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Picric Acid Manufacturers

Anmol Chemicals Group, established in 1976, is the pioneer manufacturer of Specialty chemicals, Pharmaceutical Excipients, Fragrance & Flavor chemicals in India. Anmol Chemicals Group has manufacturing facilities spread across Western India, representatives in Houston Chicago USA and toll manufacturers in China. We also have toll manufacturing units for processing chemicals in a few countries around the world. We make IP, BP, USP, Ph. Eur., FCC or Food Grade, ACS, AR or Analytical Reagent Grade, LR or Laboratory Reagent Grade, Pure and Technical Grades of various chemicals. All our items are analyzed to meet the required standards.

Our manufacturing facility is FDA approved and cGMP, ISO-9001, ISO-14001, ISO OHSAS 18000, ISO 22000-2005 HACCP, FSSAI, FSSC-22000, certified. Apart from good manufacturing practice, we also follow good laboratory practice. We are offering products manufactured as per Kosher and Halal approved certified method. We are pre-registered with "Reach" for export to European countries. We can give all solid chemical materials as per specified size or shape.

Exporter Importer by Sea Exports by Air Chemical Exporter. Palletized for Export. Liquid Products HDPE Drum Packing of Chemicals Bulk Export Packing Jumbo Bag Packing

Picric acid

Synonyms: ----
CAS Number: 88-89-1, Molecular Weight: 229.10, Chemical Formula: C6H3N3O7, EINECS EC Number: 201-865-9, FEMA: ----,

Picric acid is an organic compound with the formula (O2N)3C6H2OH. Its IUPAC name is 2,4,6-trinitrophenol (TNP). The name "picric" comes from the Greek meaning "bitter", reflecting its bitter taste. It is one of the most acidic phenols. Like other highly nitrated organic compounds, picric acid is an explosive, which was once its primary use. It has also been used in medicine (antiseptic, burn treatments) and dyes.

Picric Acid is distributed by the manufacturers wet with 10 to 35% water. As the water evaporates over time, the substance becomes dry picric acid crystals. Dry picric acid is highly explosive especially when it is combined with. It will also react with alkaline materials including plaster and concrete to form explosive materials. This material is shock sensitive and corrosive to metal containers.

Specification ---------------- General Grade ---------- LR Grade
Appearance ------------------ ----------- Lemon Yellow -----------
Assay: ------------------------ 98% ---------------------- 99,5%
Sulphate (SO4): ------------- 02% ---------------------- 0.05%
Melting range: --------------- 118-120°C ------------- 119-123°C
Insoluble and resinous matter: ------ ------------------- 0.2%
Analysis applied to the dry substance, Water added as agreed.

Picric acid SDS MSDS Sheet, Material Safety Data Sheet


PRODUCT NAME: Picric acid
PRODUCT USE: Used as a laboratory reagent and in industries.
Recommended usage: Industrial Manufacturing.


Explosives Division 1.1
Flammable solids Category 1
Self-reactive substances and mixtures Type B
Acute oral toxicity Category 3
Acute dermal toxicity Category 3
Serious eye damage/eye irritation Category 1
Acute Inhalation Toxicity - Vapors Category 3

GHS, Globally Harmonized System Classification in accordance with 29 CFR 1910

GHS Label Elements
GHS Label Elements
GHS Label Elements

Signal Words: Danger

Hazard statements:
H201 Explosive; mass explosion hazard
H228: Flammable solid
H241: Heating may cause a fire or explosion.
H301: Toxic if swallowed.
H311: Toxic in contact with skin.
H319 Causes serious eye irritation.
H331: Toxic if inhaled.

