Product Name

  • Name

    N,N-DIMETHYL-M-PHENYLENEDIAMINE DIHYDROCHLORIDE

  • EINECS 222-693-0
  • CAS No. 3575-32-4
  • Density 1.049g/cm3
  • Solubility Soluble in water, hot methanol
  • Melting Point 217-220 °C (dec.)
  • Formula C8H12N2.2(HCl)
  • Boiling Point 244.1 °C at 760 mmHg
  • Molecular Weight 209.119
  • Flash Point 88.8 °C
  • Transport Information UN 2811 6.1/PG 2
  • Appearance Off-White Crystalline Solid
  • Safety 36/37/39-45-26
  • Risk Codes 25-36/37/38-43-23/24/25
  • Molecular Structure Molecular Structure of 3575-32-4 (N,N-DIMETHYL-M-PHENYLENEDIAMINE DIHYDROCHLORIDE)
  • Hazard Symbols ToxicT
  • Synonyms 1,3-Benzenediamine,N,N-dimethyl-, dihydrochloride (9CI);m-Phenylenediamine, N,N-dimethyl-, dihydrochloride(8CI);3-Dimethylaminoaniline dihydrochloride;N,N-Dimethyl-1,3-benzenediaminedihydrochloride;N,N-Dimethyl-1,3-phenylenediamine dihydrochloride;N,N-Dimethyl-m-phenylenediamine dihydrochloride;
  • PSA 29.26000
  • LogP 3.52000

Synthetic route

N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

m-dimethylaminoaniline
2836-04-6

m-dimethylaminoaniline

Conditions
ConditionsYield
With sodium carbonate In water at 20℃; for 0.166667h;100%
With sodium hydrogencarbonate In water; ethyl acetate
With potassium carbonate In water3.63 g
di-tert-butyl (2E)-6,6′-bis(4-formylphenyl)-3,3′-dioxo-2,2′-biindole-1,1’(3H,3’H)-dicarboxylate

di-tert-butyl (2E)-6,6′-bis(4-formylphenyl)-3,3′-dioxo-2,2′-biindole-1,1’(3H,3’H)-dicarboxylate

N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

di-tert-butyl (2E)-6,6′-bis[4-((E)-{[3-(dimethylamino)phenyl]imino}methyl)phenyl]-3,3′-dioxo-2,2′-biindole-1,1’(3H,3’H)-dicarboxylate

di-tert-butyl (2E)-6,6′-bis[4-((E)-{[3-(dimethylamino)phenyl]imino}methyl)phenyl]-3,3′-dioxo-2,2′-biindole-1,1’(3H,3’H)-dicarboxylate

Conditions
ConditionsYield
With pyridine In chloroform at -20 - 20℃;90%
3-bromo-8-chloro-imidazo[1,2-a]pyrazine
143591-61-1

3-bromo-8-chloro-imidazo[1,2-a]pyrazine

3,8-dibromo-imidazo[1,2-a]pyrazine
936361-36-3

3,8-dibromo-imidazo[1,2-a]pyrazine

N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

C14H14BrN5
887474-76-2

C14H14BrN5

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In 1-methyl-pyrrolidin-2-one at 160℃; for 18h;77%
8-chloroimidazo[1,2-α]pyrazine
69214-33-1

8-chloroimidazo[1,2-α]pyrazine

8-bromoimidazo[1,2-a]pyrazine
69214-34-2

8-bromoimidazo[1,2-a]pyrazine

N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

C14H14BrN5
887474-76-2

C14H14BrN5

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In 1-methyl-pyrrolidin-2-one at 160℃; for 18h;77%
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

diethyl malonate
105-53-3

diethyl malonate

2,4-dihydroxy-7-(dimethylamino)quinoline
31136-93-3

2,4-dihydroxy-7-(dimethylamino)quinoline

Conditions
ConditionsYield
Stage #1: N,N-dimethyl-1,3-phenylenediamine dihydrochloride With sodium hydroxide In water
Stage #2: diethyl malonate at 200℃; Dean-Stark;
75%
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

