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| Name |
m-Cumenol methylcarbamate |
EINECS | N/A |
| CAS No. | 64-00-6 | Density | 1.039g/cm3 |
| PSA | 41.82000 | LogP | 2.73260 |
| Solubility | 85mg/L(30 oC) | Melting Point |
53°C |
| Formula | C11H15 N O2 | Boiling Point | 260.9°C at 760 mmHg |
| Molecular Weight | 193.246 | Flash Point | 111.6°C |
| Transport Information | N/A | Appearance | N/A |
| Safety | Poison by ingestion, skin contact, intraperitoneal, intravenous, intramuscular, and possibly other routes. A pesticide. See also CARBAMATES. When heated to decomposition it emits toxic fumes of NOx. | Risk Codes | N/A |
| Molecular Structure |
|
Hazard Symbols | N/A |
| Synonyms |
m-Cumenyl methylcarbamate;64-00-6;3-Isopropylphenyl methylcarbamate;m-Cumenol methylcarbamate;Hercules 5727;m-Isopropylphenyl methylcarbamate;Compound 10854;m-Isopropylphenyl N-methylcarbamate;Union carbide 10854;Union carbide uc-10,854;Caswell No. 512A;Hercules AC 5727;m-Isopropylphenol methylcarbamate;Carbamic acid, methyl-, m-cumenyl ester;(3-propan-2-ylphenyl) N-methylcarbamate;OMS 162;m-Isopropylphenol N-methylcarbamate;3-Isopropylphenyl N-methylcarbamate;Methylcarbamic acid m-cumenyl ester;N-Methyl m-isopropylphenyl carbamate;N-Methyl 3-isopropylphenyl carbamate;Oms-631;HER. 5727;Phenol, m-isopropyl-, methylcarbamate;ENT 25,500;AC 5727;OMS-15;UC 10854;HSDB 6376;3-Isopropylphenyl-N-methylcarbamate;N-Methyl-m-isopropylphenyl carbamate;EINECS 200-572-3;N-Methyl-3-isopropylphenyl carbamate;H 5727;H 8757;N-Methyl carbamate, m-1-propylphenyl;RCRA waste no. P202;EPA Pesticide Chemical Code 047801;Carbamic acid, N-methyl-, 3-isopropylphenyl ester;3-(1-Methylethyl)phenol methylcarbamate;3-(1-Methylethyl)phenyl methylcarbamate;BRN 2051096;m-Kumenylester kyseliny methylkarbaminove;PHENOL, 3-(1-METHYLETHYL)-, METHYLCARBAMATE;Carbamic acid, methyl-, 3-(1-methylethyl)phenyl ester;UNII-27502G8UZX;AI3-25500;DTXSID1040324;27502G8UZX;m-Kumenylester kyseliny methylkarbaminove [Czech];H-8,757;ENT 25,543;1PC;Phenol, 3-(1-methylethyl)-, methyl carbamate;Hercules AC-5727;3-isopropylphenylmethylcarbamat;Phenol, 3-(1-methylethyl)-, 1-(N-methylcarbamate);OMS 15;SCHEMBL5933261;CHEMBL2046819;DTXCID9020324;CUMENYL METHYLCARBAMATE, M-;Tox21_302006;ENT 25500;(3-propan-2-ylphenyl)n-methylcarbamate;CAS-64-00-6;NCGC00255448-01;LS-50095;Phenol, 3-(methylethyl)-, methyl carbamate;H-5727;Fenol, 3-(1-metiletil)-, 1-(n-metilcarbamato);Q6712041;PHENOL, 3-(1-METHYLETHYL)-, METHYLCARBAMATE [HSDB];Cumenol methylcarbamate, m-;(3-(1-methylethyl)phenol methylcarbamate) |
m-Cumenol methylcarbamate Chemical Properties
IUPAC: (3-Propan-2-ylphenyl) N-methylcarbamate
m-Cumenol methylcarbamate (64-00-6) is also called for 1PC ; 3-(1-Methylethyl)phenol methylcarbamate ; 3-(1-Methylethyl)phenyl methylcarbamate ; 3-Isopropylphenyl methylcarbamate ; 3-Isopropylphenyl-N-methylcarbamate ; AC 5727 ; AI3-25500 ; BRN 2051096 ; Caswell No. 512A ; Compound 10854 ; EINECS 200-572-3 ; ENT 25,500 ; EPA Pesticide Chemical Code 047801 ; N-Methyl 3-isopropylphenyl carbamate ; N-Methyl carbamate, m-1-propylphenyl ; Oms-631 ; Phenol, m-isopropyl-, methylcarbamate ; UC 10854 ; Union carbide 10854 ; Union carbide UC-10,854 ; m-Kumenylester kyseliny methylkarbaminove and so on.
