – MFAG table No | 3074 |
| IATA – shipping name |
Non Corrosive, Degreaser |
| IATA – class | 3 |
| IATA – subsidiary risk(s) | - |
| ADNR – class | Class 3, Packaging Group II |
| UK – description | Not available |
| UK- emergency action class | Not available |
| UK – classification | Not available |
| Tremcard No | 1170 |

| EEC hazard classification | 200 – 578 - 6 |
| Risk phases | R11 |
| Safety phases | S2, S7, S9, S16, S33 |
| National legislation |
Hazardous Substances Act 15 of 1973 and Regulations Occupational Health and Safety Act 85 of 1993 (Hazardous Chemical Substances Regulations) |
| International Legislation |
IATA Dangerous Goods Regulation (DGR) 59th Edition 2018 IMDG Code, International Maritime Dangerous Goods Code, 2008 Edition, Volume 1 and 2 |

| Other Information |
The information above is believed to be accurate and represents the best information currently available to us. However, we make no warranty of merchantability or any other warranty, express or implied, with respect to such information, and we assume no liability resulting from its use. Users should make their own investigations to determine the suitability of the information for their particular purposes. In no event shall be liable for any claims, losses, or damages of any third party or for lost profits or any special, indirect, incidental, consequential or exemplary damages, howsoever arising, even if RX Marine International has been advised of the possibility of such damages. DISCLAIMER OF LIABILITY :The information in this SDS was obtained from sources which we believe are reliable. However, the information is provided without any warranty, express or implied, regarding its correctness. The conditions or methods of handling, storage, use or disposal of the product are beyond our control and may be beyond our knowledge. For this and other reasons, we do not assume responsibility and expressly disclaim liability for loss, damage or expense arising out of or in any way connected with the handling, storage, use or disposal of the product. This MSDS was prepared and is to be used only for this product. If the product is used as a component in another product, this MSDS information may not be applicable. |