PRODUCTS

P-ISOPROPYLPHENYL ISOCYANATE

p-isopropylphenyl isocyanate is used pharmaceutical/medicinal-chemistry research, Specialty polymer/coating research.
p-isopropylphenyl isocyanate is a reactive aromatic monoisocyanate used primarily as an intermediate in agrochemical production, particularly in phenylurea/herbicide chemistry, and as a building block for urea, carbamate and other specialty organic compounds.

CAS Number: 31027-31-3
EC Number / EINECS: 250-439-9
Molecular Formula: C10H11NO
Molecular Weight: 161.20 g/mol (161.204 g/mol)

SYNONYMS:
4-Isopropylphenyl isocyanate, p-Isopropylphenyl isocyanate, p-Isopropyl phenyl isocyanate, 1-Isocyanato-4-isopropylbenzene, 1-Isocyanato-4-(propan-2-yl)benzene, 1-Isocyanato-4-(1-methylethyl)benzene, Benzene, 1-isocyanato-4-(1-methylethyl)-, p-Cumenyl isocyanate, 4-Isocyanatocumene, p-Isocyanatocumene, Isocyanic acid (4-isopropylphenyl ester), Isocyanic acid (p-isopropylphenyl ester), p-Isopropyl-isocyanatobenzene, 4-Isopropylphenylcarbimide, p-Isopropylphenylcarbimide, 4-Isopropylphenylisocyanat, 4-Isopropylphenylisocyanate, p-Isopropylphenylisocyanat, IPPI, p-IPI, AKOS B028613, ART-CHEM-BB B028613,4-isopropylphenyl isocyanate, 4-isopropylphenylisocyanate, 1-isocyanato-4-isopropylbenzene, 1-isocyanato-4-isopropyl-benzene, p-isopropylphenyl isocyanate, benzene, 1-isocyanato-4-1-methylethyl, 4-isopropyl phenylisocyanate, 4-methylethyl benzenisocyanate, p-cumenyl isocyanate, acmc-1aild,1-isocyanato-4-isopropylbenzene,p-Isopropylphenyl isocyanate,1-Isocyanato-4-(propan-2-yl)benzene,Benzene, 1-isocyanato-4-(1-methylethyl)-,31027-31-3,EINECS 250-439-9,1-isocyanato-4-(propan-2-yl)benzene,IPPI,AKOS B028613,ART-CHEM-BB B028613,p-cumenylisocyanate,4-Isopropylphenyl is,p-Isopropylphenylisocyanat,4-Isopropylphenylisocyanat,4-ISOPROPYLPHENYL ISOCYANATE,P-ISOPROPYL PHENYL ISOCYANATE

p-isopropylphenyl isocyanate is an aromatic monoisocyanate consisting of a benzene ring carrying an isocyanate group and an isopropyl group in the para (4-) position.
p-isopropylphenyl isocyanate therefore combines two important structural features: a relatively hydrophobic aromatic/isopropyl portion and a highly reactive isocyanate group (-N=C=O).

The isocyanate group is the chemically active part of p-isopropylphenyl isocyanate.
p-isopropylphenyl isocyanate reacts readily with compounds containing nucleophilic functional groups, particularly alcohols and amines, which makes aromatic isocyanates valuable intermediates for preparing urethanes, ureas, carbamates and related compounds.

Commercial information specifically identifies p-isopropylphenyl isocyanate as an intermediate for agrochemical production, including pesticide and herbicide production, and for advanced organic and fine-chemical synthesis
p-isopropylphenyl isocyanate is a clear, colorless to yellow or orange liquid

p-isopropylphenyl isocyanate, also known as 4-isopropylphenyl isocyanate, 4-isocyanatocumene, p-isocyanatocumene, or IPPI, is a para-substituted aromatic monoisocyanate with CAS No. 31027-31-3, EC No. 250-439-9, molecular formula C10H11NO, and molecular weight 161.20 g/mol.
Structurally, p-isopropylphenyl isocyanate consists of a benzene ring carrying an isopropyl group (-CH(CH3)2) and an isocyanate group (-N=C=O) in the para position.