Molecular Formula: C11H15NO2
Molecular Weight: 193.24
EINECS: 200-572-3
LogP: ACD/LogP: 2.51
XLogP: 2.90
ALOGPS: 2.55
ACD/LogD (pH 5.5): 2.5
ACD/LogD (pH 7.4): 2.5
ACD/BCF (pH 5.5): 47.17
ACD/BCF (pH 7.4): 47.17
ACD/KOC (pH 5.5): 549.04
ACD/KOC (pH 7.4): 549.03
H bond acceptors: 3
H bond donors: 1
Freely Rotating Bonds: 3
Index of Refraction: 1.507
Molar Refractivity: 55.37 cm3
Molar Volume: 185.9 cm3
Surface Tension: 34.8 dyne/cm
Density: 1.039 g/cm3
Flash Point: 111.6°C
Enthalpy of Vaporization: 49.86 kJ/mol
Boiling Point: 260.9°C at 760 mmHg
Vapour Pressure: 0.0119 mmHg at 25°C
The appearance of m-Cumenol methylcarbamate (64-00-6) is white solid.
The molecular structure of m-Cumenol methylcarbamate (64-00-6) :
m-Cumenol methylcarbamate Uses
m-Cumenol methylcarbamate (64-00-6) is used as an insecticide to protect cotton, fruit, vegetables and field crops.
m-Cumenol methylcarbamate Toxicity Data With Reference
| Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
|---|---|---|---|---|---|
| bird - wild | LD50 | oral | 3200ug/kg (3.2mg/kg) | Toxicology and Applied Pharmacology. Vol. 21, Pg. 315, 1972. | |
| chicken | LD50 | oral | 12mg/kg (12mg/kg) | PERIPHERAL NERVE AND SENSATION: SPASTIC PARALYSIS WITH OR WITHOUT SENSORY CHANGE BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD BEHAVIORAL: ATAXIA | Toxicology and Applied Pharmacology. Vol. 11, 49. |
| dog | LDLo | intramuscular | 13mg/kg (13mg/kg) | BEHAVIORAL: TREMOR BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD GASTROINTESTINAL: NAUSEA OR VOMITING | British Journal of Industrial Medicine. Vol. 22, Pg. 317, 1965. |
| guinea pig | LDLo | oral | 10mg/kg (10mg/kg) | Pesticide Manual. Vol. 1, Pg. 263, 1968. | |
| mouse | LD50 | intraperitoneal | 3100ug/kg (3.1mg/kg) | Journal of Agricultural and Food Chemistry. Vol. 16, Pg. 561, 1968. | |
| mouse | LD50 | intravenous | 1410ug/kg (1.41mg/kg) | U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#02085, | |
| mouse | LD50 | oral | 16mg/kg (16mg/kg) | Journal of Agricultural and Food Chemistry. Vol. 18, Pg. 793, 1970. | |
| rabbit | LD50 | skin | 40mg/kg (40mg/kg) | Farm Chemicals Handbook. Vol. -, Pg. C317, 1991. | |
| rat | LD50 | intramuscular | 14mg/kg (14mg/kg) | British Journal of Industrial Medicine. Vol. 22, Pg. 317, 1965. | |
| rat | LD50 | intraperitoneal | 14200ug/kg (14.2mg/kg) | BEHAVIORAL: GENERAL ANESTHETIC LUNGS, THORAX, OR RESPIRATION: DYSPNEA LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES | Bulletin of the World Health Organization. Vol. 44, Pg. 241, 1971. |
| rat | LD50 | intravenous | 3150ug/kg (3.15mg/kg) | British Journal of Industrial Medicine. Vol. 22, Pg. 317, 1965. | |
| rat | LD50 | oral | 16mg/kg (16mg/kg) | Journal of Agricultural and Food Chemistry. Vol. 13, Pg. 220, 1965. | |
| rat | LD50 | skin | 113mg/kg (113mg/kg) | Pesticide Manual. Vol. 1, Pg. 263, 1968. | |
| rat | LD50 | unreported | 41mg/kg (41mg/kg) | "Chemistry of Pesticides," Melnikov, N.N., New York, Springer-Verlag New York, Inc., 1971Vol. -, Pg. 193, 1971. |
m-Cumenol methylcarbamate Consensus Reports
EPA Extremely Hazardous Substances List.
m-Cumenol methylcarbamate Safety Profile
Poison by ingestion, skin contact, intraperitoneal, intravenous, intramuscular, and possibly other routes. A pesticide. See also CARBAMATES. When heated to decomposition it emits toxic fumes of NOx.
RIDADR: 2757
HazardClass: 6.1(a)
PackingGroup: I
m-Cumenol methylcarbamate Specification
1.Treatment of m-Cumenol methylcarbamate (64-00-6) in Wastewater,see as follows :
Total removal:3.53 percent
Total biodegradation:0.11 percent
Total sludge adsorption:3.42 percent
Total to air:0.00 percent
(using 10000 hr Bio P,A,S)
2.Reactivity Profile
m-Cumenol methylcarbamate (64-00-6) is a carbamate ester. Carbamates are chemically similar to, but more reactive than amides. Like amides they form polymers such as polyurethane resins. Carbamates are incompatible with strong acids and bases, and especially incompatible with strong reducing agents such as hydrides. Flammable gaseous hydrogen is produced by the combination of active metals or nitrides with carbamates. Strongly oxidizing acids, peroxides, and hydroperoxides are incompatible with carbamates.
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