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Tolylene-2,4-diisocyanate

Tolylene-2,4-diisocyanate Structure
CAS No.
584-84-9
Chemical Name:
Tolylene-2,4-diisocyanate
Synonyms
TDI;TDI-80;2,4-TDI;2,4-TOLUENEDIISOCYANATE;Scuranate;SCURANATE TX;Desmodur T80;Nacconate 100;TOLUENE-2,4-DIISOCYANATE;Tolylene-2,4-diisocyanate 95%
CBNumber:
CB6170855
Molecular Formula:
C9H6N2O2
Molecular Weight:
174.16
MOL File:
584-84-9.mol
MSDS File:
SDS
Modify Date:
2024/4/29 9:50:43

Tolylene-2,4-diisocyanate Properties

Melting point 20-22 °C(lit.)
Boiling point 124-126 °C18 mm Hg(lit.)
Density 1.225 g/mL at 25 °C
vapor density 6 (vs air)
vapor pressure 0.03 mm Hg ( 25 °C)
refractive index n20/D 1.568(lit.)
Flash point 250 °F
storage temp. 2-8°C
solubility Miscible with ether, acetone, benzene, carbontetrachloride and chlorobenzene.
form Liquid
color Colorless
Specific Gravity 1.225
Odor Sharp, pungent odor detectable at 0.02 to 0.4 ppm
explosive limit 9.5%
Water Solubility reacts
Sensitive Moisture Sensitive
Merck 14,9530
BRN 744602
Exposure limits TLV-TWA 0.0355 mg/m3 (0.005 ppm) (ACGIH and NIOSH); STEL or ceiling/10 min 0.142 mg/m3 (0.02 ppm) (ACGIH, NIOSH, and OSHA); IDLH 71 mg/m3 (10 ppm) (NIOSH).
Stability Stable, but decomposes in the presence of moisture. Also heat and light sensitive. Readily polymerizes in contact with base. Reacts with compounds containing active hydrogen. Incompatible with strong oxidizing agents. Corrodes some copper and aluminium alloys.
InChIKey DVKJHBMWWAPEIU-UHFFFAOYSA-N
LogP 3.43 at 22℃
CAS DataBase Reference 584-84-9(CAS DataBase Reference)
NIST Chemistry Reference Benzene, 2,4-diisocyanato-1-methyl-(584-84-9)
EPA Substance Registry System Toluene-2,4-diisocyanate (584-84-9)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06,GHS08
Signal word  Danger
Hazard statements  H315-H317-H319-H330-H334-H335-H351-H412
Precautionary statements  P202-P273-P280-P302+P352-P304+P340+P310-P305+P351+P338
Hazard Codes  T+
Risk Statements  26-36/37/38-40-42/43-52/53
Safety Statements  23-36/37-45-61
RIDADR  UN 2078 6.1/PG 2
WGK Germany  2
RTECS  CZ6300000
10-21
Autoignition Temperature >619 °C
TSCA  Yes
HazardClass  6.1
PackingGroup  II
HS Code  29291010
Toxicity Acute oral LD50 for rats 5,800 mg/kg, wild birds 100 mg/kg (quoted, RTECS, 1985).
IDLA 2.5 ppm
NFPA 704
1
3 2

Tolylene-2,4-diisocyanate price More Price(12)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) T39853 Tolylene-2,4-diisocyanate 95% 584-84-9 100G ₹6614.08 2022-06-14 Buy
Sigma-Aldrich(India) T39853 Tolylene-2,4-diisocyanate 95% 584-84-9 250G ₹8768.25 2022-06-14 Buy
Sigma-Aldrich(India) 89870 Toluene 2,4-diisocyanate purum, suitable for electron microscopy, ≥98.0% (GC) 584-84-9 100ML ₹12676.08 2022-06-14 Buy
Sigma-Aldrich(India) 89870 Toluene 2,4-diisocyanate purum, suitable for electron microscopy, ≥98.0% (GC) 584-84-9 500ML ₹36252.93 2022-06-14 Buy
Sigma-Aldrich(India) 33427 2,4-TDI analytical standard 584-84-9 5ML ₹8356.9 2022-06-14 Buy
Product number Packaging Price Buy
T39853 100G ₹6614.08 Buy
T39853 250G ₹8768.25 Buy
89870 100ML ₹12676.08 Buy
89870 500ML ₹36252.93 Buy
33427 5ML ₹8356.9 Buy

