Conditions | Yield |
---|---|
With amorphous Cu-Ti alloy; hydrogen fluoride Product distribution; other Cu alloys or Cu metal, absence HF; | 100% |
With water; aluminum oxide; Ru(OH)x at 119.85℃; for 24h; | 100% |
With water; copper chromite, reduced, supported in stainless steel wire socks at 64 - 96℃; under 637.564 Torr; Heating / reflux; | 100% |
Conditions | Yield |
---|---|
With water at 0 - 4℃; for 7.5h; culture broth containing cells of Pseudomonas chlororaphis, strain B23; | A 99% B 0.7% |
With water; copper oxide, reduced, supported in stainless steel wire socks at 135 - 158℃; under 3760.13 Torr; Heating / reflux; |
Conditions | Yield |
---|---|
With deglycase DJ-1 at 70℃; Reagent/catalyst; Temperature; Enzymatic reaction; | 98% |
Conditions | Yield |
---|---|
With choline chloride * 2ZnCl2; hydroxylamine hydrochloride at 80℃; for 15h; Green chemistry; | 91% |
With hydroxylamine In water at 110℃; for 12h; | 76% |
With hydroxylamine In water at 110℃; for 12h; | 76% |
acrylonitrile
isobutene
A
N-tert-Butylacrylamide
B
2-acrylamido-2-methylpropanesulfonic acid
C
2-propenamide
Conditions | Yield |
---|---|
With sulfuric acid at 20℃; for 2h; | A n/a B 87% C n/a |
2-(2-aminobenzoyl)benzoic acid
water
acryloyl chloride
B
2-propenamide
Conditions | Yield |
---|---|
With hydrogenchloride; sodium hydroxide In ethanol | A 86% B n/a |
Conditions | Yield |
---|---|
In acetone at 20℃; for 2h; Inert atmosphere; Schlenk technique; | A 85% B 86% |
3-(morpholin-4-yl)propionamide
acetic anhydride
A
4-acetylmorpholine
B
2-propenamide
Conditions | Yield |
---|---|
Stage #1: 3-(morpholin-4-yl)propionamide; acetic anhydride In toluene at 20 - 80℃; for 2h; Inert atmosphere; Stage #2: With 2,6-di-tert-butyl-4-methyl-phenol; triethylamine Reagent/catalyst; Reflux; | A 84% B 86% |
Conditions | Yield |
---|---|
In ethanol; water | 83% |
Conditions | Yield |
---|---|
With ammonia; Ti-0720 (Engelhard) catalyst In water at 200 - 250℃; for 37h; Product distribution / selectivity; | A n/a B 75% C n/a |
titanium catalyst In water at 180℃; for 37h; Product distribution / selectivity; | A 1.5% B 65% C n/a |
titanium catalyst In water at 180℃; for 37h; Product distribution / selectivity; | A 1.5% B 65% C n/a |
Conditions | Yield |
---|---|
With ammonia; Ti-0720 In water at 200 - 250℃; Product distribution / selectivity; | A n/a B 75% |
silica-alumina catalyst (Si/Al T-869) In water at 240℃; for 37h; Product distribution / selectivity; |
Conditions | Yield |
---|---|
With Escherichia coli deglycase YhbO at 70℃; Reagent/catalyst; Temperature; Enzymatic reaction; | 74% |
Conditions | Yield |
---|---|
With peptidase PfpI from Pyrococcus furiosus In aq. phosphate buffer at 95℃; pH=7.5; Reagent/catalyst; Enzymatic reaction; | 70% |
Conditions | Yield |
---|---|
With peptidase PfpI from Pyrococcus furiosus In aq. phosphate buffer at 95℃; pH=7.5; Reagent/catalyst; Enzymatic reaction; | 70% |
Conditions | Yield |
---|---|
With sodium bicarbonate; sodium carbonate; tetra(n-butyl)ammonium hydrogen sulfate In dichloromethane | 69% |
acrylonitrile
acetone
A
N-(1,1-dimethyl-3-oxobutyl)acrylamide
B
