Covestro Desmodur BL 3575/1 MPA/SN heat activated HDI curing agent low heat yellowing

Type

Based onHDIblocked aliphatic polyisocyanate

Form of Supply

about 75% solvent naphtha100 / 1-methoxy Arial-2(17:8

Purpose

withDesmophen®Brands can be used together to prepare light-resistant one-component baking polyurethane coatings

Specifications

Features

Value

Measurement unit

Method

Non-volatile ingredients (0.2 g/60 min/ 80°C)

75±2

<ssp; 160°C for 20 minutes
Or 170°C for 10 minutes
Or 190°C for 5 minutes
The use of metal catalysts can significantly reduce the baking temperature.
For coil coating systems, Desmodur® BL 3575/1 MPA/SN can achieve full crosslinking without catalyst addition at temperatures above 232°C.

Storage
– Store in original airtight Covestro container.
– Recommended storage temperature: 0-30°C.
– Protects against moisture, heat and foreign objects.
General Information: Storage at higher temperatures will result in increased color and viscosity. Will cause solidification on storage at significantly lower temperatures. By simply heating the product, this curing is reversible without adversely affecting product quality.

Storage Time
Covestro declares that the product will conform to the specifications or values ​​stated in the “Specifications or Characteristic Data” section within nine months of the day following shipment as stated in the shipping document” The above, applies, as long as the product is in full compliance with the storage conditions stated and referenced in the “Storage” section above and is otherwise properly handled. Expiration of the nine-month period does not necessarily mean that the product no longer meets specifications or settings values. However, prior to using the above-mentioned products, Covestro recommends testing whether such products still exist in compliance with specifications or set values. Covestro does not make any representations about the products after the nine-month period has expired. Xtron is not responsible or liable for meeting the specification or setpoint period after nine months have passed.

Labeling and Legal Requirements
This Product Data Sheet is used only in conjunction with the latest version of the corresponding Safety Data Sheet. Any updates to safety-related information, in accordance with statutory requirements, will only be reflected in the safety-related data sheets, copies of which will be revised and distributed. Related information to the current classification and labelling, application and treatment methods can be found in the currently valid safety data sheet for further safety-related data.

Lanxess Lanxess Trixene DP9C/213 HDI trimer water-based closed cross-linking agent

Water-based blocking crosslinker

Product name

Type

Sealer

Ion type

PH

Solid content (%)

Thinner

BI 200

HDI trimer

DMP

Anions

7-8

40

NMP

BI 201

HDI trimer

DMP

Anions

7-9

40

DME

BI 220

HDI trimer

DMP

Non-ionic

5-8

40

DIBA

DP9C/213

HDI trimer

Caprolactam

Anions

7-9

40

DME

DP9C/235

HDI trimer

MEKO

Anions

5-8

41.5

DIBA

DP9C/290

HDI trimer

DMP

cation

4-5

40

DME

DP9C/323

HDI&IPDI trimer

DMP

Non-ionic

5-8

40

DME

DP9C/347

HDI Biuret

DMP

Non-ionic

5-8

40

DIBA

Lanxess Lanxess Trixene BI 220 HDI trimer water-based closed cross-linking agent

Water-based blocking crosslinker

Product name

Type

Sealer

Ion type

PH

Solid content (%)

Thinner

BI 200

HDI trimer

DMP

Anions

7-8

40

NMP

BI 201

HDI trimer

DMP

Anions

7-9

40

DME

BI 220

HDI trimer

DMP

Non-ionic

5-8

40

DIBA

DP9C/213

HDI trimer

Caprolactam

Anions

7-9

40

DME

DP9C/235

HDI trimer

MEKO

Anions

5-8

41.5

DIBA

DP9C/290

HDI trimer

DMP

cation

4-5

40

DME

DP9C/323

HDI&IPDI trimer

DMP

Non-ionic

5-8

40

DME

DP9C/347

HDI Biuret

DMP

Non-ionic

5-8

40

DIBA

Lanxess Lanxess Trixene BI 201 HDI trimer water-based closed cross-linking agent

Water-based Blocking crosslinking agent

Product name

Type

Sealer

Ion type

PH

Solid content (%)

