Product Name

  • Name

    1,3-Propanediamine,N1-(3-aminopropyl)-N1-methyl-

  • EINECS 203-336-8
  • CAS No. 105-83-9
  • Article Data7
  • CAS DataBase
  • Density 0.915 g/cm3
  • Solubility 1000g/L at 20℃
  • Melting Point -30--28 °C
  • Formula C7H19N3
  • Boiling Point 252.9 °C at 760 mmHg
  • Molecular Weight 145.248
  • Flash Point 102.8 °C
  • Transport Information UN 2810 6.1/PG 2
  • Appearance
  • Safety 26-36/37/39-45
  • Risk Codes 22-23/24-34
  • Molecular Structure Molecular Structure of 105-83-9 (1,3-Propanediamine,N1-(3-aminopropyl)-N1-methyl-)
  • Hazard Symbols ToxicT
  • Synonyms Dipropylamine, 3,3'-diamino-N-methyl-(6CI,7CI,8CI);(7-Amino-4-methyl-4-azaheptyl)amine;1,7-Diamino-4-methyl-4-azaheptane;3,3'-Diamino-N-methyldipropylamine;4-Aza-4-methylheptane-1,7-diamine;5-Methyl-1,5,9-triazanonane;5-Methyldipropylenetriamine;Bis(3-aminopropyl)methylamine;Bis(w-aminopropyl)methylamine;Di(g-aminopropyl)methylamine;Methylbis(3-aminopropyl)amine;Methyliminobispropylamine;N,N'-Bis(3-aminopropyl)methylamine;N-(3-Aminopropyl)-N-methyl-1,3-propanediamine;N-Methyl-N,N-bis(3-aminopropyl)amine;N'-Methyl-3,3'-diaminodipropylamine;
  • PSA 55.28000
  • LogP 1.01640

Synthetic route

Bis(2-cyanoethyl)methylamine
1555-58-4

Bis(2-cyanoethyl)methylamine

3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

Conditions
ConditionsYield
With hydrogen; sodium hydroxide In ethanol at 90℃; under 15001.5 Torr; Autoclave; Green chemistry;85%
With sodium; butan-1-ol
With ammonia; nickel at 100℃; under 73550.8 Torr; Hydrogenation;
Bis(2-cyanoethyl)methylamine
1555-58-4

Bis(2-cyanoethyl)methylamine

A

1-methyl-[1,5]diazocane
4318-36-9

1-methyl-[1,5]diazocane

B

3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

Conditions
ConditionsYield
With ammonia; nickel at 90 - 100℃; under 73550.8 Torr; Hydrogenation;
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

1-methyl-4-nitro-2-trichloroacetylpyrrole
120122-47-6

1-methyl-4-nitro-2-trichloroacetylpyrrole

1-methyl-N-[3-[methyl-[3-[(1-methyl-4-nitro-pyrrole-2-carbonyl)amino]propyl]amino]propyl]-4-nitro-pyrrole-2-carboxamide
158551-29-2

1-methyl-N-[3-[methyl-[3-[(1-methyl-4-nitro-pyrrole-2-carbonyl)amino]propyl]amino]propyl]-4-nitro-pyrrole-2-carboxamide

Conditions
ConditionsYield
In tetrahydrofuran at 20℃;100%
N-(Benzyloxycarbonyloxy)succinimide
13139-17-8

N-(Benzyloxycarbonyloxy)succinimide

3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

C23H31N3O4
1307864-23-8

C23H31N3O4

Conditions
ConditionsYield
In chloroform at 20℃; for 16h;100%
In chloroform at 20℃; for 16h;
In chloroform at 20℃; for 16h;
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

phenyl isothiocyanate
103-72-0

phenyl isothiocyanate

C21H29N5S2
1229624-20-7

C21H29N5S2

Conditions
ConditionsYield
In tetrahydrofuran at 20℃;100%
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

2-chloro-3-methyl-4-quinolinecarboxylic acid chloride
431078-96-5

2-chloro-3-methyl-4-quinolinecarboxylic acid chloride

C29H31Cl2N5O2
1620066-15-0

C29H31Cl2N5O2

Conditions
ConditionsYield
With triethylamine In chloroform at 20℃; for 48h;98%
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

3-(8-methoxypyrrolo[1,2-a]quinoxalin-4-yl)benzaldehyde

3-(8-methoxypyrrolo[1,2-a]quinoxalin-4-yl)benzaldehyde

bis{N-[3-(8-methoxypyrrolo[1,2-a]quinoxalin-4-yl)benzylidene]-3-aminopropyl}methylamine

bis{N-[3-(8-methoxypyrrolo[1,2-a]quinoxalin-4-yl)benzylidene]-3-aminopropyl}methylamine