2-propenamide
Conditions | Yield |
---|---|
sulfuric acid at 58℃; for 4.5h; | A 63% B 37% |
Conditions | Yield |
---|---|
With copper diacetate; palladium diacetate In water at 120℃; for 1h; Reagent/catalyst; Schlenk technique; Green chemistry; | A 61% B 53% |
Conditions | Yield |
---|---|
dmap In dichloromethane | 59% |
Conditions | Yield |
---|---|
In methanol; dichloromethane | A 57% B n/a |
Conditions | Yield |
---|---|
With dihydrogen peroxide; crotonamide In methanol; water at 39.84℃; for 5h; Reagent/catalyst; | A 51% B 17% |
With dihydrogen peroxide; magnesium oxide In methanol; water at 39.84℃; for 5h; Reagent/catalyst; | A 6% B 21% |
Conditions | Yield |
---|---|
With C18H57O3P6Ru2(1+)*C6H5O(1-)*C6H6O; water at 80℃; for 20h; Catalytic behavior; Sealed tube; Inert atmosphere; Schlenk technique; | A 46% B 27% |
Conditions | Yield |
---|---|
With sulfuric acid; hydroquinone at 10 - 40℃; for 6h; Ritter reaction; | A n/a B n/a C 34.3% |
Conditions | Yield |
---|---|
With diphenylphosphoranyl azide; triethylamine In N-methyl-acetamide; THF-n-hexane; N,N-dimethyl-formamide | 25% |
acrylonitrile
A
3-(4-Benzyloxy-2,2,6,6-tetramethyl-piperidin-1-yloxy)-propionamide
B
2-propenamide
Conditions | Yield |
---|---|
With 4-(benzyloxy)-1-hydroxy-2,2,6,6-tetramethylpiperidine In dichloromethane at 50℃; for 65h; | A 19% B 22% |
Conditions | Yield |
---|---|
With sodium carbonate at 150℃; under 5 Torr; | |
In water Product distribution / selectivity; | |
With silica gel at 300℃; Inert atmosphere; Autoclave; | 99 %Spectr. |
(3-methoxypropyl)amide
2-propenamide
Conditions | Yield |
---|---|
With calcium oxide at 260℃; unter vermindertem Druck; | |
With methanol; N-Phenyl-2-naphthylamine; titanium(IV) oxide at 300 - 365℃; | |
With methanol; lithium phosphate; N-Phenyl-2-naphthylamine at 300 - 365℃; |
Conditions | Yield |
---|---|
With ammonia |
Conditions | Yield |
---|---|
With carbon monoxide; ammonia; tetracarbonyl nickel |
Conditions | Yield |
---|---|
With ammonia; benzene | |
With ammonia | |
With ammonia In diethyl ether | |
With triethanolamine In 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran | |
With sodium bicarbonate; triethylamine In dichloromethane |
2-propenamide
2,3-dibromopropionamide
Conditions | Yield |
---|---|
With bromine In methanol for 0.5h; Reflux; | 100% |
With bromine In methanol at 65℃; for 2h; | 99% |
With bromine In methanol at 65℃; for 2h; Reflux; | 99% |
diethoxyacetaldehyde
2-propenamide
N-(hydroxy-1 diethoxy-2,2) ethyl acrylamide
Conditions | Yield |
---|---|
With 4-methoxy-phenol at 70℃; for 2h; | 100% |
Conditions | Yield |
---|---|
With hydrogen; palladium(II) complex of ferrocenylamine sulfide (3) In acetone under 4137.2 Torr; for 0.25h; | 100% |
With hydrogen In ethanol at 20℃; under 760.051 Torr; for 1h; chemoselective reaction; | 99% |
With formic acid In methanol; water at 100℃; for 12h; Green chemistry; chemoselective reaction; | 91% |
2-propenamide
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 50℃; for 21h; Addition; Michael addition; | 100% |
Conditions | Yield |
---|---|