Thinner

BI 200

HDI trimer

DMP

Anions

7-8

40

NMP

BI 201

HDI trimer

DMP

Anions

7-9

40

DME

BI 220

HDI trimer

DMP

Non-ionic

5-8

40

DIBA

DP9C/213

HDI trimer

Caprolactam

Anions

7-9

40

DME

DP9C/235

HDI trimer

MEKO

Anions

5-8

41.5

DIBA

DP9C/290

HDI trimer

DMP

cation

4-5

40

DME

DP9C/323

HDI&IPDI trimer

DMP

Non-ionic

5-8

40

DME

DP9C/347

HDI Biuret

DMP

Non-ionic

5-8

40

DIBA

Lanxess Lanxess Trixene DP9B/1353 HDI trimer blocked crosslinker

Product name

Type

Sealer

Viscosity (mPa.s/25)

Solid content (%)

Solvent

Application

BI 7960

HDI Biuret

DMP

1100

70

PM

Coil steel/electroplating coating

BI 7961

HDI Biuret

DMP

2250

70

Naphta B

Coil steel/electroplating coating

BI 7963

HDI Biuret

DEM

4500

70

PM

Low temperature curing or highly reactive coatings

BI 7981

HDI trimer

450

65

PMA

Automotive/coil coating

BI 7982

HDI trimer

DMP

600

70

PM

Automotive/coil coating

BI 7984

HDI trimer

MEKO

3000

75

Naphta B

Coil/Industrial/Glass Coatings

BI 7991

HDI Biuret

DMP/DEM

1000

70

PM

Automotive/coil coating

BI 7992

HDI trimer

DMP/DEM

1500

70

PM

Automotive/coil coating

DP9B/1353

HDI trimer

DMP

4000

75

Shellsol A/PMA

Can/coil coating

BI 7950

IPDI adduct

DMP

1200

65

PM

Automotive/coil coating

BI 7951

IPDI trimer

DMP

3500

65

Naphta B/BA

Automotive/coil coating

Lanxess Lanxess Trixene BI 7992 HDI trimer closed crosslinker

Product name

Type

Sealer

Viscosity (mPa.s/25)

Solid content (%)

Solvent

Application

BI 7960

HDI Biuret

DMP

1100

70

PM

Coil steel/electroplating coating

BI 7961

HDI Biuret

DMP

2250

70

Naphta B

Coil steel/electroplating coating

BI 7963

HDI Biuret

DEM

4500

70

PM

Low temperature curing or highly reactive coatings

BI 7981

HDI trimer

450

65

PMA

Automotive/coil coating

BI 7982

HDI trimer

DMP

600

70

PM

Automotive/coil coating

BI 7984

HDI trimer

MEKO

3000

75

Naphta B

Coil/Industrial/Glass Coatings

BI 7991

HDI Biuret

DMP/DEM

1000

70

PM

Automotive/coil coating

BI 7992

HDI trimer

DMP/DEM

1500

70

PM

Automotive/coil coating

DP9B/1353

HDI trimer

DMP

4000

75

Shellsol A/PMA

Can/coil coating

BI 7950

IPDI adduct

DMP

1200

65

PM

Automotive/coil coating

BI 7951

IPDI trimer

DMP

3500

65

Naphta B/BA

Automotive/coil coating

Costron (formerly Bayer) Desmodur 44C Pure MDI 101-68-8

Product Description
DESMODUR 44C is a 4,4′-diphenylmethane diisocyanate monomer with a molecular weight of 250 and is a colorless to light yellow solid at room temperature. This product is mainly used in the production of polyurethane products.

