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N-METHYLOLACRYLAMIDE

N-Methylolacrylamide is a chemical compound that belongs to the group of ethylene diamines. 
N-Methylolacrylamide is a special monomer with two functional groups, they are ethenyl and methylol. 
Through emulsion polymerization or solution polymerization, thermoplastic polymer may be obtained by comining N-Methylolacrylamide with many kinds of ethenyl monomer. 

CAS Number: 924-42-5
EC Number: 213-103-2
Molecular Formula: C4H7NO2
Molecular Weight: 101.1

N-Methylolacrylamide is a cross linking agent that polymerizes with acrylamide and creates cross links within the polyacrylamide gel. 
N-Methylolacrylamide is capable of creating a network rather than linear chains which helps in maintaining the firmness of gel.

N-Methylolacrylamide is a self-bred active monomer. 
In the molecular structure, N-Methylolacrylamide has a dual and active functional group conjugated with hydroxyl groups. 

N-Methylolacrylamide is very soluble in water and alcohol, and is hardly soluble in chloroform and tetrachloride. 
Carbon, N-Methylolacrylamide is easy to self-polymerize and cross-link into insoluble resin in humid air, especially under acidic conditions.

N-Methylolacrylamide is a chemical compound that belongs to the group of ethylene diamines. 
N-Methylolacrylamide has been used as a fluorescence probe for fatty acids in polyvinyl compounds, and as an electrochemical impedance spectroscopy (EIS) substrate. 

N-Methylolacrylamide also reacts with acrylamide to form polymers. 
This reaction is catalyzed by hydroxyl groups on the acrylamide molecule. 

The polymerization process is reversible, with the formation of monomers and dimers. 
The phase transition temperature ranges from -5°C to +35°C. 
Chemical stability increases with increased molecular weight, but decreases when exposed to light or air.

N-Methylolacrylamide is used in the coating and base layer of fabrics, fiber finishing, leather coating, paper coating and spray cotton or used as adhesive.

N-Methylolacrylamide is a special monomer with two functional groups, they are ethenyl and methylol. 
Through emulsion polymerization or solution polymerization, thermoplastic polymer may be obtained by comining N-Methylolacrylamide with many kinds of ethenyl monomer. 
Because there are functional groups of methylol in the branch chain, this thermoplastic polymer can self cross-link into cross-linked polymer under certain condition.

N-Methylolacrylamide because of its molecular structure contains two reactive groups, a polymerizable double bond and a condensable methylol Group, N-Methylolacrylamide therefore has the characteristics of a crosslinking agent monomer. 
The earliest synthetic method was to react acrylamide with formaldehyde to obtain crystalline N-Methylolacrylamide. 
For example, foreign scholars use paraformaldehyde and acrylamide crystals, trichloroethylene as solvent, and metal sodium colloid as catalyst to produce N-hydroxymethyl acrylamide. 

After the reaction is finished, the system naturally divides into two phases. 
When the temperature is lowered to room temperature, N-Methylolacrylamide precipitates in a large amount, and N-Methylolacrylamide is obtained, but the obtained product needs to be recrystallized with acetone or ethyl acetate.

N-Methylolacrylamide can be prepared by reaction of polyacrylamide with formaldehyde, which ameliorated water-soluble polymers used commercially include natural products, derivatives of natural products, and wholly synthetic products. 
The methylol groups of N-Methylolacrylamide are insensitive to free-radical polymerization and readily self-condense upon conventional thermal crosslinking and crosslinking reaction with carboxyl groups of acrylic pressure-sensitive adhesives (PSA). 

N-Methylolacrylamide acrylamide shows the positive influence on the molecular weight, which improved the molecular weight by about 5%. The poly-dispersion of molecular weight of synthesized solvent-borne PSA acrylics was almost on the same level. 
The monomer N-Methylolacrylamide with crosslinking properties has a practical importance as a second crosslinker agent for the production of self-adhesive acrylic pressure-sensitive adhesives with post-crosslinking effect at high temperatures.

N-Methylolacrylamide is a colorless liquid. 
N-Methylolacrylamide produces post-crosslinking site in polymers. 
N-Methylolacrylamide complies with TSCA regulation.