The isopropyl group gives p-isopropylphenyl isocyanate a relatively hydrophobic aromatic character, whereas the isocyanate group provides its principal chemical reactivity.
This combination makes p-isopropylphenyl isocyanate much more useful as a reactive building block than as a final-use chemical.

p-isopropylphenyl isocyanate's principal commercial importance is as an intermediate for agrochemicals, particularly pesticide and herbicide synthesis, as well as for advanced organic and fine-chemical synthesis.
p-isopropylphenyl isocyanate can be viewed as a specialty chemical building block that transfers a 4-isopropylphenyl group into more complex urea or carbamate molecules.

USES and APPLICATIONS of P-ISOPROPYLPHENYL ISOCYANATE:
Primary established application of p-isopropylphenyl isocyanate: Agrochemical intermediate.
Major specific application of p-isopropylphenyl isocyanate: Intermediate for isoproturon and related phenylurea chemistry.
Other established application of p-isopropylphenyl isocyanate: Pesticide and herbicide intermediate production.

Synthetic application: Preparation of substituted ureas, Preparation of carbamates
Specialty-chemical application of p-isopropylphenyl isocyanate: Advanced organic and fine-chemical synthesis.
Research application of p-isopropylphenyl isocyanate: Preparation of complex aromatic urea/carbamate molecules.

-Isoproturon Production uses of p-isopropylphenyl isocyanate:
The connection with isoproturon deserves particular emphasis.
Isoproturon is a phenylurea herbicide, and its structure can be obtained by reacting 4-isopropylphenyl isocyanate with dimethylamine.

p-isopropylphenyl isocyanate is the precursor in this manufacturing route.
This means that p-isopropylphenyl isocyanate serves as the aryl-isocyanate precursor that supplies the 4-isopropylphenyl portion of the final phenylurea molecule.
This is probably the most useful specific example to mention when describing the industrial significance of CAS 31027-31-3.

-Carbamate Synthesis uses of p-isopropylphenyl isocyanate:
Another important application of p-isopropylphenyl isocyanate is the preparation of carbamates.
When the isocyanate group reacts with an alcohol:
Ar-NCO + R-OH → Ar-NH-CO-OR the product is a carbamate.

p-isopropylphenyl isocyanate is an intermediate for urea and carbamate synthesis.
Carbamates are important structural classes used in: Agrochemical chemistry, Pharmaceutical chemistry, Fine chemicals, Specialty organic synthesis.
Therefore, p-isopropylphenyl isocyanate has synthetic utility beyond its documented herbicide-related application.

-Advanced Organic Synthesis uses of p-isopropylphenyl isocyanate:
In advanced organic and fine-chemical synthesis, p-isopropylphenyl isocyanate is used as an application area.
In this context, p-isopropylphenyl isocyanate can be used as a controlled reagent for introducing a 4-isopropylphenyl-derived urea or carbamate functionality into a target molecule.

This makes p-isopropylphenyl isocyanate potentially useful during: Route development, Intermediate synthesis, Structure optimization, Medicinal-chemistry research, Agrochemical research, Specialty chemical development.
However, these should be understood as synthetic/research applications, rather than implying that p-isopropylphenyl isocyanate itself is an approved pharmaceutical or pesticide.

-Pharmaceutical And Medicinal Chemistry Research uses of p-isopropylphenyl isocyanate:
p-isopropylphenyl isocyanate can also serve as a building block in medicinal chemistry because aryl ureas and carbamates are common structural motifs in bioactive molecules.
A search of chemical literature and supplier information shows examples where p-isopropylphenyl isocyanate participates in the synthesis of more complex biologically active molecules.

For example, chemical databases document p-isopropylphenyl isocyanate's use as a reactant in the synthesis of substituted urea structures investigated for biological activity.
This does not mean that p-isopropylphenyl isocyanate itself is a pharmaceutical active ingredient.
p-isopropylphenyl isocyanate's role is that of a synthetic precursor/reagent.

-Fine-Chemical Manufacturing uses of p-isopropylphenyl isocyanate:
Because p-isopropylphenyl isocyanate is available commercially at high purity, it can be used in specialty and fine-chemical manufacturing.
Commercial suppliers offer material at approximately 98% purity, and p-isopropylphenyl isocyanate is a specialty intermediate suitable for advanced synthesis.
p-isopropylphenyl isocyanate's commercial value therefore comes from its ability to provide a relatively well-defined and reactive building block rather than from bulk-volume applications.