Conditions
ConditionsYield
In ethanol for 5h; Reflux;98%
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

2-(4-formylphenyl)-1,10-phenanthroline

2-(4-formylphenyl)-1,10-phenanthroline

bis{N-[4-(1,10-phenanthrolin-2-yl)benzylidene]-3-aminopropyl}methylamine

bis{N-[4-(1,10-phenanthrolin-2-yl)benzylidene]-3-aminopropyl}methylamine

Conditions
ConditionsYield
In ethanol for 5h; Reflux;98%
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

(1,1-dimethyl-2-phenylethyl) hydrogen benzene-1,2-dicarboxylate
170233-80-4

(1,1-dimethyl-2-phenylethyl) hydrogen benzene-1,2-dicarboxylate

C43H51N3O6

C43H51N3O6

Conditions
ConditionsYield
With TEA; chloroformic acid ethyl ester In dichloromethane97%
copper(II) perchlorate hexahydrate

copper(II) perchlorate hexahydrate

3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

sodium nitrite
7632-00-0

sodium nitrite

[Cu(3,3'-diamino-N-methyldipropylamine)(ONO)(H2O)]ClO4
890850-35-8

[Cu(3,3'-diamino-N-methyldipropylamine)(ONO)(H2O)]ClO4

Conditions
ConditionsYield
In methanol soln. of Cu salt added to soln. of org. compd., hot soln. of NaNO2 addeddropwise, heated for 10 min; hot filtered, allowed to crystallize at room temp., filtered, washed with ether, air-dried; elem. anal.;97%
...Expand
ethanol
64-17-5

ethanol

3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

1,2-bis(4-tert-butyl-2,6-diformylphenylsulfanyl)ethane
255367-21-6

1,2-bis(4-tert-butyl-2,6-diformylphenylsulfanyl)ethane

C40H68N6S2*0.5C2H6O

C40H68N6S2*0.5C2H6O

Conditions
ConditionsYield
Stage #1: ethanol; 3,3'-Diamino-N-methyldipropylamine; 1,2-bis(4-tert-butyl-2,6-diformylphenylsulfanyl)ethane In dichloromethane at 0 - 20℃; for 18h;
Stage #2: With sodium tetrahydroborate at 20℃; for 4h;		97%
...Expand
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

4-(3-ethoxypyrrolo[1,2-a]quinoxalin-4-yl)benzaldehyde

4-(3-ethoxypyrrolo[1,2-a]quinoxalin-4-yl)benzaldehyde

bis{N-[4-(3-ethoxypyrrolo[1,2-a]quinoxalin-4-yl)benzylidene]-3-aminopropyl}methylamine

bis{N-[4-(3-ethoxypyrrolo[1,2-a]quinoxalin-4-yl)benzylidene]-3-aminopropyl}methylamine

Conditions
ConditionsYield
In ethanol for 5h; Reflux;97%
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

3-(pyrrolo[1,2-a]quinoxalin-4-yl)benzaldehyde

3-(pyrrolo[1,2-a]quinoxalin-4-yl)benzaldehyde

bis{N-[3-(pyrrolo[1,2-a]quinoxalin-4-yl)benzylidene]-3-aminopropyl}methylamine

bis{N-[3-(pyrrolo[1,2-a]quinoxalin-4-yl)benzylidene]-3-aminopropyl}methylamine

Conditions
ConditionsYield
In ethanol for 5h; Reflux;97%
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

di-tert-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

N-(3-aminopropyl)-N-(3-tert-butyloxycarbonyl-aminopropyl)-N-methylamine
87530-14-1

N-(3-aminopropyl)-N-(3-tert-butyloxycarbonyl-aminopropyl)-N-methylamine

Conditions
ConditionsYield
In tetrahydrofuran96%
In tetrahydrofuran96%
In tetrahydrofuran83%
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

(E,E)-5-(3,4,5-trimethoxyphenyl)-2,4-pentadienoic acid
28010-23-3

(E,E)-5-(3,4,5-trimethoxyphenyl)-2,4-pentadienoic acid

N,N-bis[N-[5-(3,4,5-trimethoxyphenyl)penta-(2E,4E)-dienoyl]-3-aminopropyl]methylamine