Precautionary statements:
P210: Keep away from heat/sparks/open flames/hot surfaces – No smoking.
P220 : Keep away from heat/sparks/open flames/hot surfaces – No smoking.
P230 :Keep wetted with water.
P234+235: Keep cool in original container only.
P240: Ground/bond container and receiving equipment.
P241 : Use explosion-proof electrical/ventilating/light/equipment.
P250: Do not subject to grinding/shock/friction.
P261: Avoid breathing dust/ fume/ gas/ mist/ vapors/ spray.
P262: Do not get in eyes, on skin, or on clothing.
P264: Wash skin thoroughly after handling.
P270: Do not eat, drink or smoke when using this product.
P271: Use only outdoors or in a well-ventilated area.
P280: Wear protective gloves/protective clothing/eye protection/face protection. P372: Explosion risk in case of fire.
P373: DO NOT fight fire when fire reaches explosives.
P301+310: IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.
P302+352: IF ON SKIN: Wash with soap and water.
P304+340: IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing.
P305+P351+P338: IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P370+P378: In case of fire: Use water spray, fog or foam, dry chemical, CO2 for extinction.
P370+P380+375: In case of fire: Evacuate area. Fight fire remotely due to the risk of explosion.
P312: Call a POISON CENTER or doctor/physician if you feel unwell.
P314: Get Medical advice/attention if you feel unwell.
P330: Rinse mouth.
P337+P313: If eye irritation persists: Get medical advice/ attention.
P361: Remove/Take off immediately all contaminated clothing.
P362: Take off contaminated clothing and wash before reuse.
P401: Store diluted with water.
P403+P233: Store in a well ventilated place. Keep container tightly closed.
P403+P235: Store in a well ventilated place. Keep cool.
P420 : Store away from other materials.
P501: Dispose of contents/ container to an approved waste disposal plant.


NAME: Picric Acid in water. water not less than 30%.
CAS: 88-89-1
EINECS EC Number: 201-865-9
PERCENT: 97-100% diluted with water Containing not less than 30% water: for safety) 


Always seek medical attention after first aid measures are provided.

Where Medical attention is not immediately available or where the patient is more than 15 minutes from a hospital or unless instructed otherwise:
For advice, contact a Poisons Information Center or a doctor.
Urgent hospital treatment is likely to be needed.
If conscious, give water to drink.
INDUCE vomiting with fingers down the back of the throat, ONLY IF CONSCIOUS. Lean patient forward or place on left side (head-down position, if possible) to maintain open airway and prevent aspiration.
NOTE: Wear a protective glove when inducing vomiting by mechanical means. In the mean time, qualified first-aid personnel should treat the patient following observation and employing supportive measures as indicated by the patient's condition. If the services of a medical officer or medical doctor are readily available, the patient should be placed in his/her care and a copy of the MSDS should be provided. Further action will be the responsibility of the medical specialist. If medical attention is not available on the worksite or surroundings send the patient to a hospital together with a copy of the MSDS.

If this product comes in contact with the eyes, immediately hold eyelids apart and flush the eye continuously with running water. Ensure complete irrigation of the eye by keeping eyelids apart and away from eye and moving the eyelids by occasionally lifting the upper and lower lids. Continue flushing until advised to stop by the Poisons Information Center or a doctor, or for at least 15 minutes. Transport to hospital or doctor without delay. Removal of contact lenses after an eye injury should only be undertaken by skilled personnel.

If skin or hair contact occurs, quickly but gently, wipe material off skin with a dry, clean cloth. Immediately remove all contaminated clothing, including footwear. Wash skin and hair with running water. Continue flushing with water until advised to stop by the Poisons Information Center. Transport to hospital, or doctor.

If fumes or combustion products are inhaled remove from contaminated area. Lay patient down. Keep warm and rested. Prostheses such as false teeth, which may block airway, should be removed, where possible, prior to initiating first aid procedures. Apply artificial respiration if not breathing, preferably with a demand valve resuscitator, bag-valve mask device, or pocket mask as trained. Perform CPR if necessary. Transport to hospital, or doctor, without delay.


Vapor Pressure (mmHG): < 0.26 @ 195C
Specific Gravity (water=1): 1.76 (anh.)

For SMALL FIRES: Dry chemical, CO2, water spray or foam.
For LARGE FIRES: Water-spray, fog or foam.

Alert Emergency Responders and tell them location and nature of hazard. Wear breathing apparatus plus protective gloves. Prevent, by any means available, spillage from entering drains or water course. Fight fire from a safe distance, with adequate cover. If safe, switch off electrical equipment until vapor fire hazard removed. Use water delivered as a fine spray to control fire and cool adjacent area. Avoid spraying water onto liquid pools.
DO NOT approach containers suspected to be hot. Cool fire exposed containers with water spray from a protected location. If safe to do so, remove containers from path of fire.

Detonation may occur from heavy impact or excessive heating.
Mixing with incompatible chemicals may cause expansion, decomposition or detonation.
Heat affected containers remain hazardous.
Explosives can supply own oxygen for combustion and smothering action of foam or dry chemical may be ineffective.
Combustion or decomposition produces oxides of nitrogen (NOx), carbon monoxide (CO) and carbon dioxide (CO2).

Avoid contamination with oxidizing agents i.e. nitrates, oxidizing acids, chlorine bleaches, pool chlorine etc. as ignition may result.