-Research And Development uses of p-isopropylphenyl isocyanate:
p-isopropylphenyl isocyanate is also relevant to laboratory-scale research and development.
p-isopropylphenyl isocyanate can be used when researchers need to prepare: N-substituted ureas, Aryl carbamates, Phenylurea analogues, Specialty organic intermediates, Structure–activity relationship compounds, Agrochemical candidates, Fine-chemical intermediates.
The availability of a defined CAS-numbered material makes p-isopropylphenyl isocyanate particularly useful for reproducible synthetic work.

-Potential Materials-Chemistry Applications of p-isopropylphenyl isocyanate:
Isocyanates are important reagents in polymer and coating chemistry.
Consequently, p-isopropylphenyl isocyanate can be investigated as a specialty monoisocyanate in research involving polyurethane or related materials.
However, this is a much less clearly documented application for this particular compound than p-isopropylphenyl isocyanate's agrochemical-intermediate role.

Therefore, p-isopropylphenyl isocyanate is better to describe polymer/coating use as a potential or research application, rather than as a major established commercial use of CAS 31027-31-3.
One commercial technical source similarly describes material-science applications as an area in which p-isopropylphenyl isocyanate can be investigated.

-Herbicide Intermediate uses of p-isopropylphenyl isocyanate:
The most specifically documented application is p-isopropylphenyl isocyanate's use as an intermediate for herbicides.
In particular, p-isopropylphenyl isocyanate is a precursor to isoproturon, a phenylurea herbicide.

The preparation of isoproturon by reacting 4-isopropylphenyl isocyanate with dimethylamine.
The simplified reaction is:
4-Isopropylphenyl isocyanate + dimethylamine → isoproturon

The resulting molecule contains the characteristic phenylurea structure.
This is an important example because it demonstrates that p-isopropylphenyl isocyanate is not merely a theoretical laboratory reagent; it has a documented role in the synthesis of a commercially important agricultural chemical.

-Pesticide Intermediate uses of p-isopropylphenyl isocyanate:
Beyond the specific isoproturon example, p-isopropylphenyl isocyanate more broadly as an intermediate used in pesticide production.
p-isopropylphenyl isocyanate's value in pesticide chemistry comes from its ability to introduce the 4-isopropylphenyl group together with an isocyanate-derived carbonyl/urea functionality.

This makes p-isopropylphenyl isocyanate useful for constructing molecules whose final structures contain: A substituted phenyl ring, A urea linkage, A carbamate linkage or related nitrogen-containing carbonyl structures.
Therefore, p-isopropylphenyl isocyanate is best classified as an agrochemical synthesis intermediate, rather than as an agrochemical active ingredient itself.

-Phenylurea Synthesis uses of p-isopropylphenyl isocyanate:
One of p-isopropylphenyl isocyanate's most important chemical applications is the preparation of phenylurea derivatives.
p-isopropylphenyl isocyanate reacts with a primary or secondary amine to generate a substituted urea.

For example:
Ar-NCO + RNH2 → Ar-NH-CO-NHR
where:
Ar = 4-isopropylphenyl

This type of transformation is extremely useful because phenylureas constitute an important class of compounds in agricultural chemistry.
The 4-isopropyl substituent can influence the physical and biological properties of the resulting molecule, while the urea group provides a second important functional component.

-Agrochemical intermediate uses of p-isopropylphenyl isocyanate:
The most clearly documented industrial application is its use as an intermediate in agrochemical production.
p-isopropylphenyl isocyanate is a key intermediate for crop-protection chemistry, including pesticide and herbicide production.

The isocyanate group allows p-isopropylphenyl isocyanate to be incorporated into more complex molecules through reactions with amines, alcohols and other nucleophiles.
Therefore, p-isopropylphenyl isocyanate's role is generally that of a chemical building block, rather than the final active ingredient itself.

-Pesticide And Herbicide Synthesis uses of p-isopropylphenyl isocyanate:
p-isopropylphenyl isocyanate is relevant to the synthesis of certain pesticide and herbicide intermediates.
This application is based on the ability of aryl isocyanates to produce substituted urea and carbamate structures.

The resulting molecules can possess very different biological and physicochemical properties from the original isocyanate.
It is therefore more accurate to describe p-isopropylphenyl isocyanate as a synthetic intermediate used in crop-protection chemistry, rather than as a pesticide itself.

