1-diethylamino-2,4-dinitronaphthalene
ethylamine
A
N-ethyl-2,4-dinitro-1-naphthylamine
B
diethylamine
Conditions | Yield |
---|---|
In water at 30℃; for 1h; | A 100% B n/a |
(N,N-diethylamino)tributyltin
2,5-diethynylthiophene
A
2,5-bis[(tributylstannyl)ethynyl]thiophene
B
diethylamine
Conditions | Yield |
---|---|
In neat (no solvent) stoich. amts., stirring (overnight, room temp., dry atmosphere), evapn. (vac.); | A 99% B n/a |
phenylphosphonic acid bis(N,N-diethylamide)
4-methoxy-aniline
A
phenyl N,N'-bis(p-methoxyphenyl)phosphorodiamidite
B
diethylamine
Conditions | Yield |
---|---|
for 12h; Heating; | A 26.3% B 98.5% |
Conditions | Yield |
---|---|
With aluminum (III) chloride; zinc borohydride In methanol at 60℃; for 10h; Reagent/catalyst; Temperature; Solvent; | A 95.7% B 98.1% |
trimethylsilyl diethylcarbamate
trimethylsilyl <2-(trimethylsiloxy)ethyl>carbamate
A
N,N'-bis-<β-(trimethylsiloxy)>ethylcarbodiimide
B
diethylamine
Conditions | Yield |
---|---|
A 66% B 98% |
4-methoxy-aniline
bis(diethylamino)phenylphosphine
A
N,N'-bis(p-methoxyphenyl)-P-phenylphosphonous diamide
B
diethylamine
Conditions | Yield |
---|---|
for 14h; Heating; | A 83.7% B 98% |
for 14h; Heating; | A 83.7% B 98% |
1-diethylamino-2,4-dinitronaphthalene
methylamine
A
1-(Methylamino)-2,4-dinitronaphthalene
B
diethylamine
Conditions | Yield |
---|---|
In water at 30℃; for 1h; | A 97% B n/a |
bis-(4-hydroxyphenyl)methane
bis(diethylamino)phenylphosphine
B
diethylamine
Conditions | Yield |
---|---|
In neat (no solvent) at 115 - 120℃; for 2h; | A 97% B n/a |
BPA
bis(diethylamino)phenylphosphine
A
4,4′-(propane-2,2-diyl)di(benzene-4,1-diyl) bis(N,N-diethyl-P-phenylphosphonamidite)
B
diethylamine
Conditions | Yield |
---|---|
In neat (no solvent) at 115 - 120℃; for 2h; | A 97% B n/a |
3-(trimethylsilyl)-1-(trimethylstannyl)propyne
Diethylamino-trimethyl-stannan
A
3-(trimethylsilyl)-1,3-bis(trimethylstannyl)propyne
B
3-(trimethylsilyl)-1,1-bis(trimethylstannyl)propadiene
C
(Trimethylsilyl)tris(trimethylstannyl)propadiene
D
diethylamine
Conditions | Yield |
---|---|
In neat (no solvent) heating (180-200°C, 1 h), continuous removal of HNEt2; distn.; elem. anal.; mixt. of propadiene/propyne bis(trimethylastannyl)-derivatives (90:10 %) not separated; | A n/a B n/a C n/a D 96% |
diethylammonium diethylcarbamate
diethylamine
Conditions | Yield |
---|---|
In methanol at 60 - 65℃; for 2h; | 95% |
phenylphosphonic acid bis(N,N-diethylamide)
aniline
A
triphenyl phosphite
B
N,N',N''-triphenylphosphorous triamide
C
phenyl N,N'-diphenylphosphorodiamidite
D
diphenyl phenylphosphoramidite
E
diethylamine
Conditions | Yield |
---|---|
for 17h; Product distribution; Heating; | A n/a B n/a C n/a D n/a E 94.5% |
4-[(diethylamino)methyl]-2,6-bis(1,1-dimethylethyl)phenol
phosphonic acid diethyl ester
A
diethyl 4-hydroxy-3,5-di-tert-butylbenzylphosphonate
B
diethylamine
Conditions | Yield |
---|---|
In toluene for 25h; Heating; | A 94% B n/a |
bis(diethylamino)phenylphosphine
4-bromo-aniline
A
N,N'-bis(p-bromophenyl)-P-phenylphosphonous diamide
B
diethylamine
Conditions | Yield |
---|---|
for 18.5h; Heating; | A 68.1% B 93.6% |
1,3-benzothiazol-2-ylhydrazine
bis(diethylamino)phenylphosphine
A
2-Hydrazono-3-(diethylaminophenylphosphino)-2,3-dihydro-1,3-benzothiazole
B
diethylamine
Conditions | Yield |
---|---|