Stage #1: 3-(acryloyloxy)-2-hydroxypropyl methacrylate; 3-(acryloyloxy)-2-hydroxypropyl methacrylate (cross-linked); mixture of; 2-propenamide; acrylic acid In water for 0.0333333h; pH=7.3; sodium phosphate buffer; sonication; Stage #2: With bis(2-ethylhexyl) sulfosuccinate; BRIJ 30 In hexane; water at 20℃; for 0.333333h; sonication; Stage #3: With ammonium peroxydisulfate; N,N,N,N,-tetramethylethylenediamine In hexane; water at 20℃; for 12h; | 100% |
Conditions | Yield |
---|---|
Stage #1: glycerol-1,3-dimethacrylate; 2-propenamide In water for 0.116667h; pH=7.3; sodium phosphate buffer; Sonication; Stage #2: With bis(2-ethylhexyl) sulfosuccinate; BRIJ 30 In hexane; water at 20℃; for 0.166667h; Stage #3: With ammonium peroxydisulfate; N,N,N,N,-tetramethylethylenediamine In hexane; water at 20℃; | 100% |
Stage #1: glycerol-1,3-dimethacrylate; 2-propenamide In water for 0.2h; pH=7.3; sodium phosphate buffer; Sonication; Stage #2: With bis(2-ethylhexyl) sulfosuccinate; BRIJ 30 In hexane; water at 20℃; for 0.166667h; Stage #3: With ammonium peroxydisulfate; N,N,N,N,-tetramethylethylenediamine In hexane; water at 20℃; | 100% |
Stage #1: glycerol-1,3-dimethacrylate; 2-propenamide With iron oxide In water for 0.283333h; pH=7.3; sodium phosphate buffer; Sonication; Stage #2: With bis(2-ethylhexyl) sulfosuccinate; BRIJ 30 In hexane; water at 20℃; for 0.166667h; Stage #3: With ammonium peroxydisulfate; N,N,N,N,-tetramethylethylenediamine In hexane; water at 20℃; | |
Stage #1: glycerol-1,3-dimethacrylate; 2-propenamide With Photofrin In water for 0.2h; pH=7.3; sodium phosphate buffer; Sonication; Stage #2: With bis(2-ethylhexyl) sulfosuccinate; BRIJ 30 In hexane; water at 20℃; for 0.166667h; Stage #3: With ammonium peroxydisulfate; N,N,N,N,-tetramethylethylenediamine In hexane; water at 20℃; |
Conditions | Yield |
---|---|
Stage #1: N-acryloyl-1,3-diaminopropane hydrochloride; glycerol-1,3-dimethacrylate; 2-propenamide In water for 0.166667h; pH=7.3; sodium phosphate buffer; Sonication; Stage #2: With bis(2-ethylhexyl) sulfosuccinate; BRIJ 30 In hexane; water at 20℃; for 0.166667h; Stage #3: With ammonium peroxydisulfate; N,N,N,N,-tetramethylethylenediamine In hexane; water | 100% |
2-propenamide
Conditions | Yield |
---|---|
Stage #1: glycerol(bis)methacrylate; glycerol(bis)methacrylate (cross-linked); mixture of; 2-propenamide In water for 0.116667h; pH=7.3; sodium phosphate buffer; Sonication; Stage #2: With bis(2-ethylhexyl) sulfosuccinate; BRIJ 30 In hexane; water at 20℃; for 0.166667h; Stage #3: With ammonium peroxydisulfate; N,N,N,N,-tetramethylethylenediamine In hexane; water at 20℃; | 100% |
(3-fluorophenyl)methanamine
2-propenamide
3-(3-fluorobenzylamino)propionamide
Conditions | Yield |
---|---|
In ethanol at 20℃; for 24h; | 100% |
Conditions | Yield |
---|---|
With Iron(III) nitrate nonahydrate In toluene for 12h; Reflux; | 100% |
2-acrylamido-2-methylpropanesulfonic acid
2-propenamide
polymer, Mw 61 kDa, sulfur content 6.97%, 2-acrylamido-2-methylpropanesulfonic acid units content 22.0 mol%; monomer(s): acrylamide; 2-acrylamido-2-methylpropanesulfonic acid
