PRODUCTS

FLOCRYL NMA

Flocryl NMA is used in the following areas: agriculture, forestry and fishing and formulation of mixtures and/or re-packaging.
Flocryl NMA is used for the manufacture of: chemicals and textile, leather or fur.
Flocryl NMA is used as a crosslinker or functional monomer in water treatment applications.

CAS Number: 924-42-5
EC Number: 213-103-2
MDL Number: MFCD00004597
IUPAC Name: N-(hydroxymethyl)prop-2-enamide
Molecular formula: C4H7NO2

SYNONYMS:
NMA, N-Methylolacrylamide, Acrylamide methylol derivative, Crosslinking monomer, Methanol-stabilized NMA, Flocculant enhancer, Polymer crosslinker, Functional acrylamide derivative, N-(hydroxymethyl)prop-2-enamide, N-(Hydroxymethyl)acrylamide, n-Methylolacrylamide, METHYLOLACRYLAMIDE 45%, MLAM 48%, Flocryl NMA 48, N-MAM 60 S (200), AEROTEX NMA LF, NMA monomer 48 % in water, N-Methylolacrylamide 48 (NMA 48), N-Methylolacrylamide, N-(Hydroxymethyl)acrylamide, NCI-C60333, N-MAM, NM-AMD, N-Methanolacrylamide, N-Methyloacrylamide, 2-Propenamide, N-(hydroxymethyl)-, Acrylamide, N-(hydroxymethyl)-, Methylolacrylamide, Monomethylolacrylamide, Monomethylolacrylamide NMA, N-(Hydroxymethyl) acrylamide, N-(Hydroxymethyl)-2-propenamide, NSC 553, Uramine T 80, Yuramin T 80, 2-Propenamide, N-(hydroxymethyl)-, Acrylamide, N-(hydroxymethyl)-, Hydroxymethylacrylamide, Methylolacrylamide, Monomethylolacrylamide, N-(Hydroxymethyl)-2-propenamide, N-(Hydroxymethyl)acrylamide, N-Hydroxymethyl acrylamide, N-Methanolacrylamide, Uramine T 80, Acrylamide, N-(hydroxymethyl)-, Monomethylolacrylamide, N-(Hydroxymethyl)acrylamide, N-Methanolacrylamide, N-Methylolacrylamide, Uramine T 80, Yuramin T 80, Methylolacrylamide, N-(Hydroxymethyl)-2-propenamide, NCI-C60333, N-Methyloacrylamide, NM-AMD, NSC 553, N-MAM, Acrylamide, N-(hydroxymethyl)- (6CI,8CI), N-(Hydroxymethyl)-2-propenamide, Cylink NMA, MH 100, MH 100 (amide), Monomethylolacrylamide, N-(Hydroxymethyl)acrylamide, N-MAM, N-MAM P, N-Methanolacrylamide, N-Methylolacrylamide, N-NBM, NMA 60, NSC 553, Rocagil BT, U-Ramin T, 80 METHYLOLACRYLAMIDE, n-(hydroxymethyl)-2-propenamide, N-(HYDROXYMETHYL)ACRYLAMIDE, N-METHYLOLACRYLAMIDE, 2-Propenamide,N-(hydroxymethyl)-, Acrylamide, N-(hydroxymethyl)-, Monomethylolacrylamide, n-(hydroxymethyl)-2-propenamid, n-(hydroxymethyl)-acrylamid, NCI-C60333, NM-AMD, N-Methanolacrylamide, N-Methyloacrylamide, n-methylolacrylamide(48%inwater), Uramine T 80, uraminet80, Yuramin T 80, Methylolacrylamidesolution, N-MAN, N-(HYDROXYMETHYL)ACRYLAMIDE SOLUTION, ST