Sampling
Prevent the product from coming into contact with water vapor during sampling.

Specification

Item

Indicator

Unit

Test Method

2,4′-MDI content

≤1.8

% of

20110367601-92

Hydrolyzed chloride content

≤50

ppm

2011-0339304-95

Dimer content*

≤0.1

% of

2012-0346901-92

Typical properties

Item

Indicator

Unit

Test method

Purity (molecular weight 250)

≥99.5

% of

2011-0248603-94

NCO content (theoretical value)

33.6

% of NCO content (theoretical value)

Phenyl isocyanate content

≤10

ppm

2011-0339304-95

Viscosity (40℃)

0.1

mPa.s

2011-0313703-95

Density (40℃)

1.19

g/cm³

DIN 51757

Specific heat (cp)

Approx. 1.39

kJ/kg.K

Heat of dissolution

Approx. 102

J/g

Packaging
DESMODUR 44C is available in two ways:
– Liquid (tanker truck)
– Solid (in drums, net weight 225 kg)

Storage

Recommended storage temperature (°C)

<5 (solid), 43±2 (liquid)

Shelf life

≤3 months (solid), ≤3 weeks in tank (liquid) if kept in closed, drained condition

Handling Recommendations
Like all isocyanates, DESMODUR 44C is very sensitive to water and reacts with water to produce insoluble urea and carbon dioxide. In a closed container, the carbon dioxide produced can cause a dangerous rise in container pressure.
Exposure of DESMODUR 44C to air, especially sunlight, accelerates yellowing. It is therefore recommended that liquid DESMODUR 44C be stored in a dry nitrogen atmosphere. yellowing will not normally affect the processability of the product.
DESMODUR 44C is heat sensitive and can form dimers. DESMODUR 44C in the solid state is more susceptible to dimerization at room temperature than in the liquid state at 45°C. For this reason, it is important to store DESMODUR 44C in the solid state at room temperature. Therefore, solid products should be stored below 5°C and melted gradually and rapidly before use. Although the rate of dimerization of the product decreases with decreasing temperature, the stability is still limited even at temperatures below 5℃.
Solid DESMODUR 44C needs to be heated to ≥70°C for melting, a process that will increase the formation of insoluble dimers and possibly deform the drum due to increased pressure at increased temperatures.

Evonik Vestanat IPDI isophorone diisocyanate 4098-71-9

Manufacturer :EVONIK Degussa

Structure: 3-isocyanatomethyl-3,5,5-trimethylcyclohexyl isocyanate

Physical properties

Properties

Numerical value

Unit

Test method

Density (20℃)

1.058-1.064

g/cm3

DIN51757ASTMD2111

Viscosity (23℃)

13-15

mPa-s

DINENISO3219

Color (APHA)

<30

DIN/ISO6271

Refractive index (N25D)

1.483

DIN51423 Part II

Vapor pressure (50°C)

Approx. 0.02

hPa

Flash point (closed cup)

155

flash point (closed cup) 155 ºC

DIN51758

Flash Point

430

Ignition point 430 ºC

DIN51794

Specification

Properties

Numerical value

Unit

Test Method

NCO content

37.5-37.8

%Weight

ENISO11909ASTMD2572

Purity

>99.5

%Weight

Gas Chromatography

Total Chlorine

<400

ppm

Hydrolyzed Chlorine

<200 ppm

ppm

Evonik IPDI Properties and Applications
The alicyclic diisocyanate VESTANAT®IPDI meets all the necessary conditions for the production of light-stable and weather-resistant polyurethanes. The selection of the appropriate co-reactants (polyols) gives the polyamino acid system a high degree of resistance to yellowing and properties typical of polyurethanes, such as good mechanical and chemical resistance. In addition, IPDI has many advantages in the polyurethane process due to its inherent properties.
Since VESTANAT®IPDI contains two different isocyanate functional groups, it presents selectivity in ammonia esterification reactions, e.g. in the synthesis of pre-polymers, resulting in good reproducibility. The selective formation of the desired product narrows the molecular weight distribution, reduces the viscosity and also reduces the residual concentration of the starting monomer diisocyanate (IPDI). As a raw material for polyurethanes, IPDI and its polyisocyanates and prepolymers are known for their excellent miscibility with other resins and good solubility in a variety of general-purpose solvents such as ketones, esters, ethers, and aromatics. Good solubility and miscibility in aliphatic hydrocarbons such as petroleum solvents is also exceptional.