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile) In ethanol at 50℃; for 24h; | 99.8% |
2-acrylamido-2-methylpropanesulfonic acid
2-propenamide
polymer, Mw 36 kDa, sulfur content 6.16%, 2-acrylamido-2-methylpropanesulfonic acid units content 18.5 mol%; monomer(s): acrylamide; 2-acrylamido-2-methylpropanesulfonic acid
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile) In ethanol at 50℃; for 24h; | 99.8% |
2-acrylamido-2-methylpropanesulfonic acid
2-propenamide
polymer, Mw 19 kDa, sulfur content 6.18%, 2-acrylamido-2-methylpropanesulfonic acid units content 19.1 mol%; monomer(s): acrylamide; 2-acrylamido-2-methylpropanesulfonic acid
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile) In isopropyl alcohol at 50℃; for 24h; | 99.8% |
2-acrylamido-2-methylpropanesulfonic acid
2-propenamide
polymer, sulfur content 9.42%, 2-acrylamido-2-methylpropanesulfonic acid units content 37.6 mol%; monomer(s): acrylamide; 2-acrylamido-2-methylpropanesulfonic acid
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile) In ethanol at 50℃; for 24h; | 99.7% |
2-acrylamido-2-methylpropanesulfonic acid
2-propenamide
polymer, Mw 16 kDa, sulfur content 5.86%, 2-acrylamido-2-methylpropanesulfonic acid units content 17.3 mol%; monomer(s): acrylamide; 2-acrylamido-2-methylpropanesulfonic acid
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile) In ethanol at 50℃; for 24h; | 99.6% |
Conditions | Yield |
---|---|
With triethylamine; {[Pd(η5-C5H5)Fe(η5-C5H3)C(CH3)=N(C6H4CH3-4)](μ-I)}2 In 1,4-dioxane at 100℃; for 15h; | 99.3% |
With palladium diacetate; sodium dodecyl sulfate; potassium carbonate In water for 0.333333h; Heck reaction; Heating; Ultrasound radiation; stereoselective reaction; | 96% |
With triethylamine In N,N-dimethyl-formamide at 130℃; for 1h; Catalytic behavior; Heck Reaction; | 96% |
2-propenamide
Conditions | Yield |
---|---|
With potassium peroxomonosulphate In water at 60℃; | 99.3% |
2-acrylamido-2-methylpropanesulfonic acid
2-propenamide
polymer, Mw 28 kDa, sulfur content 7.16%, 2-acrylamido-2-methylpropanesulfonic acid units content 22.8 mol%; monomer(s): acrylamide; 2-acrylamido-2-methylpropanesulfonic acid
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile) In ethanol at 50℃; for 24h; | 99.2% |
Conditions | Yield |
---|---|
for 0.166667h; Michael Addition; | 99% |
copper In methanol at 20℃; for 5h; Aza-Michael Addition; | 95% |
With 1,1,3,3-tetramethylguanidinium lactate at 20℃; for 3h; aza-Michael addition; Neat (no solvent); | 95% |
Conditions | Yield |
---|---|
With nickel(II) ferrite In water at 20℃; Michael Addition; Green chemistry; | 99% |
With graphene oxide In water at 20℃; for 0.0833333h; aza-Michael addition; | 97% |
With ES-SO3H*Pyridine In tetrahydrofuran at 20℃; for 0.5h; Aza-Michael condensation; solid phase reaction; | 95% |
2-propenamide
phosphonic acid diethyl ester
diethyl 3-amino-3-oxopropylphosphonate
Conditions | Yield |
---|---|
With C26H53N4NdSi4 at 20℃; for 0.0833333h; Inert atmosphere; | 99% |
With Hexamethylphosphorous triamide In acetonitrile at 20℃; for 1h; Pudovik Reaction; | 94% |