MINOR SPILLS: Remove all ignition sources. DO NOT touch or walk through spilled material. Clean up all spills immediately. Avoid contact with skin and eyes. Prevent dust cloud. With clean shovel (preferably non-sparking) place material into clean, dry container and cover loosely. Move containers from spill area. Control personal contact by using protective equipment.

MAJOR SPILLS: Clear area of personnel and move upwind. Alert Emergency Responders and tell them location and nature of hazard. DO NOT touch or walk through spilled material. Control personal contact by using protective equipment. Prevent, by any means available, spillage from entering drains or water course. No smoking, naked lights or ignition sources. Increase ventilation. Stop leak if safe to do so. Contain or cover with sand, earth or vermiculite. Use only spark-free shovels and explosion proof equipment. Collect recoverable product into labeled containers for recycling. Collect solid residues and seal in labeled drums for disposal. Wash area with water and dike for later disposal; prevent runoff into drains. After clean up operations, decontaminate and launder all protective clothing and equipment before storing and re-using. If contamination of drains or waterways occurs, advise emergency services.


Outside or detached storage is preferred
Containers should be bonded and grounded for transfers to avoid sparks
Use non-sparking tools and equipment including explosion proof ventilation
Store in glass NOT metals containers and wet screw tops before sealing
Do not store on concrete floors or wooden pallets
Enclose all processes and employ automatic mechanical handling techniques and wet methods where possible
If handling picric acid contained in a jar, gently tilt bottle to see if crystals roll over each other - if they do the acid is dry and capable of explosion - contact personnel trained in the handling of explosives immediately
Dry crystals may be present in the threads of screw top containers and present a detonation hazard when opening the container
Containers of this material remain hazardous when empty since they retain product residues - observe all warnings for the product
Avoid all personal contact, including inhalation.
Wear protective clothing when risk of overexposure occurs.
Use in a well-ventilated area.
Prevent concentration in hollows and sumps.
DO NOT enter confined spaces until atmosphere has been checked.
DO NOT allow material to contact humans, exposed food or food utensils.
Avoid smoking, naked lights or ignition sources.
When handling, DO NOT eat, drink or smoke.
Avoid contact with incompatible materials.
Keep containers securely sealed when not in used.
Avoid physical damage to containers.
Always wash hands with soap and water after handling.
Working clothes should be laundered separately. Launder contaminated clothing before re-use.
Use good occupational work practice.

DO NOT use unlined steel containers
Store in a dark glass or other suitable light resistant container.
For low viscosity materials and solids: Drums and jerricans must be of the non-removable head type. Where a can is to be used as an inner package, the can must have a screwed enclosure. For materials with a viscosity of at least 2680 cSt. (23 deg. C):
Removable head packaging and cans with friction closures may be used.
Where combination packages are used, there must be sufficient inert absorbent material to absorb completely any leakage that may occur, unless the outer packaging is a close fitting molded plastic box and the substances are not incompatible with the plastic. All combination packages for Packing group I and II must contain cushioning material.

FOR MINOR QUANTITIES: Store in an indoor fireproof cabinet or in a room of noncombustible construction Provide adequate portable fire-extinguishers in or near the storage area.
FOR PACKAGE STORAGE: Store in original containers in approved flame-proof area. No smoking, naked lights, heat or ignition sources. DO NOT store in pits, depressions, basements or areas where vapors may be trapped. Keep containers securely sealed. Store away from incompatible materials in a cool, dry well ventilated area. Protect containers against physical damage and check regularly for leaks.

Protect containers from exposure to weather and from direct sunlight unless: (a) the packages are of metal or plastic construction; (b) the packages are securely closed are not opened for any purpose while in the area where they are stored and (c) adequate precautions are taken to ensure that rain water, which might become contaminated by the dangerous goods, is collected and disposed of safely. Ensure proper stock-control measures are maintained to prevent prolonged storage of dangerous goods.


Exposure Limits

Chemical Name ACGIH --------- and NIOSH ----------------------------- and OSHA - Final PELs
Picric acid CAS-No. 88-89-1 0.1 mg/m3 TWA and 0.1 mg/m3 TWA 75 mg/m3 IDLH and 0.1 mg/m3 TWA

The TLV-TWA is thought to be protective against the development of systemic toxicity but may not, however, prevent the development of dermatitis or sensitization in some workers exposed at the 8-hour TWA.