at 110 - 115℃; under 5 - 10 Torr; for 1h; | A 92.3% B n/a |
bis(diethylamino)phenylphosphine
aniline
A
N,N'-triphenylphosphonous diamide
B
diethylamine
Conditions | Yield |
---|---|
for 20h; Heating; | A 72.2% B 92.1% |
bis(diethylamino)phenylphosphine
2-Chloroaniline
A
N,N'-bis(o-chlorophenyl)-P-phenylphosphonous diamide
B
diethylamine
Conditions | Yield |
---|---|
for 36h; Heating; | A 62.4% B 91.6% |
phenylphosphonic acid bis(N,N-diethylamide)
4-bromo-aniline
A
triphenyl phosphite
B
diethylamine
Conditions | Yield |
---|---|
for 22h; Product distribution; Heating; | A n/a B 91.4% C n/a D n/a E n/a |
Conditions | Yield |
---|---|
With hexaethylphosphoric triamide at 190℃; further reagent; | A 26.8% B 91.3% |
Conditions | Yield |
---|---|
With 4-Hydroxy-4-methyl-2-pentanone at 190℃; | A 26.8% B 91.3% |
O,O'-diethyl thiophosphonate
4-[(diethylamino)methyl]-2,6-bis(1,1-dimethylethyl)phenol
A
diethylamine
Conditions | Yield |
---|---|
In toluene for 25h; Heating; | A n/a B 90% |
ethylene glycol
A
1-thiopropane
B
1,4,6,9-tetraoxa-5λ5-phosphaspiro[4,4]nonane
C
diethylamine
Conditions | Yield |
---|---|
at 120 - 130℃; for 1h; | A n/a B 90% C n/a |
at 120 - 130℃; for 1h; Product distribution; | A n/a B 90% C n/a |
1-Bicyclo[2.2.1]hept-5-en-2-yl-butane-1,2-dione
N,N-diethyl-1,1,1-trimethylsilanamine
A
(Z)-1-Bicyclo[2.2.1]hept-5-en-2-yl-2-trimethylsilanyloxy-but-2-en-1-one
B
diethylamine
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid at 30 - 40℃; for 18h; | A 90% B n/a |
1-(3-Methyl-bicyclo[2.2.1]hept-5-en-2-yl)-butane-1,2-dione
N,N-diethyl-1,1,1-trimethylsilanamine
A
(Z)-1-(3-Methyl-bicyclo[2.2.1]hept-5-en-2-yl)-2-trimethylsilanyloxy-but-2-en-1-one
B
diethylamine
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid at 30 - 40℃; for 18h; | A 90% B n/a |
carbon monoxide
benzenenesulfenyl dimethylamine
A
N,N'-diethylurea
B
N,N,N',N'-tetraethyloxamide
C
diethylamine
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine) palladium(0) In pyridine at 80℃; under 14701.2 Torr; for 10h; Carbonylation; | A n/a B 1.4 % Spectr. C 3 % Spectr. D 90% |
2-hydrazino-6-methylbenzothiazole
bis(diethylamino)phenylphosphine
A
C18H23N4PS
B
diethylamine
Conditions | Yield |
---|---|
at 110 - 115℃; under 5 - 10 Torr; for 1h; | A 89.7% B n/a |
Conditions | Yield |
---|---|
With carbon monoxide; hexarhodium hexadecacarbonyl In 2-ethoxy-ethanol; water at 40℃; under 12160 Torr; for 5h; | 89% |
With N,N,N'N'-tetramethyl-1,3-propanediamine; carbon monoxide; water; hexarhodium hexadecacarbonyl In 2-ethoxy-ethanol at 40℃; under 6080 Torr; for 5h; | 93 % Chromat. |
With N,N,N'N'-tetramethyl-1,3-propanediamine; carbon monoxide; water; hexarhodium hexadecacarbonyl In 2-ethoxy-ethanol at 40℃; under 6080 Torr; for 5h; Product distribution; Mechanism; (CH3)2NC3H6NH-substituted polystyrene instead of TMPDA; analogous reaction of other hydroxylamines; | 93 % Chromat. |
(2-hydroxyethyl)urea
N,N-diethyl-1,1,1-trimethylsilanamine
A
diethylamine
B
N-<2-(trimethylsiloxy)ethyl>-N'-(trimethylsilyl)urea
Conditions | Yield |
---|---|
With ammonium sulfate at 120℃; for 1h; | A 82% B 89% |
bis(diethylamino)phenylphosphine
(4-chloro-1,3-benzothiazol-2-yl)hydrazine
A
C17H20ClN4PS
B
diethylamine
Conditions | Yield |
---|---|
at 110 - 115℃; under 5 - 10 Torr; for 1h; | A 88.5% B n/a |
1-butanethiol