AB., ~48% IN H2O, 2-Propenamide,N-(hydroxymethyl)-, Acrylamide,N-(hydroxymethyl)-, N-(Hydroxymethyl)-2-propenamide, N-Methylolacrylamide, N-Methanolacrylamide, N-(Hydroxymethyl)acrylamide, Monomethylolacrylamide, NMA 60, MH 100 (amide), MH 100, N-MAM P, U-Ramin T 80, Rocagil BT, N-MAM, NSC 553, N-NBM, Cylink NMA, N-Methylol acrylamide, NMA 48, 90456-67-0, 160278-55-7, 176598-18-8, 194091-52-6, 211862-48-5, 211862-50-9, 2-Propenamide,N-(hydroxymethyl)-, Acrylamide,N-(hydroxymethyl)-, N-(Hydroxymethyl)-2-propenamide, N-Methylolacrylamide, N-Methanolacrylamide, N-(Hydroxymethyl)acrylamide, Monomethylolacrylamide, NMA 60, MH 100 (amide), MH 100, N-MAM P, U-Ramin T 80, Rocagil BT, N-MAM, NSC 553, N-NBM, Cylink NMA, N-Methylol acrylamide, NMA 48, 90456-67-0, 160278-55-7, 176598-18-8, 194091-52-6, 211862-48-5, 211862-50-9, N-(Hydroxymethyl)acrylamide, 2-Propenamide, N-(hydroxymethyl), N-(Hydroxymethyl)-2-propenamide, N-Methylol acrylamide, N-Methanolacrylamide, n-(hydroxymethyl)-2-propenamide, N-methanolacrylamide, Monomethylolacrylamide, NCI-C60333, Uramine T 80, N-(HYDROXYMETHYL)ACRYLAMIDE, N-Methylolacrylamide, 924-42-5, Methylolacrylamide, N-Methylol Acrylamide, N-Methanolacrylamide, Monomethylolacrylamide, 2-Propenamide, N-(hydroxymethyl)-, N-Hydroxymethyl acrylamide, Acrylamide, N-(hydroxymethyl)-, Uramine T 80, N-(hydroxymethyl)prop-2-enamide, N-(Hydroxymethyl)-2-propenamide, Hydroxymethylacrylamide, N-MAM, N-Methyloacrylamide, NCI-C60333, Yuramin T 80, CCRIS 2380, NM-AMD, HSDB 4361, NSC 553, EINECS 213-103-2, UNII-W8W68JL80Q, BRN 0506646, AI3-25447, NSC-553, METHYLOLACRYLAMIDE, N-, W8W68JL80Q, DTXSID3020885, CHEBI:82492, EC 213-103-2, N-METHYLOLACRYLAMIDE [IARC], MFCD00004597, N-(HYDROXYMETHYL)ACRYLAMIDE [HSDB], N-METHYLOLACRYLAMIDE (IARC), N-hydroxymethylacrylamide, NMethanolacrylamide, ROCAGIL BT, NHydroxymethyl acrylamide, N(Hydroxymethyl)acrylamide, N-MAM P, N(Hydroxymethyl)2propenamide, Acrylamide, N(hydroxymethyl), N-(hydroxymethyl) acrylamide, SCHEMBL25806, U-RAMIN T 80, DTXCID90885, 2Propenamide, N(hydroxymethyl), MH 100 (AMIDE), NMA 60, NSC553, CHEMBL1892361, N-(Hydroxymethyl)acrylamide 100 microg/mL in Acetonitrile, MH 100, AKOS006222324, CS-W013710, NCGC00163845-01, NCGC00163845-02, BS-17859, M0574, NS00008229, C19456, E78933, EN300-7474805, W-100289, Q26840808, uraminet80, Yuramin T 80, METHYLOLACRYLAMIDE, N-METHYLOLACRYLAMIDE, N-Methylol acrylamide, Methylolacrylamidesolution, N-(HYDROXYMETHYL)ACRYLAMIDE, N-(Hydroxymethyl)acrylamide, n-(hydroxymethyl)-2-propenamide