N,N-bis[N-[5-(3,4,5-trimethoxyphenyl)penta-(2E,4E)-dienoyl]-3-aminopropyl]methylamine

Conditions
ConditionsYield
96%
ammonium thiocyanate

ammonium thiocyanate

copper(II) perchlorate hexahydrate

copper(II) perchlorate hexahydrate

3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

[Cu2(3,3'-diamino-N-methyldipropylamine)2(μN,S-NCS)2](ClO4)2

[Cu2(3,3'-diamino-N-methyldipropylamine)2(μN,S-NCS)2](ClO4)2

Conditions
ConditionsYield
In methanol soln. of NH4CNS added dropwise to mixt. of soln. of Cu salt and of org. compd., heated for 5 min; hot filtered, allowed to crystallize at room temp., filtered, washed with ether, air-dried; elem. anal.;96%
...Expand
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

4-(9-methoxypyrrolo[1,2-a]quinoxalin-4-yl)benzaldehyde

4-(9-methoxypyrrolo[1,2-a]quinoxalin-4-yl)benzaldehyde

bis{N-[4-(9-methoxypyrrolo[1,2-a]quinoxalin-4-yl)benzylidene]-3-aminopropyl}methylamine

bis{N-[4-(9-methoxypyrrolo[1,2-a]quinoxalin-4-yl)benzylidene]-3-aminopropyl}methylamine

Conditions
ConditionsYield
In ethanol for 5h; Reflux;96%
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

C19H14N2O2

C19H14N2O2

bis{N-[4-(7-methoxypyrrolo[1,2-a]quinoxalin-4-yl)benzylidene]-3-aminopropyl}methylamine

bis{N-[4-(7-methoxypyrrolo[1,2-a]quinoxalin-4-yl)benzylidene]-3-aminopropyl}methylamine

Conditions
ConditionsYield
In ethanol for 5h; Reflux;96%
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

C19H14N2O2

C19H14N2O2

bis{N-[4-(8-methoxypyrrolo[1,2-a]quinoxalin-4-yl)benzylidene]-3-aminopropyl}methylamine

bis{N-[4-(8-methoxypyrrolo[1,2-a]quinoxalin-4-yl)benzylidene]-3-aminopropyl}methylamine

Conditions
ConditionsYield
In ethanol for 5h; Reflux;96%
(E)-3-(5,6-dimethoxy-1,1-dimethyl-2-indenyl)-2-propenoic acid
203722-25-2

(E)-3-(5,6-dimethoxy-1,1-dimethyl-2-indenyl)-2-propenoic acid

3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

N,N-bis[N-[3-(5,6-dimethoxy-1,1-dimethyl-2-indenyl)prop-(2E)-enoyl]-3-aminopropyl]methylamine

N,N-bis[N-[3-(5,6-dimethoxy-1,1-dimethyl-2-indenyl)prop-(2E)-enoyl]-3-aminopropyl]methylamine

Conditions
ConditionsYield
95%
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

Co(OCHOC6H2Cl2)2
49860-79-9

Co(OCHOC6H2Cl2)2

Co((CH2)3NCHC6H2Cl2O)2NCH3
38625-76-2

Co((CH2)3NCHC6H2Cl2O)2NCH3

Conditions
ConditionsYield
In methanol under N2 soln. was refluxed for 30 min; soln. was concd. in vac., allowed to stand at room temp., prisms were collected by suction, washed with methanol, dried in vac. dessicator; elem. anal.;95%
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

molybdenum hexacarbonyl
13939-06-5, 199620-15-0

molybdenum hexacarbonyl

fac-[(H2N(CH2)3NMe(CH2)3NH2)Mo(CO)3]
161334-73-2

fac-[(H2N(CH2)3NMe(CH2)3NH2)Mo(CO)3]

Conditions
ConditionsYield
In dibutyl ether N2-atmosphere; slight excess metal carbonyl, refluxing for 2 h (returning sublimed hexacarbonyl into reaction vessel); cooling to room temp., collection of ppt., washing (hexane), drying (vac., 50°C);95%
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

C17H13ClNO2(1+)*I(1-)

C17H13ClNO2(1+)*I(1-)

11-((3-((3-aminopropyl)(methyl)amino)propyl)amino)-7-methoxy-5-methylbenzofuro[3,2-b]quinolin-5-ium iodide
1587729-29-0

11-((3-((3-aminopropyl)(methyl)amino)propyl)amino)-7-methoxy-5-methylbenzofuro[3,2-b]quinolin-5-ium iodide