Tolylene-2,4-diisocyanate Chemical Properties,Uses,Production

Description

Toluene diisocyanate (TDI), (OCN)2C6H3CH3, is a water-white to pale-yellow liquid with a sharp, pungent odor. It reacts with water to release carbon dioxide. The specific gravity is 1.22, which is heavier than water. TDI is toxic by inhalation and ingestion, and is a strong irritant to skin and other tissue, particularly the eyes. The TLV is 0.005 ppm in air, and the IDLH is 10 ppm. The target organs are the respiratory system and the skin. The four-digit UN identification number is 2078. The NFPA 704 designation is health 3, flammability 1, and reactivity 3. The white section at the bottom of the diamond has a W with a slash through it, indicating water reactivity. The primary uses of TDI are in the manufacture of polyurethane foams, elastomers, and coatings.

Chemical Properties

colourless to light yellow liquid

Physical properties

Clear, colorless to light yellow liquid with a pungent, fruity odor. Odor threshold concentration in air is 2.14 ppmv (Leonardos et al., 1969).

Uses

Occupational asthma is the principal cause of work-related respiratory disease in the industrial world. Toluene-2,4-diisocyanate (TDI) is one of the most common respiratory sensitizers leading to occupational asthma.

Definition

ChEBI: A toluene meta-diisocyanate in which the isocyanato groups are at positions 2 and 4 relative to the methyl group on the benzene ring.

General Description

2,4-TDI is an environmental contaminant belonging to the class of diisocyanates. It is commercially used as a starting material for varnishes, paints, elastomers, polyurethane foams, wire enamels, etc.

Air & Water Reactions

Reacts with water with the evolution of carbon dioxide and formation of insoluble polyureas that are relatively nontoxic and inert [Merck 11th ed. 1989)].

Reactivity Profile

Tolylene-2,4-diisocyanate is explosive in the form of vapor when exposed to heat, flame or sparks. Undergoes potentially violent polymerization reaction with strong bases or acyl chlorides. Reacts with water to liberate carbon dioxide. Potential explosion if stored in polyethylene containers due to absorption of water through the plastic. Emits very toxic fumes of oxides of nitrogen when heated to decomposition [Lewis, 3rd ed., 1993, p. 1251].

Hazard

Toxic by ingestion and inhalation; strong irritant to skin and tissue, especially to eyes. Respiratory sensitization.

Health Hazard

Can cause death. Contact with skin may cause allergic eczema. Substance is very corrosive to eyes. Chronic exposure may cause chronic lung disease. As a vapor TDI is a powerful irritant to the respiratory tract. Chronic loss of respiratory function may occur. Acute asthmatic bronchitis or frank asthma may occur. A splash in the eyes of workmen has caused keratitis and conjunctivitis. Tolylene-2,4-diisocyanate causes inflammation of the skin, also chemical pneumonitis and pulmonary edema.

Fire Hazard

When heated to decomposition Tolylene-2,4-diisocyanate emits very toxic fumes of cyanide and nitrogen oxides. Reacts violently with amines, alcohol, bases and warm water causing fire and explosion hazards. Avoid strong oxidizers, water, acids, bases, amines, etc., cause foam and splatter. Avoid heating. Hazardous polymerization may occur. Concentrated alkaline compound such as sodium hydroxide or tertiary amines may cause run-away polymerization. Slow, not hazardous polymerization may occur above 235F.

Flammability and Explosibility

TDI is a combustible liquid (NFPA rating = 1). Explosive limits in air are 0.9 to 9.5% by volume. Carbon dioxide or dry chemical extinguishers should be used for TDI fires.

Chemical Reactivity

Reactivity with Water: A non violent reaction occurs forming carbon dioxide gas and an organic base; Reactivity with Common Materials: No reactions; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Slow polymerization occurs at temperatures above 113°F. The reaction is not hazardous; Inhibitor of Polymerization: Not pertinent.