N-Methylolacrylamide 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.
N-Methylolacrylamide is used in formulation or re-packing, at industrial sites and in manufacturing.

N-Methylolacrylamide appears as a colorless or yellow aqueous solution.
N-Methylolacrylamide is a bi-functional monomer with reactive vinyl and hydroxyethyl groups. 

Thermoplastic polymers can be formed by copolymerization of N-methylol-acrylamide with a variety of vinyl monomers by emulsion, solution and suspension techniques. 
The resulting products, which have pendant hydroxyethyl groups, can undergo cross-linking under moderate conditions, permitting conversion of thermoplastic backbone polymers to thermoset materials at the point of use in the absence of an external cross-linking agent. 

Conversely, the hydroxyethyl group can be reacted with a substrate like cellulose and subsequently cross-linked by free-radical polymerization
The uses of N-Methylolacrylamide range from adhesives and binders in papermaking and textiles to a variety of surface coatings and resins for varnishes, films and sizing agents. 
N-Methylolacrylamide can be used in wet-strength and dry-strength agents for paper, in textile finishing agents for crease resistance, in antistatic agents, in dispersing agents, in cross-linking agents and in emulsion polymers.

Usages of N-Methylolacrylamide:
N-Methylolacrylamide has a double bond conjugated with a carbonyl group and a highly reactive methylol group. 
N-Methylolacrylamide is a widely used cross-linking monomer for fiber modification, resin processing, adhesives and paper, leather, metal surfaces The treatment agent can also be used as a soil amendment. 

N-Methylolacrylamide can be used as a cross-linking agent widely used in fiber modified resins, processing dyes, plastic adhesives to make emulsion adhesives and thermosetting acrylic coatings; copolymers with acrylamide can be used as waterproofing agents, flame retardants, etc. 
Condensation with cotton fibers can prevent fabric wrinkles and improve stain resistance.

Uses of N-Methylolacrylamide:
N-Methylolacrylamide molecule has double bond conjugated with carbonyl and reactive hydroxymethyl, N-Methylolacrylamide 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. 
The oral LD50 of male mice was 420mg/kg.

N-Methylolacrylamide can be used as crosslinking agent, widely used in fiber modification resin, processing dye, plastic adhesive, soil stabilizer, etc.
N-Methylolacrylamide is organic synthetic monomer can be used to prepare a variety of copolymers.

N-Methylolacrylamide is a bifunctional monomer with reactive vinyl and hydroxymethyl groups. 
Thermoplastic polymers can be formed by copolymerization of N-Methylolacrylamide with a variety of vinyl monomers by emulsion, solution and suspension techniques. 

The resulting products, which have pendant hydroxymethyl groups, can undergo cross-linking under moderate conditions, permitting conversion of thermoplastic backbone polymers to thermoset materials at the point of use in the absence of an external cross-linking agent. 
Conversely, the hydroxymethyl group can be reacted with a substrate like cellulose and subsequently cross-linked by free-radical polymerization.

The uses of N-Methylolacrylamide range from adhesives and binders in papermaking and textiles to a variety of surface coatings and resins for varnishes, films and sizing agents. 
N-Methylolacrylamide can be used in wet-strength and dry-strength agents for paper, in textile finishing agents for crease resistance, in antistatic agents, in dispersing agents, in cross-linking agents and in emulsion polymers.

N-Methylolacrylamide is used in adhesives, binders, surface coatings, and resins.
N-Methylolacrylamide is used as a starch modifier.
N-Methylolacrylamide is proposed for use in sunscreen preparations.

N-Methylolacrylamide are used in the formulation of grouting materials. 
Acrylamide reacts readily with formaldehyde to form N-Methylolacrylamide.

Other Uses:
Home maintenance - lubricant

Uses at industrial sites:
N-Methylolacrylamide is used in the following products: polymers. 
N-Methylolacrylamide has an industrial use resulting in manufacture of another substance (use of intermediates). 