dibutyl diethylphosphoramidodithioite
A
merphos
B
diethylamine
Conditions | Yield |
---|---|
for 0.5h; Ambient temperature; | A 88% B 77% |
1,3-propanesultone
diethylamine
3-(diethylamino)propane-1-sulfonic acid
Conditions | Yield |
---|---|
In dichloromethane at 10℃; for 1h; Product distribution / selectivity; | 100% |
In dichloromethane Inert atmosphere; | 53% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 6h; | 100% |
With sodium carbonate In tert-butyl methyl ether; water at 15 - 25℃; for 1h; Schotten-Baumann Reaction; Inert atmosphere; | 98.7% |
In toluene at 50℃; | 90% |
Conditions | Yield |
---|---|
With copper diacetate In water at 20℃; for 12h; aza-Michael addition; | 100% |
copper diacetate In water at 20℃; for 15h; aza-type Michael addition; | 100% |
at 0℃; Inert atmosphere; | 99% |
2-bromobenzoic acid chloride
diethylamine
2-bromo-N,N-diethylbenzamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 0.5h; Inert atmosphere; | 100% |
In dichloromethane at 0 - 20℃; Schlenk technique; | 99% |
In dichloromethane at 0 - 20℃; for 0.5h; | 95% |
formaldehyd
4-acetaminophenol
diethylamine
N-{3-[(diethylamino)methyl]-4-hydroxyphenyl}acetamide
Conditions | Yield |
---|---|
In ethanol at 80℃; for 1.5h; Microwave irradiation; | 100% |
In ethanol for 12h; Heating; | 80% |
In ethanol at 80℃; for 1h; Microwave irradiation; | 77% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 14h; Inert atmosphere; | 100% |
With triethylamine In dichloromethane at 0 - 20℃; for 14h; Inert atmosphere; | 100% |
With diethyl ether; triethylamine | |
With benzene |
fumaryl dichloride
diethylamine
N1,N1,N4,N4-tetraethylfumaramide
Conditions | Yield |
---|---|
In diethyl ether at 0 - 20℃; Inert atmosphere; | 100% |
With diethyl ether |
Conditions | Yield |
---|---|
With copper diacetate In water at 20℃; for 12h; aza-Michael addition; | 100% |
iron(III) chloride In water at 20℃; for 15h; aza-type Michael addition; | 100% |
1-butyl-3-methylimidazolium Tetrafluoroborate In water at 20℃; for 7h; aza-Michael reaction; | 97% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; | 100% |
With benzene | |
With diethyl ether | |
In benzene | |
With sodium carbonate In benzene at 0 - 5℃; |
Conditions | Yield |
---|---|
In dichloromethane; water at 5℃; Temperature; Solvent; | 100% |
With triethylamine In dichloromethane at 0℃; | 99% |
With triethylamine In 1,2-dichloro-ethane at 10 - 20℃; for 3h; Cooling with ice; | 95% |
formaldehyd
diethylamine
phenylacetylene
diethyl-(3-phenyl-prop-2-ynyl)-amine
Conditions | Yield |
---|---|
With copper dichloride at 80℃; under 150.015 Torr; for 3h; Mannich reaction; | 100% |
With silver nitrate at 105℃; for 0.133333h; microwave irradiation; | 99% |
copper(l) iodide In water; dimethyl sulfoxide at 30℃; for 10h; | 98% |
Conditions | Yield |
---|---|
In ethanol; water at 60℃; for 6h; | 100% |
In acetonitrile at 25℃; for 2h; Solvent; | 85% |
With ethanol | |
With sodium carbonate In acetone for 5h; Substitution; Heating; | |
In acetonitrile at 25℃; Kinetics; Solvent; |
diethylamine
hydrocinnamic acid chloride
N,N-diethyl-3-phenylpropanamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 14h; Inert atmosphere; | 100% |
With triethylamine In dichloromethane at 0 - 20℃; for 14h; Inert atmosphere; | 96% |
Conditions | Yield |
---|---|