With 1-ethyl-2,2,4,4,4-pentakis(dimethylamino)-2λ5,4λ5-catenadi(phosphazene) In acetonitrile at 50℃; for 1h; Anti-Markovnikov addition; | 85% |
With triethyl phosphite |
5-iodo-1,3-benzodioxole
2-propenamide
3-(1,3-benzodioxol-5-yl)-(2E)-propenamide
Conditions | Yield |
---|---|
With P-ph-phen*Pd(0); sodium acetate In water; N,N-dimethyl-formamide at 130℃; for 12h; | 99% |
With sodium acetate; <*>-p-C6H4-(1,10-phenanthroline)-palladium(0) In water; N,N-dimethyl-formamide at 130℃; for 12h; | 99% |
2-propenamide
Conditions | Yield |
---|---|
With potassium In ammonia at -40 - -33.5℃; Metallation; | 99% |
2-propenamide
Conditions | Yield |
---|---|
With sodium disulfite; potassium peroxomonosulphate; calcium chloride In water at 50℃; for 2h; pH=9; Product distribution; Kinetics; Further Variations:; Reagents; | 99% |
Thiazole-2-carbaldehyde
2-propenamide
Conditions | Yield |
---|---|
With 1,4-diaza-bicyclo[2.2.2]octane In 1,4-dioxane; water at 20℃; for 12h; Baylis-Hillman reaction; | 99% |
Conditions | Yield |
---|---|
With 2Br(1-)*C46H48N4O2(2+); palladium diacetate; sodium carbonate In N,N-dimethyl acetamide at 140℃; for 10h; Heck reaction; Inert atmosphere; stereoselective reaction; | 99% |
With tetrabutylammomium bromide; triethylamine In water; N,N-dimethyl-formamide at 110℃; for 4h; Heck Reaction; Green chemistry; | 94% |
With sodium acetate; {Pd[P(o-C6H4CH3)2(C6H4CH2)][OCOCH3]}2 In N,N-dimethyl acetamide at 140℃; for 20h; Heck arylation; | 62% |
Conditions | Yield |
---|---|
for 0.166667h; Michael Addition; | 99% |
With nickel(II) ferrite In water at 20℃; Michael Addition; Green chemistry; | 97% |
With graphene oxide In water at 20℃; for 0.0833333h; aza-Michael addition; | 94% |
Product Name: Acrylamide (CAS NO.79-06-1)
Molecular Formula: C3H5NO
Molecular Weight: 71.08g/mol
Mol File: 79-06-1.mol
EINECS: 201-173-7
Melting Point: 82-86 °C(lit.)
Boiling point: 231.7 °C at 760 mmHg
Storage Temperature: 2-8°C
Flash Point: 79 °C
Density: 0.961 g/cm3
Refractive index: 1.460
Water Solubility: H2O: 50 mg/mL at 20 °C, clear, colorless
Sensitive: Light Sensitive
Stability: Unstable. Do not heat above 50C. Explosive. Incompatible with acids, bases, oxidizing agents, reducing agents, iron and iron salts, copper, aluminium, brass, free radical initiators. Air sensitive. Hygroscopic.
Index of Refraction: 1.433
Molar Refractivity: 19.23 cm3
Molar Volume: 73.9 cm3
Surface Tension: 31 dyne/cm
Enthalpy of Vaporization: 46.84 kJ/mol
Vapour Pressure: 0.0614 mmHg at 25°C
XLogP3-AA: -0.7
H-Bond Donor: 1
H-Bond Acceptor: 1
Structure Descriptors of Acrylamide (CAS NO.79-06-1):
IUPAC Name: prop-2-enamide
Canonical SMILES: C=CC(=O)N
InChI: InChI=1S/C3H5NO/c1-2-3(4)5/h2H,1H2,(H2,4,5)
InChIKey: HRPVXLWXLXDGHG-UHFFFAOYSA-N
Product Categories: Industrial/Fine Chemicals; Acrylamide; Reagents for Electrophoresis; Biochemistry; Water Ttreatment Chemicals; AcrylamidesGlycobiology; Electrophoresis of Glycans; Glycan Labeling and Analysis; Protein Electrophoresis; SDS-PAGE; Biochemicals; Molecular Biology; Molecular Biology Reagents
Acrylamide (CAS NO.79-06-1) is used for sewage and waste treatment and it is also used to make dyes, adhesives.