-Urea Synthesis uses of p-isopropylphenyl isocyanate:
A major synthetic application of aromatic isocyanates is the preparation of aryl ureas.
Reaction with an appropriate amine produces an N-substituted urea derivative.
This is chemically useful because substituted aromatic ureas occur in many areas of medicinal chemistry, agrochemistry and specialty organic synthesis.
The para-isopropyl substituent provides a hydrophobic aromatic substituent that can be retained in the final molecule.

-Carbamate Synthesis uses of p-isopropylphenyl isocyanate:
Reaction of p-isopropylphenyl isocyanate with an alcohol or phenol can produce a corresponding carbamate.
Carbamates are important structural motifs in: Agrochemicals, Pharmaceutical intermediates, Specialty chemicals, Organic synthesis
p-isopropylphenyl isocyanate therefore functions as a convenient source of the –NH–CO– portion of a carbamate structure.

-Fine Chemical Synthesis uses of p-isopropylphenyl isocyanate:
p-isopropylphenyl isocyanate is also used as an intermediate in advanced organic and fine-chemical synthesis.
This is particularly relevant where a para-isopropylphenyl group needs to be introduced into a target molecule through an isocyanate reaction.

-Research And Laboratory Use of p-isopropylphenyl isocyanate:
Commercial suppliers offer p-isopropylphenyl isocyanate in high-purity grades, including approximately 98% material, primarily for research and synthetic applications.
p-isopropylphenyl isocyanate is therefore used as a laboratory reagent and synthetic building block for preparing more complex organic molecules.

BENEFITS AND TECHNICAL ADVANTAGES of P-ISOPROPYLPHENYL ISOCYANATE:
The principal benefits of p-isopropylphenyl isocyanate are synthetic rather than consumer-oriented.
Its main advantages include:

High chemical reactivity:
The isocyanate group readily reacts with suitable nucleophiles.

Useful aromatic substituent:
The para-isopropylphenyl group can be incorporated into larger molecules.

Versatile intermediate:
p-isopropylphenyl isocyanate can participate in both urea and carbamate synthesis.

Agrochemical relevance:
p-isopropylphenyl isocyanate is useful in crop-protection intermediate synthesis.

Fine-chemical versatility:
p-isopropylphenyl isocyanate can be used as a building block in advanced organic synthesis.

Commercial availability:
High-purity grades are commercially available.

Defined molecular structure:
p-isopropylphenyl isocyanate is a single, well-defined aromatic monoisocyanate rather than a polymeric mixture.

Good organic-phase compatibility:
p-isopropylphenyl isocyanate's Log P of approximately 4.05 reflects appreciable lipophilicity.

MOLECULAR STRUCTURE of P-ISOPROPYLPHENYL ISOCYANATE:
The molecule of p-isopropylphenyl isocyanate consists of:
One benzene ring
One isopropyl group, –CH(CH3)2
One isocyanate group, –N=C=O
The isopropyl group and isocyanate group occupy the para positions on the aromatic ring.
A simplified structural representation is: p-(CH(CH3)2)–C6H4–N=C=O
The molecular formula is C10H11NO.
The molecule contains:
10 carbon atoms
11 hydrogen atoms
1 nitrogen atom
1 oxygen atom
1 aromatic ring
1 isocyanate functional group
The isocyanate functionality is responsible for most of p-isopropylphenyl isocyanate's chemical reactivity.

INDUSTRIAL IMPORTANCE of P-ISOPROPYLPHENYL ISOCYANATE:
The industrial importance of p-isopropylphenyl isocyanate comes from three main characteristics.
First, p-isopropylphenyl isocyanate contains a highly reactive isocyanate group.
Second, p-isopropylphenyl isocyanate contains a 4-isopropylphenyl structural unit that can be retained in the final molecule.

Third, p-isopropylphenyl isocyanate is a relatively small, well-defined molecule that can be used as a single-step building block for more complex compounds.
This makes p-isopropylphenyl isocyanate particularly convenient for producing molecules in which the desired structure contains both an aromatic hydrophobic substituent and a urea/carbamate functionality.

WHY THE PARA-ISOPROPYL GROUP MATTERS:
The isopropyl group is not merely a passive substituent.
It increases the hydrophobic character of the aromatic ring and changes the steric and electronic environment around the phenyl group.
The para arrangement gives a relatively symmetrical substituted aromatic structure:
p-Isopropylphenyl–NCO
This structure can be incorporated into target molecules while maintaining the 4-isopropylphenyl motif.
In the case of isoproturon, this structural element is retained in the final herbicide molecule.