With copper diacetate In water at 20℃; for 12h; aza-Michael addition; | 100% |
iron(III) chloride In dichloromethane at 25℃; for 42h; Product distribution; various catalysts and further amines with various Michael acceptors; | 96% |
iron(III) chloride In dichloromethane at 25℃; for 42h; | 96% |
Conditions | Yield |
---|---|
With phosphorus trichloride In diethyl ether at -78 - 20℃; for 2h; | 100% |
With phosphorus trichloride In diethyl ether at -78 - 20℃; Inert atmosphere; | 100% |
With phosphorus trichloride In diethyl ether at -78 - 20℃; for 2h; | 100% |
Conditions | Yield |
---|---|
With [NO(1+)*18-crown-6*H(NO3)2(1-)] In dichloromethane at 20℃; for 0.0833333h; | 100% |
With magnesium hydrogen sulfate; silica gel; sodium nitrite In dichloromethane at 20℃; for 1h; Nitrosation; | 98% |
With aluminium trichloride; silica gel; sodium nitrite In dichloromethane at 20℃; for 0.5h; Nitrosation; | 98% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 0℃; Inert atmosphere; | 100% |
In tetrahydrofuran at 0℃; for 0.0833333h; Inert atmosphere; | 100% |
With triethylamine In methanol; toluene at 0℃; for 2h; | 95% |
diethylamine
dimethyl acetylenedicarboxylate
dimethyl (2E)-2-(diethylamino)but-2-enedioate
Conditions | Yield |
---|---|
In water at 20℃; for 2h; Michael-type addition; | 100% |
In diethyl ether |
Conditions | Yield |
---|---|
In acetonitrile at 30℃; under 6750540 Torr; for 96h; | 100% |
Stage #1: diethylamine With diisobutylaluminium hydride In tetrahydrofuran; toluene Stage #2: 4-butanolide In tetrahydrofuran at 45℃; for 2h; | 72% |
carbon monoxide
benzyl bromide
diethylamine
S-benzyl N,N-diethylthiolcarbamate
Conditions | Yield |
---|---|
With sulfur; selenium In tetrahydrofuran 1.) 30 deg C; 2.) rt.; | 100% |
With n-butyllithium; sulfur 1.) THF/hexane, from -78 deg C to -20 deg C; 2.) - 78 deg C; 3.) 20 deg C, 1 atm, 2 h; Yield given. Multistep reaction; | |
Yield given. Multistep reaction; |
7-chloro-1,3-dimethyl-6-azalumazine
diethylamine
7-(diethylamino)-1,3-dimethyl-6-azalumazine
Conditions | Yield |
---|---|
In dichloromethane for 2.5h; | 100% |
formaldehyd
N-(3-sec-Butyl-4-hydroxy-phenyl)-acetamide
diethylamine
N-(3-sec-Butyl-5-diethylaminomethyl-4-hydroxy-phenyl)-acetamide
Conditions | Yield |
---|---|
In ethanol for 48h; Heating; | 100% |
formaldehyd
N-(6-Hydroxy-2',5'-dimethoxy-biphenyl-3-yl)-acetamide
diethylamine
N-(5-Diethylaminomethyl-6-hydroxy-2',5'-dimethoxy-biphenyl-3-yl)-acetamide
Conditions | Yield |
---|---|
In ethanol; water Heating; | 100% |
formaldehyd
N-(6-Hydroxy-2'-trifluoromethyl-biphenyl-3-yl)-acetamide
diethylamine
N-(5-Diethylaminomethyl-6-hydroxy-2'-trifluoromethyl-biphenyl-3-yl)-acetamide
Conditions | Yield |
---|---|
In ethanol; water Heating; | 100% |
formaldehyd
3a,3b,4,4a,7a,8,8b-octahydro-4,8-ethenopyrrolo<3',4':3,4>cyclobut<1,2-f>isoindole-1,3,5,7<2H,6H>tetrone
diethylamine
C24H34N4O4
Conditions | Yield |
---|---|
In water; N,N-dimethyl-formamide at 70℃; for 6h; | 100% |
ethylene glycol diacrylate
diethylamine
1,10-bis-diethylamino-4,7-dioxa-3,8-dioxodecane
Conditions | Yield |
---|---|
In diethyl ether for 18h; Ambient temperature; | 100% |
Diethylamino-(chlormethyl)-chlorphosphin
diethylamine
P-(Chloromethyl)-N,N,N',N'-tetraethylphosphonous diamide
Conditions | Yield |
---|---|
In diethyl ether | 100% |
o-formylbenzonitrile
diethylamine