Conditions
ConditionsYield
at 120℃; for 0.5h;95%
In 2-methoxy-ethanol at 120℃; for 0.5h;1.36 g
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

3,5-di-tert-butyl-2-hydroxybenzaldehyde
37942-07-7

3,5-di-tert-butyl-2-hydroxybenzaldehyde

N,N′-bis(3,5-di-tert-butyl-2-hydroxybenzyliden)-1,7-diamino-4-methyl-4-azaheptane

N,N′-bis(3,5-di-tert-butyl-2-hydroxybenzyliden)-1,7-diamino-4-methyl-4-azaheptane

Conditions
ConditionsYield
In methanol at 20℃; for 2h; Inert atmosphere; Schlenk technique;94%
In ethanol for 1h; Heating;
In ethanol Reflux;
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

3,4-diethoxy-3-cyclobuten-1,2-dione
5231-87-8

3,4-diethoxy-3-cyclobuten-1,2-dione

3,3'-[N,N'-[(methylimino)di-3,1-propanediyldiimino]]bis(4-ethoxy-3-cyclobutene-1,2-dione)
679427-49-7

3,3'-[N,N'-[(methylimino)di-3,1-propanediyldiimino]]bis(4-ethoxy-3-cyclobutene-1,2-dione)

Conditions
ConditionsYield
In diethyl ether at 20℃; for 12h;94%
In diethyl ether at 20℃;74%
In diethyl ether
In diethyl ether at 20℃;
In diethyl ether at 20℃; for 12h; Inert atmosphere;
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

C33H35N3O6

C33H35N3O6

Conditions
ConditionsYield
In ethanol94%
1-chloro-7-methoxy-4-nitro-10H-acridin-9-one
21814-48-2

1-chloro-7-methoxy-4-nitro-10H-acridin-9-one

3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

1,1'-<(methylimino)bis(3,1-propanediylimino)>bis<7-methoxy-4-nitro-9(10H)-acridinone>

1,1'-<(methylimino)bis(3,1-propanediylimino)>bis<7-methoxy-4-nitro-9(10H)-acridinone>

Conditions
ConditionsYield
With triethylamine In dimethyl sulfoxide at 80℃; for 3h;93%
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

3,6-dichloro-O-anisic acid
1918-00-9

3,6-dichloro-O-anisic acid

C7H19N3*2C8H6Cl2O3

C7H19N3*2C8H6Cl2O3

Conditions
ConditionsYield
In methanol at 25℃; under 759.826 Torr;92%
3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

mitomycin A
4055-39-4

mitomycin A

C37H49N9O10

C37H49N9O10

Conditions
ConditionsYield
In methanol; N,N-dimethyl-formamide at 20℃; for 4h;91%
sodium azide

sodium azide

copper(II) perchlorate hexahydrate

copper(II) perchlorate hexahydrate

3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

[Cu2(μ1,3-N3)2(methyldipropylenetriamine)2](ClO4)2

[Cu2(μ1,3-N3)2(methyldipropylenetriamine)2](ClO4)2

Conditions
ConditionsYield
In methanol hot suspn. of NaN3 in methanol added dropwise to soln. of Cu salt and triamine in methanol; soln. quickly filtered, filtrate heated in steam bath for 5 min, soln. kept at room temp. for 1 h; crystals filtered off; washed with ether; air dried; elem. anal.;91%
In water aq. soln. of NaN3 added dropwise to soln. of Cu salt and triamine in H2O; stirred for 10 min, left to crystallize at room temp.; crystals filtered off; washed with EtOH and ether; air dried; further crop of crystals from mother liquor which was kept at room temp. for 4 d;86%
...Expand
2,6-Bis(2-formylphenoxymethyl)pyridine
66433-95-2

2,6-Bis(2-formylphenoxymethyl)pyridine

holmium(III) nitrate hydrate

holmium(III) nitrate hydrate

3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

[Ho(15-methyl-3.27-dioxa-11.15.19.33-tetraazatetracyclo[27.3.1.O(4.9).O(21,26)]tritiaconta-1(32).4(9).5.7.10.19.21(26).22.24.29(33).30-nonaene)][NO3]3*4H2O

[Ho(15-methyl-3.27-dioxa-11.15.19.33-tetraazatetracyclo[27.3.1.O(4.9).O(21,26)]tritiaconta-1(32).4(9).5.7.10.19.21(26).22.24.29(33).30-nonaene)][NO3]3*4H2O