Flocryl NMA because of its molecular structure contains two reactive groups, a polymerizable double bond and a condensable methylol
Group, Flocryl NMA therefore has the characteristics of a crosslinking agent monomer.
The earliest synthetic method was to react acrylamide with formaldehyde to obtain crystalline Flocryl NMA.

For example, foreign scholars use paraformaldehyde and acrylamide crystals, trichloroethylene as solvent, and metal sodium colloid as catalyst to produce Flocryl NMA.
After the reaction is finished, the system naturally divides into two phases.

When the temperature is lowered to room temperature, Flocryl NMA precipitates in a large amount, and Flocryl NMA is obtained, but the obtained product needs to be recrystallized with acetone or ethyl acetate.
Flocryl NMA is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 000 to < 10 000 tonnes per annum.

Flocryl NMA is a colorless or yellow liquid.
Flocryl NMA is White solid.
Flocryl NMA is a versatile and widely used chemical compound in various industries.

Flocryl NMA is a monomer that possesses unique crosslinking properties, making it valuable in different applications.
Flocryl NMA is a white solid
Flocryl NMA appears as a colorless or yellow aqueous solution.

Flocryl NMA appears as a colorless or yellow aqueous solution.
Flocryl NMA is a secondary carboxamide.
Flocryl NMA is a self-bred active monomer.

In the molecular structure, Flocryl NMA has a dual and active functional group conjugated with hydroxyl groups.
Flocryl NMA is very soluble in water and alcohol, and is hardly soluble in chloroform and tetrachloride.
Carbon, Flocryl NMA is easy to self-polymerize and cross-link into insoluble resin in humid air, especially under acidic conditions.

Flocryl NMA is an ideal raw material for a wide variety of applications.
Flocryl NMA is especially suitable for the preparation of latex binders and of cross-linkable emulsion polymers used in.

Flocryl NMA is used Adhesives, Antistatic agents, Chromatographic materials, Catalysts, Impregnation of non-woven fabrics, Inks, Paints, Paper coatings, Pasting agents, Plastics, Rubbers, Soil grouting systems, Textile finishes, Thermoplastics resins.

When properly copolymerised, Flocryl NMA forms latices which have low viscosity and excellent shelf stability.
When the films, formed from these lattices, are cured, they develop excellent water resistance, organic solvent resistance, adhesion at
high humidity and flexibility.

Flocryl NMA is a reactive monomer.
As with other such monomers, Flocryl NMA must be stabilized to prevent polymerisation during shipping and storage.

Flocryl NMA can be safely handled if inhibited with cupric ions and oxygen, and if temperature, pH, and contamination are controlled.
Air is usually an adequate source of oxygen.

USES and APPLICATIONS of FLOCRYL NMA:
Flocryl NMA molecule has double bond conjugated with carbonyl and reactive hydroxymethyl, it is a widely used cross-linking monomer for fiber modification, resin processing, adhesives and paper, leather, metal surface treatment agents, but also for soil amendments.

Flocryl NMA can be used as crosslinking agent, widely used in fiber modification resin, processing dye, plastic adhesive, soil stabilizer, etc.
Organic synthetic monomer, Flocryl NMA, can be used to prepare a variety of copolymers.

Flocryl NMA has two active groups in its molecular structure, which are polymerizable double bonds and condensable methylol groups, therefore, it has the characteristics of crosslinking agent monomer and is widely used in the fields of fiber modification, resin processing, coatings, plastics, adhesives, oil field additives and soil amendments.

In addition, Flocryl NMA can also be polymerized with a variety of monomers in an aqueous system to prepare a polymer with excellent performance, which is a fine chemical widely used at present.
Foreign research and application of this technology is relatively mature, the domestic application is still very limited, many applications still need further research and development, Flocryl NMA can also play a greater potential and value.

When the temperature is lowered to room temperature, Flocryl NMA precipitates in a large amount, and Flocryl NMA is obtained, but the obtained product needs to be recrystallized with acetone or ethyl acetate.
Flocryl NMA is used in formulation or re-packing, at industrial sites and in manufacturing.

Release to the environment of Flocryl NMA can occur from industrial use: formulation of mixtures.
Flocryl NMA is used in the following products: polymers.
Flocryl NMA has an industrial use resulting in manufacture of another substance (use of intermediates).

Flocryl NMA is used in the following areas: agriculture, forestry and fishing and formulation of mixtures and/or re-packaging.
Flocryl NMA is used for the manufacture of: chemicals and textile, leather or fur.
Release to the environment of Flocryl NMA can occur from industrial use: as an intermediate step in further manufacturing of another substance (use of intermediates), for thermoplastic manufacture and as processing aid.

Release to the environment of Flocryl NMA can occur from industrial use: manufacturing of the substance.
Flocryl NMA is used as a crosslinker or functional monomer in water treatment applications.
Flocryl NMA enhances the performance of flocculants in industrial and municipal wastewater treatment.

Flocryl NMA is applied in paper manufacturing to improve retention and drainage.
Flocryl NMA is used in adhesives, coatings, and textiles for crosslinking purposes.
This versatile compound, Flocryl NMA, finds applications in the production of adhesives, coatings, and textiles, where its cross linking capabilities play a crucial role in improving product performance.

Flocryl NMA is used Textile Industry, Paper Industry, Coatings and Paints, Adhesives, Personal Care and Cosmetics, and Polymer Industry.
Flocryl NMA is used in adhesives, binders, surface coatings, and resins.
Flocryl NMA is used as a starch modifier;

Flocryl NMA uses and applications include: Starch modifier; reactive comonomer for vinyl acetate, SB resins.
Suggested storage of Flocryl NMA: Light-sensitive
The Applications of Flocryl NMA rabge from adhesives and binders in papermaking,textile,and non-wovens to a variety of surface coating and resin for varnishes,films and sizing agents.