From a technical point of view, VESTANAT® IPDI is an important starting isocyanate for the production of raw materials for polyurethane paints. It is used in various polyurethane paint systems in different forms. Other important uses are solvent-free, light-stabilized polyurethane injection molding technology (RIM) and water-based adhesives or hot melt glues. In polyurethane resin technology, the preparation of waterborne polyurethane dispersions is the most important application of VESTANAT®IPDI, since low viscosity prepolymers and end products with low co-solvent content can be produced from this starting material. It is a hard segment component of the resin. Polyurethane acrylates synthesized on the basis of VESTANAT®IPDI for radiation curing (conventional or aqueous) can be chosen if excellent yellowing resistance and low reactive diluent or co-solvent content are required.
VESTANAT®IPDI can be used in moisture-curing prepolymers, another application for polyurethane resins, and IPDI can characterize these products with resistance to yellowing, low viscosity and low diisohydrogenate monomer residues. Solvent-borne, high-molecular-weight polyurethane resins based on VESTANAT® IPDI can be used in coatings where abrasion resistance is required, especially where long-term flexibility and light resistance are required. Typical applications are polyurethane resins for artificial leather or natural leather finishes. The polyurethanatization of alkyd resins with IPDI to produce ammonia ester alkyds and ammonia ester oils is mainly used to sufficiently improve the yellowing resistance, drying properties and hardness of these resins.

In the two-component polyurethane sector, VESTANAT® IPDI is used either as an adduct with tertiary alcohols (e.g. adducts with TMP) or in the form of polyisocyanates (e.g. VESTANAT® T1890). This application is mainly used in large vehicle and automotive coatings (OEM and refinish).

VESTANAT®IPDI and its polyisocyanates are used to prepare closed polyisocyanates that can be used as crosslinkers in electrostatically sprayed powder coatings and solvent-borne industrial paints, especially for can coating and coil coating. IPDI-based crosslinkers give solvent-free two-component polyurethanes good light stability and mechanical properties. These systems are mainly used for elastomeric coatings and casting resins. Hard systems can be used as industrial materials.

Reactive and Catalytic
Aliphatic and alicyclic diisocyanates are less reactive than aromatic ones.IPDI usually requires a suitable catalyst to accelerate the ammonia esterification reaction. Dibutyltin dilaurate is recommended as a catalyst for ammonia esterification.
Dibutyltin dilaurate is often used when VESTANAT® IPDI or adducts of this product are used as ambient temperature crosslinkers in polyurethane formulations. Where a complete or partial reaction of isocyanate and water (moisture) is required, a catalyst mixture of dibutyltin dilaurate and a tertiary amine such as diazodicarbocyclooctane (DABCO) should be used. In addition to dibutyltin dilaurate, iron acetylacetonate, phenylmercury salt (COSCATR83) is an effective catalyst for solvent-free polyurethanes (elastomers and casting resins). Of course at high temperatures, resin synthesis, i.e. production of prepolymers, is possible without a catalyst for the reaction. When the temperature is increased, the difference between the two isocyanate activities of IPDI decreases, so that the production of prepolymers is more selective when a catalyst is employed at room temperature. The best selectivity can be achieved at temperatures up to 50°C and with the addition of DBTDL.