Respirators may be necessary when engineering and administrative controls do not adequately prevent exposures.
The decision to use respiratory protection should be based on professional judgment that takes into account toxicity information, exposure measurement data, and frequency and likelihood of the worker's exposure - ensure users are not subject to high thermal loads which may result in heat stress or distress due to personal protective equipment (powered, positive flow, full face apparatus may be an option).
Use approved positive flow mask if significant quantities of dust becomes airborne.
Try to avoid creating dust conditions.
Use appropriate NIOSH-certified respirator based on informed professional judgment. In conditions where no reasonable estimate of exposure can be made, assume the exposure is in a concentration IDLH and use NIOSH-certified full face pressure demand SCBA with a minimum service life of 30 minutes, or a combination full face piece pressure demand SAR with auxiliary self-contained air supply. Respirators provided only for escape from IDLH atmospheres shall be NIOSH-certified for escape from the atmosphere in which they will be used.

Local exhaust ventilation usually required. If risk of overexposure exists, wear an approved respirator. Correct fit is essential to obtain adequate protection an approved self contained breathing apparatus (SCBA) may be required in some situations. Provide adequate ventilation in warehouse or closed storage area.
Air contaminants generated in the workplace possess varying "escape" velocities which, in turn, determine the "capture velocities" of fresh circulating air required to effectively remove the contaminant.
For large scale or continuous use:
Spark-free, earthed ventilation system, venting directly to the outside and separate from usual ventilation systems Provide dust collectors with explosion vents


Appearance: Yellow crystals with a very bitter taste supplied in water as paste. Becomes Explosive when dry. Soluble in alcohol, ether, acetone, benzene, acetic acid.
Molecular Weight: 229.11 anhydrous
Melting Range (°F): 251.6
Viscosity: Not Available
Boiling Range (°F): explodes >572F
Solubility in water (g/L): Partly Miscible
Autoignition Temp (°F): 572 (explodes)
Vapor Pressure (mmHG): < 0.26 @ 195C
Upper Explosive Limit (%): Not available
Specific Gravity (water=1): 1.76 (anh.)
Relative Vapor Density (air=1): 7.91 (anh.)
Volatile Component (%vol): Not available Evaporation Rate Not available


Stable under recommended storage conditions.

Presence of shock and friction
Presence of heat source and ignition source
Presence of incompatible materials.
Product is considered stable.
Hazardous polymerization will not occur.

Picric acid when dry is a highly unstable and heat, friction-, and impact- sensitive explosive (explodes at approximately 300 C) explosive sensitivity increases when trace metals are present reacts with nitric acid, alkalis, heavy metals, copper, lead, zinc, transition metals, and other metals and their salts, to form other salts known as picrates; these are initiators which are much more highly sensitive to heat, impact, or shock than the parent compound – shock sensitive salts include ammonium salts and calcium salts (the calcium salt may be produced when picric acid comes in contact with plaster or concrete - do NOT store on uncoated concrete) mixtures with perchlorates form extremely powerful, high velocity explosives reacts violently with strong oxidizers is incompatible with ammonia may accumulate static electric charge, when dry, producing explosion is a strong oxidizer in aqueous solution and a strong acid reacts violently with alkalis, reducing agents, combustible materials, organic materials and other easily oxidized materials, aluminium powders, and other metal powders attacks many materials, forming flammable hydrogen gas attacks natural rubber, polyvinyl alcohol, PVC, Polynitro derivatives of mono- and poly- cyclic systems are often explosives liable to detonate on grinding or impact. The presence of two or more nitro groups (each with 2 oxygen atoms) on an aromatic nucleus often increase the reactivity of other substituents and the tendency towards explosive instability as oxygen balance is approached. Aromatic nitro compounds range from slight to strong oxidizing agents. If mixed with reducing agents, including hydrides, sulfides and nitrides, they may begin a vigorous reaction that culminates in a detonation. The explosive tendencies of aromatic nitro compounds are increased by the presence of multiple nitro groups.

In view of the reports of previous violent or explosive reactions, heating of polynitroaryl (particularly di- and tri-nitroaryl) compounds with alkalies, ammonia, or O-ethylsulfuric acid salts, in autoclaves should be avoided.

Nitroaromatic and in particular polynitroaromatic compounds may present a severe explosion risk if subjected to shock or heated rapidly and uncontrollably as in fire situations. In addition, when such compounds are heated more moderately with caustic alkalies, even when water or organic solvents are present, there is also a risk of violent decomposition or explosion. Several industrial accidents, which probably were due to such interactions, have occurred; this potential hazard often remains unacknowledged.