Flocryl NMA can be used as a cross-linking agent, widely used in fiber modified resin, processing dyes, plastic adhesives, soil stabilizers, etc
Flocryl NMA is used chemical intermediate, reactive comonomer; production of polymers for coatings, varnishes, and adhesion; crease resistance in cotton material.

PHYSICAL AND CHEMICAL PROPERTIES OF FLOCRYL NMA:
Flocryl NMA is character white powder, soluble in water or hydrophilic solvent, but insoluble in hydrocarbon halogenated hydrocarbon and other solvents, unstable in humid air or water, easy polymerization, when heated in the presence of acid in aqueous solution, it will rapidly polymerize into insoluble resin

PROPERTIES OF FLOCRYL NMA:
*strong crosslink bonds in polymers
*resulting in enhanced adhesion
*mechanical strength
*durability of the final products

APPLIATION AREAS OF FLOCRYL NMA:
*Polymerization
*Adhesives and Binders
*Water Treatment
*Textile Industry
*Personal Care Products
*Crosslinking Agent

BENEFITS OF FLOCRYL NMA:
*Flocryl NMA improves flocculation efficiency in wastewater and industrial applications.
*Flocryl NMA enhances the mechanical strength and durability of treated products.
*Versatile across a range of applications, including adhesives and coatings.

PRODUCTION METHOD OF FLOCRYL NMA:
under weak alkaline conditions, acrylamide is prepared by reacting with 37% formaldehyde in water.

PREPARATION OF FLOCRYL NMA:
(1), acrylamide is added to the reaction kettle filled with solvent acetone, raise the temperature to 42~45 ℃;
(2), add the catalyst sodium methoxide, adjust the pH value of the reaction solution to 8.88;
(3), add formaldehyde, adjust the pH value of the reaction solution to 8.5, the reaction was carried out at a constant temperature for 1 hour;
(4) phthalic acid was added to adjust the pH of the reaction solution to 7.2;
(5) the reaction solution was cooled, crystallized and filtered to obtain the finished Flocryl NMA.

REACTIVITY OF FLOCRYL NMA:
Flocryl NMA is supplied as a 48% solution in water.
Flocryl NMA's reactivity is due to the presence in the molecule of both an unsaturated vinyl group and a hydroxymethyl group which can be reacted separately and/or independently simply by varying the reaction conditions.

*Reaction of the vinyl group
Flocryl NMA can be used in the preparation of a wide range of polymers and copolymers.
The main is free radical polymerisation with other vinyl monomers such as acrylonitrile, acrylamide, acrylic and methacrylic
esters, vinyl chloride, and styrene which leaves the hydroxymethyl group available.

Additionally, the double bond in Flocryl NMA can be reacted with both halogens and alcohols under alkaline conditions and
with thiol in the presence of alcoholate.

*Reaction of the hydroxymethyl group
The hydroxymethyl group has a tendency to undergo condensation or substitution reactions.
Flocryl NMA containing polymers can be crosslinked either with themselves or with other reactive monomers, by heating and/or by the presence of an acid catalyst

STORAGE OF FLOCRYL NMA:
tanks should include temperature monitoring and an independent temperature alarm system for early detection of polymerisation.

OXYGEN
Dissolved oxygen is necessary to inhibit polymerisation of Flocryl NMA.
The dissolved oxygen level together with the air present is quite adequate stabilization during storage.
Controlled intermittent air flow or continuous sparging at 0.09 Nm3/hr per m3 of Flocryl NMA (0.2 SCFM per thousand gallons) is sufficient for inhibition purposes.

TEMPERATURE
Flocryl NMA should be controlled to between 0°C (32°F) and 30°C (86°F).
At temperatures below –10°C (14°F), N-methylolacrylamide will crystallize and separate from the solution.
Warming the product to 0°C (32°F) will re-dissolve the crystals.

In storage tanks, railcars and tank trucks, introduce tempered water
(maximum temperature 40°C (104°F)) into the heating coils.
Packaged material should be moved to a warm environment until crystals are redissolved.

Do not apply steam to heating coils or direct heat to packaged material.
Hot spots must be avoided.