N-Methylolacrylamide is used in the following areas: agriculture, forestry and fishing and formulation of mixtures and/or re-packaging. 
N-Methylolacrylamide is used for the manufacture of: chemicals and textile, leather or fur. 
Release to the environment of N-Methylolacrylamide 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.

Industry Uses:
Monomers
Paint additives and coating additives not described by other categories

Industrial Processes with risk of exposure:
Painting (Pigments, Binders, and Biocides)
Working with Glues and Adhesives

Applications of N-Methylolacrylamide:
N-Methylolacrylamide has been used in gel preparation.
N-Methylolacrylamide has also been used as a test compound for studying the biochemical isolation of insoluble Tau in transgenic mouse models of tauopathy by examining the two main isolation methods sarkosyl and formic acid extraction.
Cross-linking agent for preparation of polyacrylamides.

N-Methylolacrylamide has two active groups in N-Methylolacrylamide molecular structure, polymerizable double bonds and condensable methylol groups, so N-Methylolacrylamide has the characteristics of crosslinking agent monomer and is widely used in the fields of fiber modification, resin processing, coatings, plastics.
Such as adhesives, oilfield additives and soil conditioners.

In addition, N-Methylolacrylamide can be polymerized with various monomers in an aqueous system to prepare a polymer with excellent performance, which is now a widely used fine chemical.
Foreign research and application of this technology is relatively mature, domestic application is still very limited, many applications still need more research and development, N-Methylolacrylamide can also play a greater potential and value.

Production of N-Methylolacrylamide:
Acrylamide reacts readily with formaldehyde to form N-Methylolacrylamide. 
Information available in 1991 indicated that N-Methylolacrylamide was produced by two companies in Japan and one each in the Netherlands, the United Kingdom and the USA. 
In Japan, about 900 tonnes were produced as powder and 250 tonnes as water solution in 1992.

Preparation of N-Methylolacrylamide:
Acrylamide is added to the reaction kettle filled with solvent acetone, raise the temperature to 42~45 ℃
Add the catalyst sodium methoxide, adjust the pH value of the reaction solution to 8.88

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
Phthalic acid was added to adjust the pH of the reaction solution to 7.2
The reaction solution was cooled, crystallized and filtered to obtain the finished N-Methylolacrylamide.

Occurrence of N-Methylolacrylamide:

Natural occurrence:
N-Methylolacrylamide is not known to occur as a natural product.

Occupational exposure:
No data on human exposure to N-Methylolacrylamide were available to the Working Group.

The National Occupational Exposure Survey conducted by the National Institute for Occupational Safety and Health between 1981 and 1983 indicated that 20 700 US employees were potentially exposed to a product containing N-methylolalcrylamide. 
The estimate is based on a survey of US companies and did not involve measurements of actual exposures.

Regulations and guidelines:
There are no reported occupational standards or guidelines for N-Methylolacrylamide. 
The US Food and Drug Administration (1993) permits use of polymers of N-Methylolacrylamide in products in contact with food.

General Manufacturing Information of N-Methylolacrylamide:

Industry Processing Sectors:
All Other Chemical Product and Preparation Manufacturing
Plastics Material and Resin Manufacturing

Chemical and Physical Properties of N-Methylolacrylamide:
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, N-Methylolacrylamide will rapidly polymerize into insoluble resin

White crystalline solid
Melting-point: 74–75 °C
Spectroscopy data: Infrared [10698], ultraviolet and nuclear magnetic resonance spectral data have been reported.

Solubility: 
Soluble in water (188 g/100 ml at 20 °C), methanol (149 g/100 ml at 30 °C), 90% ethanol (116 g/100 ml at 30 °C), isopropanol (53 g/100 ml at 30 °C) and n-butanol (42 g/100 ml at 30 °C)

Stability: 
Aqueous solutions are highly reactive. 
Upon heating in the presence of acids, they are rapidly polymerized to infusible resins. 
The stability of solutions is dependent mainly upon oxygen level, contaminants, storage temperature and pH.