A range of exothermic decomposition energies for nitro compounds is given as 220-410 kJ/mol. The relationship between energy of decomposition and processing hazards has been the subject of discussion; it is suggested that values of energy released per unit of mass, rather than on a molar basis (J/g) be used in the assessment. For example, in "open vessel processes" (with man-hole size openings, in an industrial setting), substances with exothermic decomposition energies below 500 J/g are unlikely to present a danger, whilst those in "closed vessel processes" (opening is a safety valve or bursting disk) present some danger where the decomposition energy exceeds 150 J/g.

Avoid reaction with oxidizing agents, bases and strong reducing agents.


Oral (rat) LD50: 200 mg/kg Nil Reported
Intraperitoneal (mouse) LD50: 56.3 mg/kg
Oral (rabbit) LDLo: 120 mg/kg
Oral (cat) LDLo: 250 mg/kg

Routes of Entry: Absorbed through skin. Inhalation. Ingestion.
MUTAGENIC EFFECTS: Mutagenic for bacteria and/or yeast. Causes damage to the following organs: mucous membranes.


Fish LC50 (96hr.) (mg/l): 30
Daphnia magna EC50 (48hr.) (mg/l): 88
log Pow (Verschueren 1983): 2.03

COD: 0.92
ThOD: 0.98
Half- life Soil - High (hours): 4320
Half- life Soil - Low (hours): 672
Half- life Air - High (hours): 4320
Half- life Air - Low (hours): 672
Half- life Surface water - High (hours): 4320
Half- life Surface water - Low (hours): 672
Half- life Ground water - High (hours): 8640
Half- life Ground water - Low (hours): 48
Aqueous biodegradation - Aerobic - High (hours): 4320
Aqueous biodegradation - Aerobic - Low (hours): 672
Aqueous biodegradation - Anaerobic - High (hours): 300
Aqueous biodegradation - Anaerobic - Low (hours): 48
Aqueous photolysis half- life - High (hours): 360
Photooxidation half- life air - High (hours): 4320
Photooxidation half- life air - Low (hours): 677
Harmful to aquatic organisms.

The nitrates are of environmental concern because of their high water solubility and consequent leaching, diffusion, and environmental mobility in soil and water. Nitrate can contaminate groundwater to unacceptable levels. Nitrite is formed from nitrate or ammonium ion by micro-organisms in soil, water, sewage and the alimentary tract. The concern with nitrate in the environment is related to its conversion to nitrite. Methemoglobinemia is caused following exposure to high levels of nitrite and produces difficulties in oxygen transport in the blood. Thousands of cases involving poisoning of infants, particularly in rural areas, have been reported as a result of drinking nitrate rich well-water. Other concerns deriving from exposure to environmental nitrates relate to the production of nitrosamines following the reaction of food nitrites and secondary amines. Other nitroso-compounds may result following reaction with nitrites and amides, ureas, carbamates and other nitrogenous compounds. Nitrosamines produce liver damage, hemorrhagic lung lesions, convulsions and coma in rats, and teratogenic effects in experimental animals.

The N-nitroso class of compounds include potent carcinogens and mutagens: induction of tumors by single doses of N-nitroso compounds testify to this.

DO NOT discharge into sewer or waterways.

Products of Biodegradation: Possibly hazardous short/long term degradation products are to be expected.
Toxicity of the Products of Biodegradation: The products of degradation are less toxic than the product itself.

This substance/mixture contains no components considered to be either persistent, bioaccumulative and toxic (PBT), or very persistent and very bioaccumulative (vPvB) at levels of 0.1% or higher.


US EPA Waste Number & Descriptions

A. General Product Information
Ignitability characteristic: use EPA hazardous waste number D001 (waste code I)

Disposal Instructions:
All waste must be handled in accordance with local, state and federal regulations.
# Puncture containers to prevent re-use and bury at an authorized landfill.
Explosives which are surplus, deteriorated or considered unsafe for transport, storage or use shall be destroyed and the statutory authorities shall be notified.
Explosives must not be thrown away, buried, discarded or placed with garbage.
This material may be disposed of by burning or detonation but the operation must be performed under the control of a person competent in the destruction of explosives.