CHEMICAL PROPERTIES of P-ISOPROPYLPHENYL ISOCYANATE:
The most important chemical property of p-isopropylphenyl isocyanate is its isocyanate functional group.
The general isocyanate structure is: R–N=C=O
In p-isopropylphenyl isocyanate: R = p-isopropylphenyl
The carbon atom of the isocyanate group is strongly electrophilic.

Consequently, p-isopropylphenyl isocyanate reacts with nucleophilic substances such as:
Primary amines
Secondary amines
Alcohols
Phenols
Water
and other compounds containing suitable nucleophilic functional groups.

Reaction with an alcohol can form a urethane/carbamate, while reaction with an amine can form a urea derivative.
Because water contains nucleophilic hydroxyl functionality, moisture can consume the isocyanate group and lead to hydrolysis/reaction products.
This explains why p-isopropylphenyl isocyanate is specifically described as moisture sensitive.

REACTIVITY of P-ISOPROPYLPHENYL ISOCYANATE:
p-isopropylphenyl isocyanate is a reactive organic intermediate.
The –N=C=O group is substantially more reactive than the hydrocarbon portion of the molecule.
p-isopropylphenyl isocyanate's important reactions include:

Reaction with amines: formation of substituted ureas.
Reaction with alcohols: formation of carbamates/urethanes.
Reaction with phenols: formation of aryl carbamates.

Reaction with water: hydrolysis and subsequent formation of reaction products.
Reaction with other nucleophiles: formation of corresponding substituted isocyanate-addition products.
This reactivity is the principal reason p-isopropylphenyl isocyanate is useful in synthetic chemistry.

CHARACTERISTICS of P-ISOPROPYLPHENYL ISOCYANATE:
p-isopropylphenyl isocyanate can be characterized as a:
Aromatic monoisocyanate
Para-substituted phenyl isocyanate

Reactive organic intermediate
Electrophilic chemical intermediate
Moisture-sensitive compound

Hydrophobic organic compound
Moderately lipophilic substance
Low-molecular-weight aromatic chemical

Liquid at room temperature
Specialty chemical intermediate
Agrochemical intermediate

Fine-chemical synthesis intermediate
Urea-forming reagent

Carbamate-forming reagent
p-isopropylphenyl isocyanate's combination of an aromatic ring, isopropyl substituent and reactive isocyanate group gives it a useful balance between organic-solvent compatibility and synthetic reactivity.

CHEMICAL BEHAVIOUR IN SYNTHESIS of P-ISOPROPYLPHENYL ISOCYANATE:
One particularly useful feature of p-isopropylphenyl isocyanate is that it can act as a one-step electrophilic building block.
For example, conceptually:
p-isopropylphenyl isocyanate + amine → substituted aryl urea and:
p-isopropylphenyl isocyanate + alcohol → substituted aryl carbamate

This makes p-isopropylphenyl isocyanate useful when a synthetic route requires simultaneous introduction of:
A para-isopropylphenyl group and A urea/carbamate carbonyl-containing functionality.
Its usefulness therefore comes primarily from p-isopropylphenyl isocyanate's reactive isocyanate functionality, rather than from any physical property such as volatility or solubility.

WHY THE ISOCYANATE GROUP IS IMPORTANT
The central feature of p-isopropylphenyl isocyanate is the -N=C=O functional group.
Isocyanates are highly reactive electrophilic compounds.
The carbon atom in the isocyanate group is particularly susceptible to nucleophilic attack.

Consequently, p-isopropylphenyl isocyanate can react with compounds containing functional groups such as:
Amines
Alcohols
Phenols
Water
and other nucleophilic reagents.
This gives p-isopropylphenyl isocyanate considerable synthetic versatility.
The general reactions can be represented conceptually as:
p-isopropylphenyl isocyanate + amine → substituted phenyl urea
and:

p-isopropylphenyl isocyanate + alcohol → substituted carbamate
The ability to form these two important classes of compounds explains much of p-isopropylphenyl isocyanate's value in agrochemical and specialty-chemical synthesis.