Conditions
ConditionsYield
In not given 2,6-bis(2-formylphenoxymethyl)pyridine and Ho(NO3)3*nH2O were dissolved in hot MeOH or EtOH, soln. N,N-bis(3-aminopropyl)methylamine in MeOH or EtOH was added dropwise and refluxed for 3-4 h; react. mixt. was allowed to cool to room temp. and concd., Et2O was added, ppt. was filtered and dried in vacuo; elem. anal.;91%
...Expand
sodium hexanitrocobaltate(III)

sodium hexanitrocobaltate(III)

3,3'-Diamino-N-methyldipropylamine
105-83-9

3,3'-Diamino-N-methyldipropylamine

[Co(5-methyl-1,5,9-triazanonane)(NO2)3]
312712-70-2

[Co(5-methyl-1,5,9-triazanonane)(NO2)3]

Conditions
ConditionsYield
In water aq. soln. of ligand was added dropwise to hot aq. soln. of Co complex; filtered; heated on steam bath with stirring for 15 min; after 2 h filtered; washed (H2O, MeOH, ether); air-dried; elem. anal.;91%

N,N-Bis(3-aminopropyl)methylamine Consensus Reports

Reported in EPA TSCA Inventory.

N,N-Bis(3-aminopropyl)methylamine Specification

The N,N-Bis(3-aminopropyl)methylamine with CAS registry number of 105-83-9 is also called 1,3-Propanediamine,N1-(3-aminopropyl)-N1-methyl-. Its EINECS registry number is 203-336-8. The IUPAC name is N'-(3-aminopropyl)-N'-methylpropane-1,3-diamine. In addition, the molecular formula is C7H19N3 and the molecular weight is 145.24. It belongs to the classes of Pharmaceutical Raw Materials; Nitrogen Compounds; Organic Building Blocks; Polyamines.

Physical properties about this chemical are: (1)ACD/LogP: -0.65; (2)ACD/LogD (pH 5.5): -5.55; (3)ACD/LogD (pH 7.4): -4.78; (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: 3; (9)#H bond donors: 4; (10)#Freely Rotating Bonds: 8; (11)Polar Surface Area: 9.72 Å2; (12)Index of Refraction: 1.482; (13)Molar Refractivity: 45.27 cm3; (14)Molar Volume: 158.6 cm3; (15)Polarizability: 17.94 ×10-24cm3; (16)Surface Tension: 38.1 dyne/cm; (17)Density: 0.915 g/cm3; (18)Flash Point: 102.8 °C; (19)Enthalpy of Vaporization: 49.03 kJ/mol; (20)Boiling Point: 252.9 °C at 760 mmHg; (21)Vapour Pressure: 0.0188 mmHg at 25°C.

Uses of N,N-Bis(3-aminopropyl)methylamine: it can react with 3-Anilinomethylen-2,4-chromandion to get N,N'-Bis-[(2,4-dioxochroman-3-yliden)-methylen]-1,7-diamino-4-methyl-4-aza-heptan. This reaction will need solvent dimethylformamide. The reaction time is 30 minutes at reaction temperature of 80 °C. The yield is about 86%.

N,N-Bis(3-aminopropyl)methylamine can react with 3-Anilinomethylen-2,4-chromandion to get N,N'-Bis-[(2,4-dioxochroman-3-yliden)-methylen]-1,7-diamino-4-methyl-4-aza-heptan

When you are using this chemical, please be cautious about it as the following:
This chemical is harmful if swallowed and can cause burns. And it is toxic by inhalation and in contact with skin During using it, wear suitable protective clothing, gloves and eye/face protection. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. And in case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.).

You can still convert the following datas into molecular structure:
(1)SMILES: NCCCN(CCCN)C
(2)InChI: InChI=1/C7H19N3/c1-10(6-2-4-8)7-3-5-9/h2-9H2,1H3
(3)InChIKey: KMBPCQSCMCEPMU-UHFFFAOYAW

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
rabbit LD50 skin 140uL/kg (0.14mL/kg)   Union Carbide Data Sheet. Vol. 2/28/1967,
rat LC50 inhalation 70mg/m3/4H (70mg/m3) LUNGS, THORAX, OR RESPIRATION: ACUTE PULMONARY EDEMA

LUNGS, THORAX, OR RESPIRATION: DYSPNEA

SKIN AND APPENDAGES (SKIN): HAIR: OTHER		 National Technical Information Service. Vol. OTS0559686,
rat LD50 oral 1540uL/kg (1.54mL/kg)   Union Carbide Data Sheet. Vol. 2/28/1967,

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