3-Diethylamino-2,3-dihydro-isoindol-1-one
Conditions | Yield |
---|---|
at 40℃; for 1h; | 100% |
(E)-4-Ethoxy-1,1,1-trifluoro-3-buten-2-one
diethylamine
β-(N,N-diethylamino)vinyltrifluoromethylketone
Conditions | Yield |
---|---|
In acetonitrile Ambient temperature; | 100% |
In cyclohexane at 19.9℃; Rate constant; other solvents; ΔG(excit.), ΔH(excit.), ΔS(excit.); | |
In cyclohexane at 19.9℃; Yield given; |
4-bromo-4-methyl-1-phenyl-pent-1-yn-3-one
diethylamine
(Z)-4-Bromo-1-diethylamino-4-methyl-1-phenyl-pent-1-en-3-one
Conditions | Yield |
---|---|
In hexane Ambient temperature; | 100% |
The Diethylamine, with the cas register number 109-89-7, has other synonyms, such as (c2h5)2nh; ai3-24215; detn; diaethylamin; diethamine; diethylamin; dietilamina; dwuetyloamina.
The characteristics of this chemical could be summarized as: (1)ACD/LogP: 0.63; (2)ACD/LogD (pH 5.5): -2.46; (3)ACD/LogD (pH 7.4): -2.28; (4)ACD/BCF (pH 5.5): 1; (5)ACD/BCF (pH 7.4): 1; (6)ACD/KOC (pH 5.5): 1; (7)ACD/KOC (pH 7.4): 1; (8)#H bond acceptors: 1; (9)#H bond donors: 1; (10)#Freely Rotating Bonds: 2; (11)Polar Surface Area: 3.24; (12)Index of Refraction: 1.384 ; (13)Molar Refractivity: 24.17 cm3; (14)Molar Volume: 103.3 cm3; (15)Polarizability: 9.58 ×10-24 cm3; (16)Surface Tension: 20.2 dyne/cm; (17)Density: 0.707 g/cm3; (18)Enthalpy of Vaporization: 29.06 kJ/mol; (19)Boiling Point: 57.3 °C at 760 mmHg; (20)Vapour Pressure: 218 mmHg at 25°C.
This is a kind of colorless combustible liquid with strong smell of ammonia, and it is complete soluble in water, ethanol and ethyl ether. And it is sensitive to air and incompatible with strong oxidizing agents, so while keeping, you should keep it under argon in the room temperature.
Being a kind of highly flammable chemical, it may catch fire in contact with air, only needing brief contact with an ignition source, and it has a very low flash point or evolve highly flammable gases in contact with water. Besides, it is corrosive, and it may destroy living tissue on contact. Then it is harmful by inhalation, in contact with skin or if swallowed and it could cause severe burns.
While using this chemical, you should take the following instructions to protece yourself. Keep away from sources of ignition - No smoking and keep in a cool place. Wear suitable protective clothing, gloves and eye/face protection, and if in case of contact with eyes, rinse immediately with plenty of water and seek medical advice; if in case of accident or if you feel unwell seek medical advice immediately (show the label where possible). Lastly, do not empty into drains. You could also refer to WGK Germany 1 to get more safety information.
Diethylamine could be applied in many ways, such as being the analytical reagent and preservative and also be used in making organic synthesis and dyeing. Besides, it could also be as the intermediates, such as for pesticide, such as phosphamidon and pyrimithate, and for herbicide, such as benthiocarb and napropamide. What's more, it could be the solvent and chemical material intermediate to make the medicine, such as procaine, chloroquine, nikethamide, Coraminum and sulfanilamide, and other different fields, such as thiofide, beneficiation reagent, textile assistant, fungicide, corrosion inhibitor, polymerization inhibitor, antifreeze agent and so on.