Conversion factor: 
mg/m3 = 4.13×ppma

Technical products and impurities of N-Methylolacrylamide:

N-Methylolacrylamide is available commercially as a 48% aqueous solution with the following specifications:
Assay, 48%
Water, 51-54% (typically, 52%)
pH, 5.5-6.5
Free formaldehyde, 1.5- < 3 wt%
Acrylamide, < 5.0 wt%
Copper, 2 ppm max.
Methylether of hydroquinone (inhibitor), 30 ppm
Specific gravity at 25 °C, 1.10

Mechanism of Action of N-Methylolacrylamide:
After a dose of 100 mg/kg of acrylamide no neurological signs of neuropathy had yet appeared, but retrograde buildup of protein label was significantly reduced for the long interval. 
To test the specificity of acrylamide on the retrograde transport defect n-hyroxymethylacrylamide was studied. 
N-Methylolacrylamide did not influence the transport.

Handling and Storage of N-Methylolacrylamide:

SMALL SPILLS AND LEAKAGE: 
If you spill this chemical, you should dampen the solid spill material with water, then transfer the dampened material to a suitable container. 
Use absorbent paper dampened with water to pick up any remaining material. 

Seal your contaminated clothing and the absorbent paper in a vapor-tight plastic bag for eventual disposal. 
Wash all contaminated surfaces with a soap and water solution. 
Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned. 

STORAGE PRECAUTIONS: 
You should protect this material from exposure to light. 
Keep N-Methylolacrylamide away from oxidizing materials and store N-Methylolacrylamide at refrigerated temperatures.

Safe Storage:
Separated from acids. 
Store only if stabilized. 
Store in an area without drain or sewer access.

Reactivity Profile of N-Methylolacrylamide:
N-Methylolacrylamide may be sensitive to prolonged exposure to light. 
Polymerization and generation of heat and flames may occur on exposure to to heat or contaminants. 
Incompatible with strong oxidizers.

Safety Information of N-Methylolacrylamide:

Signal Word:
Danger

Hazard Statements:
H301 - H312 - H340 - H350 - H361fd - H372

Precautionary Statements:
P202 - P260 - P264 - P280 - P301 + P310 - P302 + P352 + P312

Hazard Classifications:
Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Carc. 1B - Muta. 1B - Repr. 2 - STOT RE 1 Oral

Target Organs:
Peripheral nervous system

Storage Class Code:
6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK:
WGK 3

Personal Protective Equipment:
Dust mask type N95 (US), Eyeshields, Gloves

First Aid Measures of N-Methylolacrylamide:

EYES: 
First check the victim for contact lenses and remove if present. 
Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. 

Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. 
IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop. 

SKIN: 
IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing. 
Gently wash all affected skin areas thoroughly with soap and water. 

IMMEDIATELY call a hospital or poison control center even if no symptoms (such as redness or irritation) develop. 
IMMEDIATELY transport the victim to a hospital for treatment after washing the affected areas. 

INHALATION: 
IMMEDIATELY leave the contaminated area; take deep breaths of fresh air. 
IMMEDIATELY call a physician and be prepared to transport the victim to a hospital even if no symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop.

Provide proper respiratory protection to rescuers entering an unknown atmosphere. 
Whenever possible, Self-Contained Breathing Apparatus (SCBA) should be used.
If not available, use a level of protection greater than or equal to that advised under Protective Clothing. 

INGESTION: 
DO NOT INDUCE VOMITING. 
If the victim is conscious and not convulsing, give 1 or 2 glasses of water to dilute the chemical and IMMEDIATELY call a hospital or poison control center. 

Be prepared to transport the victim to a hospital if advised by a physician. 
If the victim is convulsing or unconscious, do not give anything by mouth, ensure that the victim's airway is open and lay the victim on his/her side with the head lower than the body. 

DO NOT INDUCE VOMITING. 
IMMEDIATELY transport the victim to a hospital. 

OTHER: 
Since this chemical is a known or suspected carcinogen you should contact a physician for advice regarding the possible long term health effects and potential recommendation for medical monitoring. 
Recommendations from the physician will depend upon the specific compound, N-Methylolacrylamide, physical and toxicity properties, the exposure level, length of exposure, and the route of exposure.

Accidental Release Measures of N-Methylolacrylamide:

Spillage Disposal of N-Methylolacrylamide:

Personal protection:
Particulate filter respirator adapted to the airborne concentration of N-Methylolacrylamide. 
Do NOT let this chemical enter the environment. 