PHYSICAL and CHEMICAL PROPERTIES of P-ISOPROPYLPHENYL ISOCYANATE:
Chemical Name: p-Isopropylphenyl isocyanate
Preferred/Common Name: 4-Isopropylphenyl isocyanate
IUPAC Name: 1-Isocyanato-4-(propan-2-yl)benzene
CAS Number: 31027-31-3
EC Number / EINECS: 250-439-9
Molecular Formula: C10H11NO
Molecular Weight: 161.20 g/mol (161.204 g/mol)
PubChem CID: 9441
MDL Number: MFCD00013880

Beilstein/BRN: 2936403
InChIKey: PJVRNNRZWASOIT-UHFFFAOYSA-N
SMILES: CC(C)C1=CC=C(C=C1)N=C=O
Chemical class: Aromatic isocyanat
Functional group: Isocyanate, –N=C=O
Physical form: Liquid at approximately 20 °C
General chemical character: Reactive, moisture-sensitive, aromatic monoisocyanate.
Appearance: Clear, colorless to yellow/orange or light-brown liquid, depending on purity and supplier description.

Physical state at 20 °C: Liquid.
Molecular weight: 161.20–161.21 g/mol.
Molecular formula: C10H11NO.
Density: Approximately 1.01 g/mL at 25 °C.
Boiling point: Approximately 85 °C at 4 mmHg.
Flash point: Approximately 90–94 °C depending on the source and measurement method.
Refractive index: Approximately n20/D = 1.52, with one supplier reporting approximately 1.5190–1.5210.
Water solubility: The substance is reported to decompose in water, rather than behaving as a stable, freely water-soluble compound.
Moisture sensitivity: Moisture sensitive.

Log P: Approximately 4.05 at 20 °C, indicating significant lipophilicity.
Vapour characteristics: Because it is a relatively low-molecular-weight liquid with a measurable boiling point, vapour exposure can be relevant during handling, particularly at elevated temperatures.
Odour: A reliable substance-specific odour description was not consistently reported in the principal sources reviewed.
Melting point: A reliable, consistently reported experimental melting point was not identified in the principal sources reviewed.
Solubility in organic media: As an aromatic organic isocyanate with Log P around 4, it is expected to have substantially greater compatibility with organic/lipophilic solvents than with water.
Beilstein: 2936403
CAS: 31027-31-3
Chemical Name or Material: 4-Isopropylphenyl isocyanate

DOT Information: Hazard Class: 6.1; Packaging Group: I
Density: 1.01
EINECS Number: 250-439-9
Flash Point: 90°C (194°F)
Formula Weight: 161.21
IUPAC Name: 1-isocyanato-4-propan-2-ylbenzene
InChI Key: PJVRNNRZWASOIT-UHFFFAOYSA-N
MDL Number: MFCD00013880
Molecular Formula: C10H11NO
PubChem CID: 94416
Recommended Storage: Keep cold

Refractive Index: 1.5205
SMILES: CC(C)C1=CC=C(C=C1)N=C=O
Sensitivity: Moisture sensitive
Linear Formula: C10H11O1N1
CAS Number: 31027-31-3
Molecular Weight: 161.2
MDL number: MFCD00013880
CBNumber: CB8719090
Molecular Formula: C10H11NO
Molecular Weight: 161.2

MDL Number: MFCD00013880
MOL File: 31027-31-3.mol
Boiling point: 85 °C4 mm Hg(lit.)
Density: 1.01 g/mL at 25 °C(lit.)
refractive index: n20/D 1.52(lit.)
Flash point: 195 °F
Water Solubility: decomposes
Sensitive: Moisture Sensitive
BRN: 2936403
LogP: 4.05 at 20℃
CAS DataBase Reference: 31027-31-3(CAS DataBase Reference)

FIRST AID MEASURES of P-ISOPROPYLPHENYL ISOCYANATE:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available

ACCIDENTAL RELEASE MEASURES of P-ISOPROPYLPHENYL ISOCYANATE:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.

FIRE FIGHTING MEASURES of P-ISOPROPYLPHENYL ISOCYANATE:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.

EXPOSURE CONTROLS/PERSONAL PROTECTION of P-ISOPROPYLPHENYL ISOCYANATE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.

HANDLING and STORAGE of P-ISOPROPYLPHENYL ISOCYANATE:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.

STABILITY and REACTIVITY of P-ISOPROPYLPHENYL ISOCYANATE:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature).
-Possibility of hazardous reactions:
No data available

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