As to its product categories, there are various, including pharmaceutical intermediates; intermediates of dyes and pigments; chemical synthesis; organic bases; synthetic reagents; essential chemicals; reagent plus; routine reagents; analytical reagents for general use; c-d, puriss p.a.; puriss p.a. And its preparation products are numerous, containing 4-phenyl-1-(p-tolylsulphonyl)piperidine-4-carboxylic acid , montelukast, 4'-iodoacetophenone, 4,6-dimethyl-1h-pyrazolo[3,4-b]pyridin-3-amine, 2-amino-6-methyl-4,5,6,7-tetrahydro-1-benzothiophene-3-carbonitrile, 2-amino-5,6-dihydro-4h-cyclopenta[b]thiophene-3-carbonitrile, 1,4,6-trimethyl-1h-pyrazolo[3,4-b]pyridin-3-ylamine ,97%, 7-(diethylamino)-5-methyl-s-triazolo[1,5-a]pyrimidine, diethylcarbamyl chloride, benzyl cinnamate, 2-amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carbonitrile, 2-amino-4,5-dimethyl-thiophene-3-carbonitrile, 3-(diethylamino)propanoic acid, benzyl salicylate, 5-amino-3-methyl-thiophene-2,4-dicarboxylic acid dimethyl ester, (5-bromo-pyrimidin-2-yl)-diethyl-amine, while its raw material are the etanol, ammonia, hydrogen, 2-ethylaniline, and 2-(ethylamino)ethanol.
Additionally, you could convert the following data information into the molecular structure:
SMILES:N(CC)CC
InChI:InChI=1/C4H11N/c1-3-5-4-2/h5H,3-4H2,1-2H3
InChIKey:HPNMFZURTQLUMO-UHFFFAOYAD
Below are the toxicity information of this chemical:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mammal (species unspecified) | LC50 | inhalation | 5000mg/m3 (5000mg/m3) | Toksikologiya Novykh Promyshlennykh Khimicheskikh Veshchestv. Toxicology of New Industrial Chemical Substances. For English translation, see TNICS*. Vol. 14, Pg. 80, 1975. | |
mouse | LCLo | inhalation | 3gm/m3/2H (3000mg/m3) | BRAIN AND COVERINGS: RECORDINGS FROM SPECIFIC AREAS OF CNS LUNGS, THORAX, OR RESPIRATION: ACUTE PULMONARY EDEMA LIVER: FATTY LIVER DEGERATION | Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 20(4), Pg. 28, 1955. |
mouse | LD50 | intraperitoneal | 585mg/kg (585mg/kg) | Yakugaku Zasshi. Journal of Pharmacy. Vol. 97, Pg. 1117, 1977. | |
mouse | LD50 | oral | 500mg/kg (500mg/kg) | BEHAVIORAL: SLEEP BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) | Biomedica Biochimica Acta. Vol. 44, Pg. 795, 1985. |
rabbit | LCLo | inhalation | 20gm/m3 (20000mg/m3) | SENSE ORGANS AND SPECIAL SENSES: OTHER CHANGES: OLFACTION LUNGS, THORAX, OR RESPIRATION: EMPHYSEMA LIVER: FATTY LIVER DEGERATION | "Voprosy Promyshlennoi Toksikologii," Pravdin, N.S., ed., Akademiya Meditsinskikh Nauk-SSSR, Moscos, Russia, 1960Vol. -, Pg. 176, 1960. |
rabbit | LD50 | skin | 820uL/kg (0.82mL/kg) | AMA Archives of Industrial Hygiene and Occupational Medicine. Vol. 4, Pg. 119, 1951. | |
rat | LC50 | inhalation | 4000ppm/4H (4000ppm) | Archives of Environmental Health. Vol. 1, Pg. 343, 1960. | |
rat | LD50 | oral | 540mg/kg (540mg/kg) | Archives of Environmental Health. Vol. 1, Pg. 343, 1960. | |
rat | LDLo | intraperitoneal | 50mg/kg (50mg/kg) | Farmakologiya i Toksikologiya Vol. 31, Pg. 238, 1968. |
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