Storage and transportation
VESTANAT® IPDI is supplied in non-recyclable 30 kg cans and 200 kg drums, but also in tankers and storage tanks. If moisture can be removed, IPDI can be stored for at least one year without affecting the quality of the above standards. Long-term storage may increase the color index.

Crestron (formerly Bayer) Desmodur I Isophorone Diisocyanate IPDI 4098-71-9

Chemical name : 3-Isocyanatomethyl-3,5,5-trimethylcyclohexyl isocyanate

Alias : 3-Isocyanatomethyl-3,5,5-trimethylcyclohexyl isocyanate; 5-Isocyanato-1-(isocyanatomethyl)-1,3,3-trimethylcyclohexane; IPDI

IPDI products are mixtures containing 75% cis and 25% trans isomers.

Molecular Formula

C12H18N2O2

Relative Molecular Mass

222.29.CAS

CAS No.

4098-71-9.

EINECS No.

223-861-6

Physical and Chemical Properties

Isophorone Diisocyanate IPDI is colorless or light yellow liquid with camphor-like odor, completely miscible with esters, ketones, ethers, aromatic hydrocarbons and aliphatic hydrocarbons and other organic solvents.

Density

1.056

Melting point

– 60°C

Boiling point

158°C (15 mmHg)

Refractive index

1.484

Flash Point

>110°C

Water Solubility

<0.1 g/100 mL at 25°C

Performance Indicators

The specifications for IPDI products (brand name Desmodur I) are:

Purity

≥99.5 %

Mass fraction of NCO

≥37.5%

Color (Hazen)

≤30

Hydrolyzed chlorine

≤200 mg/kg

Total chlorine

≤400 mg/kg

Viscosity (25℃)

Approx. 10 mPa-s.

Safety data

Hazardous material symbol

T;N

Hazardous category code

r22;r36/37/38;r42/43;r51/53

Safety instructions

s26;s28;s38;s45;s61

Dangerous Goods Transportation Number

UN 2290/2906

Properties and Uses

IPDI is an aliphatic isocyanate, isophorone diisocyanate IPDI is also a kind of cycloaliphatic isocyanate, isophorone diisocyanate IPDI reactivity is lower than the aromatic isocyanate, and the vapor pressure is also lower. The reactivity of 2 NCO groups in isophorone diisocyanate IPDI molecule is different, because the primary NCO in IPDI molecule is hindered by the cyclohexane ring and a-substituted methyl group, which makes the reactivity of the secondary NCO group connected to cyclohexane is 1.3-2.5 times higher than that of the primary NCO; the reactivity of IPDI and hydroxyl group is 4-5 times faster than that of HDI and hydroxyl group.
The polyurethane resin made of isophorone diisocyanate IPDI has excellent light stability and chemical resistance, isophorone diisocyanate IPDI is generally used in the manufacture of high-grade polyurethane resins, such as light-resistant and marble-resistant polyurethane coatings, abrasion-resistant and hydrolysis-resistant polyurethane elastomers, and isophorone diisocyanate IPDI is also used in the manufacture of non-yellowing microcellular polyurethane foam.

Lanxess Lanxess Trixene DP9C/290 HDI trimer water-based closed crosslinker

Water-based Blocked cross-linking agent

Product name

Type

Sealer

Ion type

PH

Solid content (%)

Thinner

BI 200

HDI trimer

DMP

Anions

7-8

40

NMP

BI 201

HDI trimer

DMP

Anions

7-9

40

DME

BI 220

HDI trimer

DMP

Non-ionic

5-8

40

DIBA

DP9C/213

HDI trimer

Caprolactam

Anions

7-9

40

DME

DP9C/235

HDI trimer

MEKO

Anions

5-8

41.5

DIBA

DP9C/290

HDI trimer

DMP

cation

4-5

40

DME

DP9C/323

HDI&IPDI trimer

DMP

Non-ionic

5-8

40

DME

DP9C/347

HDI Biuret

DMP

Non-ionic

5-8

40

DIBA