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
guinea pig | LD50 | oral | 150mg/kg (150mg/kg) | Toxicology and Applied Pharmacology. Vol. 6, Pg. 172, 1964. | |
guinea pig | LD50 | subcutaneous | 170mg/kg (170mg/kg) | BEHAVIORAL: TREMOR GASTROINTESTINAL: NAUSEA OR VOMITING BEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY) | Medicina del Lavoro. Industrial Medicine. Vol. 47, Pg. 192, 1956. |
guinea pig | LD50 | unreported | 173mg/kg (173mg/kg) | BEHAVIORAL: TREMOR BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD | Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 43(9), Pg. 38, 1978. |
mammal (species unspecified) | LD50 | oral | 100mg/kg (100mg/kg) | Kagaku to Seibutsu. Chemistry and Biology. Vol. 17, Pg. 495, 1979. | |
mammal (species unspecified) | LDLo | intravenous | 190mg/kg (190mg/kg) | Comptes Rendus Hebdomadaires des Seances, Academie des Sciences. Vol. 153, Pg. 895, 1911. | |
mouse | LD50 | intraperitoneal | 170mg/kg (170mg/kg) | Toxicology and Applied Pharmacology. Vol. 33, Pg. 142, 1975. | |
mouse | LD50 | oral | 107mg/kg (107mg/kg) | Archives of Toxicology. Vol. 47, Pg. 179, 1981. | |
mouse | LD50 | unreported | 156mg/kg (156mg/kg) | BEHAVIORAL: TREMOR BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY) | Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 43(9), Pg. 38, 1978. |
quail | LD50 | oral | 186mg/kg (186mg/kg) | PERIPHERAL NERVE AND SENSATION: FLACCID PARALYSIS WITHOUT ANESTHESIA (USUALLY NEUROMUSCULAR BLOCKAGE) BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX) BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY) | Journal of Toxicology and Environmental Health. Vol. 7, Pg. 935, 1981. |
rabbit | LD50 | oral | 150mg/kg (150mg/kg) | Toxicology and Applied Pharmacology. Vol. 6, Pg. 172, 1964. | |
rabbit | LD50 | skin | 1680uL/kg (1.68mL/kg) | BEHAVIORAL: "HALLUCINATIONS, DISTORTED PERCEPTIONS" | Acute Toxicity Data. Journal of the American College of Toxicology, Part B. Vol. 1, Pg. 115, 1990. |
rabbit | LD50 | unreported | 280mg/kg (280mg/kg) | BEHAVIORAL: TREMOR BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD | Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 43(9), Pg. 38, 1978. |
rat | LD50 | intraperitoneal | 90mg/kg (90mg/kg) | Archives des Maladies Professionnelles de Medecine du Travail et de Securite Sociale. Vol. 36, Pg. 58, 1975. | |
rat | LD50 | oral | 124mg/kg (124mg/kg) | Archives des Maladies Professionnelles de Medecine du Travail et de Securite Sociale. Vol. 36, Pg. 58, 1975. | |
rat | LD50 | skin | 400mg/kg (400mg/kg) | BLOOD: OTHER CHANGES | Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 44(10), Pg. 73, 1979. |
rat | LD50 | unreported | 208mg/kg (208mg/kg) | BEHAVIORAL: TREMOR BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY) | Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 43(9), Pg. 38, 1978. |
NTP 10th Report on Carcinogens. IARC Cancer Review: Group 2B MELAAD Medicina del Lavoro. Industrial Medicine. 47 (1956),192. ; Animal Sufficient Evidence IMEMDT IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man . 39 (1986),p. 41 . EPA Extremely Hazardous Substances List. Community Right-To-Know List. Reported in EPA TSCA Inventory.
Safety Information of Acrylamide (CAS NO.79-06-1):
Hazard Codes: T
Risk Statements: 45-46-20/21-25-36/38-43-48/23/24/25-62-48/20/21/22-22-24/25
R45:May cause cancer.
R46:May cause heritable genetic damage.
R20/21:Harmful by inhalation and in contact with skin.
R25 :Toxic if swallowed.
R36/38:Irritating to eyes and skin.
R43:May cause sensitization by skin contact.
R48:Danger of serious damage to health by prolonged exposure.
R23/24/25:Toxic by inhalation, in contact with skin and if swallowed.
R62:Risk of impaired fertility.
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed.
R22:Harmful if swallowed.
R45:May cause cancer.
Safety Statements: 53-45-24-36/37/39-26-36/37
S53:Avoid exposure - obtain special instructions before use.
S45:In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection.
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37:Wear suitable protective clothing and gloves.
RIDADR: UN 3426 6.1/PG 3
WGK Germany: 3
RTECS: AS3325000
F: 8-10
HazardClass: 6.1
PackingGroup: III
HS Code: 29241900
OSHA PEL: TWA 0.03 mg/m3 (skin)
ACGIH TLV: Animal Carcinogen, TWA 0.03 mg/m3 (skin)
DFG MAK: Animal Carcinogen, Suspected Human Carcinogen
NIOSH REL: TWA 0.3 mg/m3
DOT Classification: 6.1; Label: KEEP AWAY FROM FOOD
For occupational chemical analysis use OSHA: #21.
Acrylamide , its CAS NO. is 79-06-1, the synonyms are Optimum ; Propenamide ; Propeneamide ; Propenoic acid amide .
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