An air sparge should be employed, and agitation will increase the rate of dissolution.
At temperatures above 50°C (120°F), polymerisation could be initiated over time.

*pH
As supplied, Flocryl NMA has a pH of 6.0 to 7.0.
Any modification of the pH, above or below these specifications can reduce the stability significantly.
Periodic monitoring of pH is recommended and, if necessary,
the pH should be adjusted with either dilute sodium hydroxide or dilute sulfuric acid, or any other appropriate acids or bases.

*CONTAMINATION
As with other reactive monomers, contamination of Flocryl NMA solutions with known initiators such as peroxides and azo compounds must be avoided.
Strong oxidizing agents such as persulfates can also initiate polymerisation of Flocryl NMA.
Reducing agents such as sulfites and bisulfites under certain conditions, can cause polymerisation.

*EFFECT OF LIGHT
Flocryl NMA is UV (ultra violet) sensitive.
Therefore, Flocryl NMA should not be exposed to direct sunlight or polymerisation may occur.

OPERATIONAL NOTES OF FLOCRYL NMA:
*Storage
Flocryl NMA is a reactive monomer which can polymerise spontaneously with the possible generation of heat and pressure, in the presence of certain contaminants, or as a result of improper handling or storage.

As with any toxic or reactive material, thorough training of all employees is imperative.
Knowledge of the toxicological properties, strict provisions for safe handling procedures and appropriate storage and handling
practices are necessary for ensuring the safe use of this monomer.

It is recommended that Flocryl NMA be used before six months after the date of manufacturing.
Do not sparge or blanket

Flocryl NMA with an inert gas.
Shelf life may be reduced if these storage conditions are not observed.

PHYSICAL and CHEMICAL PROPERTIES of FLOCRYL NMA:
Chemical Nature: Polymer or monomer-based product, typically containing N-methylolacrylamide.
Appearance: Clear or slightly cloudy liquid or solid, depending on formulation.
Molecular Formula (NMA): C4H7NO2
Molecular Weight (NMA): 101.1 g/mol
Density: Approx. 1.1 g/cm³ (may vary with composition).
Solubility: Soluble in water.
Thermal Stability: Decomposes at elevated temperatures.
pH: Dependent on formulation, typically 4–8.
Appearance: Clear to slightly yellowish solution
Molecular weight (g.mol-1): 101.10
Active content (%): 48.0
Refractive index (%): 1.412

Heat of polymerisation (Kcal/mole): 20.0
Specific gravity at 25°C: 1.08
Cristallization point (°C): -10
Molecular Weight: 101.10 g/mol
XLogP3-AA: -0.5
Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 2
Exact Mass: 101.047678466 g/mol
Monoisotopic Mass: 101.047678466 g/mol
Topological Polar Surface Area: 49.3Å²

Heavy Atom Count: 7
Formal Charge: 0
Complexity: 79.8
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Product Name: N-Methylolacrylamide
CAS No.: 924-42-5
Molecular Formula: C4H7NO2
InChIKeys: InChIKey=CNCOEDDPFOAUMB-UHFFFAOYSA-N
Molecular Weight: 101.10400
Exact Mass: 101.10
EC Number: 213-103-2
UNII: W8W68JL80Q
ICSC Number: 1637
NSC Number: 553
PSA: 49.33000
XLogP3: -0.37070
Appearance: N-methylolacrylamide appears as a colorless or
yellow aqueous solution.

Density: 1.074
Melting Point: 74.5 °C
Boiling Point: 318.1ºC at 760mmHg
Flash Point: 146.2ºC
Refractive Index: n20/D 1.413
Water Solubility: Solubility in water, g/100ml at 20°C: 188
Storage Conditions: Refrigerator
Vapor Pressure: Vapour pressure, Pa at 25°C: 0.03 (negligible)
Air and Water Reactions: Soluble in water.
Reactive Group: Alcohols and Polyols
Reactivity Alerts: Polymerizable

Molecular weight (g.mol-1 ): 101.10
Active content (%): 48.0
Refractive index (%): 1.412
Heat of polymerisation (Kcal/mole): 20.0
Specific gravity at 25°C: 1.08
Cristallization point (°C): -10
Product Number: M0574
Purity / Analysis Method: >98.0%(T)
Molecular Formula / Molecular Weight: C4H7NO2 = 101.11
Physical State (20 deg.C): Solid
Storage Temperature: 0-10°C