Safety Profile

Confirmed carcinogen. Poison by ingestion, inhalation, and intravenous routes. Human systemic effects by inhalation: unspecified changes to the eyes and sense of smell, respiratory obstruction, cough, sputum, and other pulmonary and gastrointestinal changes. Mutation data reported. A severe skin and eye irritant. Capable of producing severe dermatitis and bronchial spasm. A common air contaminant. Combustible when exposed to heat or flame. Explosive in the form of vapor when exposed to heat or flame. To fight fire, use dry chemical, CO2. Potentially violent polymerization reaction with bases or acyl chlorides. Reaction with water releases carbon dioxide. Storage in polyethylene containers is hazardous due to absorption of water through the plastic. When heated to decomposition it emits highly toxic fumes of NOx. See also ISOCYANATES.

Carcinogenicity

Acute toxicity. Industrial experience has demonstrated that acute exposure to TDI vapors can produce severe irritant effects on mucous membranes, the respiratory tract, and the eyes. An acute attack of an asthma-like syndrome may occur. Exposure to high concentrations may lead to chemical bronchitis with severe bronchospasm, chemical pneumonitis, pulmonary edema, headache, and insomnia.With sufficient exposure, all persons would appear to experience these effects even on their first exposure.
Chronic and subchronic toxicity. Repeated exposures at lower concentrations of TDI may produce a chronic-like syndrome in many people. Symptoms may include coughing, wheezing, tightness or congestion in the chest, and shortness of breath and appear to be related to hypersensitization. Interstitial pulmonary fibrosis does not occur from moderately elevated exposures to TDI (mean 0.07, peak 0.2 ppm).
Exposure to TDI may lead to immunological sensitization. Some individuals become sensitized on first exposure; others may develop symptoms after exposure over days, months, or years. Other workers have experienced only minimal or no respiratory symptoms for several months of low level exposure, then suddenly develop acute asthmatic reactions to the same level. The nature of the sensitization process is unknown, and many authors have referred to it as an “allergy;” the respiratory response in sensitized people is referred to as true asthma, comparable to asthma excited by pollens and other exoallergens. Some TDI-sensitized people, however, have no history of prior allergic disease.

Environmental Fate

Chemical/Physical. Slowly reacts with water forming carbon dioxide and polyureas (NIOSH, 1997; Windholz et al., 1983).

storage

work with TDI should be conducted in a fume hood to prevent exposure by inhalation, and splash goggles and impermeable gloves should be worn at all times to prevent eye and skin contact.

Purification Methods

It is purified by fractionation in a vacuum and should be stored in a dry atmosphere. It is soluble in organic solvents but reacts with H2O, alcohols (slowly) and amines, all of which could cause explosive polymerisation. It darkens on exposure to light. It has a sharp pungent odour, is TOXIC and is IRRITATING TO THE EYES. [Siefken Justus Liebigs Ann Chem 562 75, 96, 127 1949, Bayer Angew Chem 59 257 1947.] It is a reagent for covalent crosslinking of proteins [Wold Methods Enzymol 25 623 1972.] [Beilstein 13 IV 243.]

Incompatibilities

Contact with strong oxidizers may cause fires and explosions. Contact with water, acids, bases, and amines can lead to reactions that liberate heat and CO2 and cause violent foaming and spattering. TDI will attack some forms of plastic, rubber, and coatings.

Waste Disposal

Excess TDI and waste material containing this substance should be placed in an appropriate container, clearly labeled, and handled according to your institution's waste disposal guidelines.

Precautions

Occupational workers should be careful during use and waste disposal of toluene diisocyanate. Use and storage of toluene diisocyanate requires precautions. It polymerizes under the infl uence of bases, tertiary amines, and acyl chlorides with fi re or explosion hazard. On combustion, it forms toxic vapors and gases, including nitrogen oxides and isocyanates. Toluene diisocyanate reacts readily with water, acids, and alcohols, and causes explosion hazard. The development of any unusual signs or symptoms, such as headache, increased pain or a discharge from the eyes, increased redness or pain or a pus-like discharge in the area of a skin burn within 24 h after exposure to toluene diisocyanate, requires immediate medical support to the exposed worker.

Global( 260)Suppliers
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