Sweep spilled substance into covered containers. 
Then store and dispose of according to local regulations.

Disposal Methods of N-Methylolacrylamide:
At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. 
Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.

Identifiers of N-Methylolacrylamide:
Substance: N-Methylolacrylamide
CAS: 924-42-5
EC number: 213-103-2
Min. purity / concentration: 99%
Color: Colorless, White, Yellow
Appearance: Granules
Grades: Technical
IUPAC name: N-(hydroxymethyl)-2-Propenamide
Molecular formula: C4H7NO2

EC / List no.: 213-103-2
CAS no.: 924-42-5
Mol. formula: C4H7NO2

CAS No.: 924-42-5
Chemical Name: N-Methylolacrylamide
CBNumber: CB3182194
Molecular Formula: C4H7NO2
Molecular Weight: 101.1
MDL Number: MFCD00004597
MOL File: 924-42-5.mol

CAS Number: 924-42-5
Name: N-(Hydroxymethyl)acrylamide
Synonym: N-Methylolacrylamide;2-Propenamide, N-(hydroxymethyl)-;
Melting Point: 74-75ºC
Boiling Point: 318.1ºC at 760mmHg
Flash Point: 146.2ºC
Molecular Formula: C4H7NO2
Molecular Weight: 101.10400
Density: 1.074

Synonym(s): Bis-acrylamide
Linear Formula: (H2C=CHCONH)2CH2
CAS Number: 110-26-9
Molecular Weight: 154.17
EC Number: 203-750-9
MDL number: MFCD00008625
PubChem Substance ID: 24848761
Flavis number: 7.107
NACRES: NB.22

Properties of N-Methylolacrylamide:
Vapor density: 5.31 (vs air)
Quality Level: 100
Assay: 99%
Form: powder
mp: >300 °C (lit.)
Solubility: water: soluble 20 g/L at 20 °C
Storage temp.: 2-8°C
SMILES string: C=CC(=O)NCNC(=O)C=C
InChI: 1S/C7H10N2O2/c1-3-6(10)8-5-9-7(11)4-2/h3-4H,1-2,5H2,(H,8,10)(H,9,11)
InChI key: ZIUHHBKFKCYYJD-UHFFFAOYSA-N

Melting point: 74-75°C
Boiling point: 277°C(lit.)
Density: 1.082 g/mL at 20 °C
vapor pressure: 31 hPa (25 °C)
refractive index: n20/D 1.413
Flash point: 100°C
storage temp.: Store at <= 20°C.
solubility: Chloroform (Slightly), Methanol (Slightly)
pka: 13.25±0.10(Predicted)
form: Solid
color: White to Off-White
Specific Gravity: 1.074
PH: 6.0-7.0 (H2O, 20°C)
Water Solubility: <0.1 g/100 mL at 20.5 ºC
BRN: 506646
Stability: Light Sensitive, Moisture Sensitive
InChIKey: CNCOEDDPFOAUMB-UHFFFAOYSA-N
LogP: -1.81 at 20℃ and pH7

CAS Number: 924-42-5
Sensitivity: Sensitive to light; Heat sensitive; Sensitive to humidity
Solubility: Soluble in alcohol and water, water solubility 1880 g / L 20 ° C
Storage Temp: Store at 2-8°C,Protected from light
MDL number: MFCD00004597
Density: 1.074
Brand: Aladdin
Code Formula: C4H7NO2

IUPAC Name: N-(hydroxymethyl)prop-2-enamide
INCHI: InChI=1S/C4H7NO2/c1-2-4(7)5-3-6/h2,6H,1,3H2,(H,5,7)
InChi Key: CNCOEDDPFOAUMB-UHFFFAOYSA-N
Canonical SMILES: C=CC(=O)NCO
PubChem CID: 13543
Molecular Weight: 101.1
Reaxy-Rn: 506646
Refractive index: 1.413
Boil point(°C): 277°C
Melt point(°C): 76°C