Disposal by detonation:
The explosives to be destroyed must be placed in direct contact with fresh priming charge in a hole which is at least 0.6 meter deep and then adequately stemmed.
No detonators shall be inserted into defective explosives.
Personnel must be evacuated to a safe distance prior to initiation/firing of the charge. Disposal by burning:
Make a sawdust bed or trail adequate for the quantity of explosives to be burned, approximately 400mm wide and 40 mm deep, upon which the explosive will be laid.
If sawdust is not available, newspaper may be used.
Normal precautions shall be taken to avoid the spread of fire.
Individual trails should not be closer together than 600 mm and should contain not more than 12 Kg of explosive.
Trails should be side by side, NOT in-line, and not more than four should be set up at one time.
Remove any explosive that is not to be burnt to a distance of at least 300 meter.
Sufficient diesel oil (never petrol or other highly inflammable liquid) should be used to thoroughly wet the sawdust (or paper) at least 4L per trail is recommended.
Light the trail from a long, rolled paper wick which should be placed downwind and in contact with the end 1m of trail that is not covered with explosive. The wind should blow so that the flame from the wick (and later from the burning explosive) will blow away from the unburned explosive as detonation is more likely to occur if the explosive is preheated by the flame.
If plastic igniter cord (slow) is available, its use for lighting is recommended instead of paper. One end should be coiled into the sawdust or under the paper and the other end lit from a minimum distance of 7m from the trail.
Retire at least 300m or to a safe place.
DO NOT return to the site for at least 30 minutes after the burning has apparently finished.
If the fire goes out do not approach for at least 15 minutes after all trace of fire has gone.
DO NOT add more diesel oil unless certain that the flame is completely extinguished.


Symbols: None
Hazard class or Division: 4.1
Identification Numbers: UN1344 PG: I
Label Codes: 4.1 Special provisions: 23, A8, A19, N41
Packaging: Exceptions: None Packaging: Non-bulk: 211
Packaging: Exceptions: None
Quantity limitations: Passenger aircraft/rail: 1 kg
Quantity Limitations: Cargo aircraft only: 15 kg Vessel stowage: Location: E
Vessel stowage: Other: 28, 36
Hazardous materials descriptions and proper shipping names: Trinitrophenol, wetted or Picric acid, wetted, with not less than 30 percent water by mass
Air Transport IATA:
ICAO/IATA Class: 4.1 ICAO/IATA Subrisk: !$
UN/ID Number: 1344 Packing Group: I
Special provisions: A40
Maritime Transport IMDG:
IMDG Class: 4.1 IMDG Subrisk: None
UN Number: 1344 Packing Group: I
EMS Number: F-B,S-J Special provisions: 28
Limited Quantities: None
Shipping Name: TRINITROPHENOL, WETTED with not less than 30% water, by mass


SARA Section 302 Extremely Hazardous Substances: No chemicals in this product have a TPQ.
SARA Codes: CAS # 88-89-1: immediate, delayed, fire, sudden release of pressure, reactive.
Section 313: This material contains Picric acid (CAS# 88-89-1, <70%),which is subject to the reporting requirements of Section 313 of SARA Title III and 40 CFR Part 373.
California Prop 65: None of the chemicals in this product are listed.

Canada - DSL/NDSL: CAS# 88-89-1 is listed on Canada's DSL List.
Canada - WHMIS: This product has a WHMIS classification of B4, D1B, D2B, E.
Canadian Ingredient Disclosure List: AS# 88-89-1 is listed.


EINECS EC Number: 201-865-9
European Labeling in Accordance with EC Directives
H201 Explosive; mass explosion hazard
H228: Flammable solid
H241: Heating may cause a fire or explosion.
H301: Toxic if swallowed.
H311: Toxic in contact with skin.
H319 Causes serious eye irritation.
H331: Toxic if inhaled.

Hazard Symbols: T F
Risk Phrases: R 1 Explosive when dry. R 11 Highly flammable. R 23/24/25 Toxic by inhalation, in contact with skin and if swallowed. R 4 Forms very sensitive explosive metallic compounds. R 43 May cause sensitization by skin contact.

Our company provides this MSDS sheet in good faith but makes no representation as to its comprehensiveness or accuracy. This SDS sheet is intended only as a guide to the appropriate precautionary handling of the material by a properly trained person using this product. The above information has been compiled from various sources and has the possibility of discrepancy and being out-dated information. Individuals receiving the information must exercise their independent judgment and do further search in determining its appropriateness for a particular purpose. In no case shall our company be liable to loss or damages by the product user.



Taloja Mumbai and Ankleshwar Gujarat, INDIA
Representatives in Houston, Chicago and New York, USA
TEL: (OFF) 91-22-23726950, 23774610, 23723564


Copyright and Usual Disclaimer is Applicable
Last updated 15-jan-19

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Picric Acid
Picric acid