Condition to Avoid: Light Sensitive,Heat Sensitive
CAS RN: 924-42-5
Reaxys Registry Number: 506646
PubChem Substance ID: 87572604
SDBS (AIST Spectral DB): 1581
MDL Number: MFCD00004597
Physical state: liquid
Color: colorless, yellow
Odor: formaldehyde-like
Melting point/freezing point:
Melting point/range: -10 °C
Initial boiling point and boiling range: No data available
Flammability (solid, gas): No data available

Upper/lower flammability or explosive limits: No data available
Flash point: > 93 °C - closed cup
Autoignition temperature: Not applicable
Decomposition temperature: No data available
pH: 6,0 - 7,0
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility at 20 °C soluble
Partition coefficient: n-octanol/water: No data available
Vapor pressure: 31,68 hPa at 25 °C

Density: 1,074 g/cm3 at 25 °C
Relative density: No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: Not classified as explosive.
Oxidizing properties: none
Other safety information: No data available
Solubility: 1880 g/l (20 °C)
Melting Point: -10 °C
Boiling Point: 100 °C (1013 hPa)
Vapor Pressure: 31 hPa (25 °C)
Flash Point: 93 °C
Density: 1.08 g/cm3 (20 °C)
pH: 6.0 - 7.0 (H2O, 20 °C)

Assay (ex N): 48 - 50%
Identity (IR): Passes test
Storage temperature: 15 °C
Molecular Weight: 101.10400
Exact Mass: 101.10
EC Number: 213-103-2
UNII: W8W68JL80Q
ICSC Number: 1637
NSC Number: 553
DSSTox ID: DTXSID3020885
HScode: 2924199090
PSA: 49.33000
XLogP3: -0.37070

Appearance: N-methylolacrylamide appears as a colorless or
yellow aqueous solution.
Density: 1.074
Melting Point: 74.5 °C
Boiling Point: 318.1ºC at 760mmHg
Flash Point: 146.2ºC
Refractive Index: n20/D 1.413
Water Solubility: Solubility in water, g/100ml at 20°C: 188
Storage Conditions: Refrigerator
Vapor Pressure: Vapour pressure, Pa at 25°C: 0.03 (negligible)
Air and Water Reactions: Soluble in water.

Reactive Group: Alcohols and Polyols
Reactivity Alerts: Polymerizable
CAS: 924-42-5
EINECS: 213-103-2
InChI: InChI=1/C4H7NO2/c1-3(2-6)4(5)7/h6H,1-2H2,(H2,5,7)
InChIKey: CNCOEDDPFOAUMB-UHFFFAOYSA-N
Molecular Formula: C4H7NO2
Molar Mass: 101.1
Density: 1.082g/mL at 20°C
Melting Point: 74-75°C
Boling Point: 277°C(lit.)
Flash Point: 100°C
Water Solubility: <0.1 g/100 mL at 20.5 ºC

Solubility: Chloroform (Slightly), Methanol (Slightly)
Vapor Pressure: 31 hPa (25 °C)
Appearance: Solid
Specific Gravity: 1.074
Color: White to Off-White
BRN: 506646
pKa: 13.25±0.10 (Predicted)
PH: 6.0-7.0 (H2O, 20°C)
Storage Condition: Store at <= 20°C.
Stability: Light Sensitive, Moisture Sensitive
Sensitive: Sensitive to light
Refractive Index: n20/D 1.413
MDL: MFCD00004597

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

ACCIDENTAL RELEASE MEASURES of FLOCRYL NMA:
-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 carefully with liquid-absorbent material.
Dispose of properly.
Clean up affected area.

FIRE FIGHTING MEASURES of FLOCRYL NMA:
-Extinguishing media:
*Suitable extinguishing media:
Use extinguishing measures that are appropriate to local circumstances and the surrounding environment.
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Suppress (knock down) gases/vapors/mists with a water spray jet.
Prevent fire extinguishing water from contaminating surface water or the ground water system.

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

HANDLING and STORAGE of FLOCRYL NMA:
-Precautions for safe handling:
*Advice on safe handling:
Work under hood.
*Hygiene measures:
Immediately change contaminated clothing.
Apply preventive skin protection.
Wash hands and face after working with substance.
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Keep in a well-ventilated place.
Keep locked up or in an area accessible only to qualified or authorized persons.
Light sensitive.
*Storage class:
Storage class (TRGS 510): 6.1D:
Non-combustible

STABILITY and REACTIVITY of FLOCRYL NMA:
-Reactivity:
No data available
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Conditions to avoid:
no information available