Molecular Weight: 101.10
XLogP3-AA: -0.5
Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 2
Exact Mass: 101.047678466
Monoisotopic Mass: 101.047678466
Topological Polar Surface Area: 49.3 Ų
Heavy Atom Count: 7
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

Names of N-Methylolacrylamide:

Regulatory process names:
2-Propenamide, N-(hydroxymethyl)-
<I>N</I>-(hydroxymethyl)acrylamide; methylolacrylamide; [NMA]
Acrylamide, N-(hydroxymethyl)-
Hydroxymethylacrylamide
Methylolacrylamide
Monomethylolacrylamide
N-(Hydroxymethyl)-2-propenamide
N-(hydroxymethyl)acrylamide
N-(Hydroxymethyl)acrylamide
N-(hydroxymethyl)acrylamide
N-(hydroxymethyl)acrylamide; methylolacrylamide; [NMA]
N-Methanolacrylamide
N-Methylolacrylamide
N-methylolacrylamide
Uramine T 80

Translated names:
<I>N</I>-(hidroksimetil)akrilamid; metilolakrilamid; [NMA] (hr)
<I>N</I>-(hidroksimetil)akrilamid; metilolakrilamid; [NMA] (sl)
<I>N</I>-(hidroksimetil)akrilamidas metilolakrilamidas; [NMA] (lt)
<I>N</I>-(hidroksimetil)akrilamīds; metiloakrilamīds; [NMA] (lv)
<I>N</I>-(Hidroximetil)acrilamida; metilolacrilamida; [NMA] (es)
<I>N</I>-(hidroximetil)acrilamida; metilolacrilamida; [NMA] (pt)
<I>N</I>-(hidroximetil)acrilamidă; metilolacrilamidă; [NMA] (ro)
<I>N</I>-(hidroximetil)akrilamid; metilolakrilamid; [NMA] (hu)
<I>N</I>-(hydroksimetyyli)akryyliamidi; metyloliakryyliamidi; [NMA] (fi)
<I>N</I>-(hydroksymetylo)akrylamid; metylolakrylamid; [NMA] (pl)
<I>N</I>-(hydroximetyl)akrylamid; metylolakrylamid; [NMA] (sv)
<I>N</I>-(hydroxymethyl)acrylamid; methylolacrylamid; [NMA] (da)
<I>N</I>-(hydroxymethyl)acrylamid; Methylolacrylamid; [NMA] (de)
<I>N</I>-(hydroxymethyl)acrylamide; methylolacrylamide; [NMA] (nl)
<I>N</I>-(hydroxymethyl)akrylamid; methylolakrylamid; [NMA] (cs)
<I>N</I>-(hydroxymetyl)akrylamid metylolakrylamid; [NMA] (sk)
<I>N</I>-(hydroxyméthyl)acrylamide; méthylolacrylamide; [NMA] (fr)
<I>N</I>-(hüdroksümetüül)akrüülamiid; metüloolakrüülamiid; [NMA] (et)
<I>N</I>-(idrossimetil)acrilammide; metilolacrilammide; [NMA] (it)
<I>N</I>-(idrossimetil)akrilammid; metilolakrilammid; [NMA] (mt)
<I>N</I>-(υδροξυμεθυλ)ακρυλαμίδιο· μεθυλολακρυλαμίδιο· [NMA] (el)
<I>N</I>-(хидроксиметил)акрилмид; метилолакриламид; [NMA] (bg)

CAS name:
2-Propenamide, N-(hydroxymethyl)-

IUPAC name:
2-Propenamide,N-(hydroxymethyl)-
AMOL
N-(Hydroxymethyl)acrylamide
N-(hydroxymethyl)acrylamide
n-(hydroxymethyl)acrylamide
N-(Hydroxymethyl)acrylamide
N-(hydroxymethyl)acrylamide
N-(hydroxymethyl)acrylamide (NMA)
N-(hydroxymethyl)prop-2-enamide
N-Methylol acrylamide; (48% in water)
N-Methylolacrylamide
N-Methylolacrylamide
NMA

Trade names:
Cylink NMA Monomer, 48% Aqueous, inhibited
FLOCRYL NMA
Flocryl NMA
N-Methylol acrylamide; (48% in water)

Other identifiers:
160278-55-7
160278-55-7
176598-18-8
176598-18-8
194091-52-6
194091-52-6
211862-48-5
211862-48-5
211862-50-9
211862-50-9
616-230-00-5
90456-67-0
90456-67-0
924-42-5

Synonyms of N-Methylolacrylamide:
N-(HYDROXYMETHYL)ACRYLAMIDE
N-Methylolacrylamide
924-42-5
Methylolacrylamide
N-Methylol Acrylamide
N-Methanolacrylamide
Monomethylolacrylamide
2-Propenamide, N-(hydroxymethyl)-
Acrylamide, N-(hydroxymethyl)-
N-(hydroxymethyl)prop-2-enamide
N-Hydroxymethyl acrylamide
Uramine T 80
N-(Hydroxymethyl)-2-propenamide
Hydroxymethylacrylamide
NCI-C60333
N-MAM
NSC 553
Yuramin T 80
W8W68JL80Q
CHEBI:82492
NSC-553
MFCD00004597
N-Methyloacrylamide
CCRIS 2380
HSDB 4361
NM-AMD
EINECS 213-103-2
BRN 0506646
UNII-W8W68JL80Q
AI3-25447
ROCAGIL BT
EC 213-103-2
N-(hydroxymethyl) acrylamide
SCHEMBL25806
METHYLOLACRYLAMIDE, N-
NSC553
CHEMBL1892361
DTXSID3020885
N-METHYLOLACRYLAMIDE [IARC]
ZINC1555606
AKOS006222324
CS-W013710
NCGC00163845-01
NCGC00163845-02
BS-17859
N-(HYDROXYMETHYL)ACRYLAMIDE [HSDB]
FT-0720637
M0574
C19456
E78933
EN300-7474805
A844235
W-100289
Q26840808
N-(Hydroxymethyl)acrylamide 100 microg/mL in Acetonitrile
(1Z)-N-(Hydroxymethyl)-2-propenimidic acid [ACD/IUPAC Name]
(1Z)-N-(Hydroxymethyl)-2-propenimidsäure [German] [ACD/IUPAC Name]
213-103-2 [EINECS]
2-Propenamide, N-(hydroxymethyl)- [ACD/Index Name]
2-Propenimidic acid, N-(hydroxymethyl)-, (1Z)- [ACD/Index Name]
924-42-5 [RN]
Acide (1Z)-N-(hydroxyméthyl)-2-propénimidique [French] [ACD/IUPAC Name]
N-(Hydroxymethyl)acrylamid [German] [ACD/IUPAC Name]
N-(Hydroxymethyl)acrylamide [ACD/IUPAC Name]
N-(Hydroxyméthyl)acrylamide [French] [ACD/IUPAC Name]
N-(hydroxymethyl)prop-2-enamide
N-hydroxymethylacrylamide
n-methylol acrylamide
N-Methylolacrylamide
[924-42-5] [RN]
000924-42-5 [RN]
160278-55-7 [RN]
176598-18-8 [RN]
194091-52-6 [RN]
2-Propenamide, N- (hydroxymethyl)-
90456-67-0 [RN]
Acrylamide, N- (hydroxymethyl)-
acrylamide, N-(hydroxymethyl)-
ACRYLAMIDE, N-HYDROXYMETHYL
AS3600000
BS-17859
EINECS 213-103-2
Hydroxymethylacrylamide
-methylolacrylamide
Methylolacrylamide
MONOMETHYLOLACRYLAMIDE
N
N-(Hydroxymethyl)-2-propenamid
N-(Hydroxymethyl)-2-propenamide
N-(Hydroxymethyl)-acrylamid
N-(Hydroxymethyl)acrylamide (en)
n-(hydroxymethyl)acrylamide, ???
N-(Hydroxymethyl)acrylamidemissing
NCGC00163845-01
NCGC00163845-02
N-hydroxymethyl acrylamide
N-MAM
NM-AMD
N-methanolacrylamide
N-methyloacrylamide
Uramine T 80
uramine t 80.
Yuramin T 80
 

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