diethyl malonate
105-53-3

diethyl malonate

7-(dimethylamino)-4-hydroxyquinolin-2(1H)-one
31136-93-3

7-(dimethylamino)-4-hydroxyquinolin-2(1H)-one

Conditions
ConditionsYield
Stage #1: N,N-dimethyl-1,3-phenylenediamine dihydrochloride With potassium carbonate In water pH=9 - 10;
Stage #2: diethyl malonate In diphenylether Sealed tube; Heating;
74%
tert-Butoxybis(dimethylamino)methane
5815-08-7

tert-Butoxybis(dimethylamino)methane

ethyl 2-(2-ethoxy-2-oxoethyl)-4,5-dimethoxybenzoate

ethyl 2-(2-ethoxy-2-oxoethyl)-4,5-dimethoxybenzoate

N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

2-[3-(dimethylamino)phenyl]-6,7-dimethoxy-1-oxo-1,2-dihydroisoquinoline-4-carboxylic acid

2-[3-(dimethylamino)phenyl]-6,7-dimethoxy-1-oxo-1,2-dihydroisoquinoline-4-carboxylic acid

Conditions
ConditionsYield
Stage #1: tert-Butoxybis(dimethylamino)methane; ethyl 2-(2-ethoxy-2-oxoethyl)-4,5-dimethoxybenzoate at 100℃; for 3h;
Stage #2: N,N-dimethyl-1,3-phenylenediamine dihydrochloride With acetic acid at 20℃; for 2h;
Stage #3: With sodium hydroxide In ethanol at 80℃; for 1h;
70%
4N-hydrogen chloride

4N-hydrogen chloride

(3RS)-1-[(3-Azabicyclo[3.2.2]non-3-yl)carbonylmethyl]-5,9-dimethyl-2,3-dihydro-3-(imidazol-1-yl)carbonylamino-1H-1,4-benzodiazepin-2-one

(3RS)-1-[(3-Azabicyclo[3.2.2]non-3-yl)carbonylmethyl]-5,9-dimethyl-2,3-dihydro-3-(imidazol-1-yl)carbonylamino-1H-1,4-benzodiazepin-2-one

N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

N-[(3RS)-1-(3-azabicyclo[3.2.2]non-3-yl)carbonylmethyl-5,9-dimethyl-2,3-dihydro-2-oxo-1H-1,4-benzodiazepin-3-yl]-N'-[3-(N,N-dimethyl amino)phenyl]urea hydrochloride
206000-79-5

N-[(3RS)-1-(3-azabicyclo[3.2.2]non-3-yl)carbonylmethyl-5,9-dimethyl-2,3-dihydro-2-oxo-1H-1,4-benzodiazepin-3-yl]-N'-[3-(N,N-dimethyl amino)phenyl]urea hydrochloride

Conditions
ConditionsYield
With triethylamine In 1,4-dioxane; water; ethyl acetate; N,N-dimethyl-formamide67.1%
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

N,N-Dimethylcarbamoyl chloride
79-44-7

N,N-Dimethylcarbamoyl chloride

1-(3,3-dimethylureido)-3-(dimethylamino)benzene

1-(3,3-dimethylureido)-3-(dimethylamino)benzene

Conditions
ConditionsYield
Stage #1: N,N-dimethyl-1,3-phenylenediamine dihydrochloride With potassium carbonate In water for 2h;
Stage #2: N,N-Dimethylcarbamoyl chloride With triethylamine In dichloromethane at 0 - 20℃; Schotten-Baumann Reaction; Inert atmosphere;
67%
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

3,5-ditrifluoromethylisocyanate
16588-74-2

3,5-ditrifluoromethylisocyanate

1-(3,5-bis(trifluoromethyl)phenyl)-3-((3-dimethylamino)phenyl)urea
1325760-92-6

1-(3,5-bis(trifluoromethyl)phenyl)-3-((3-dimethylamino)phenyl)urea

Conditions
ConditionsYield
Stage #1: N,N-dimethyl-1,3-phenylenediamine dihydrochloride With sodium hydroxide In dichloromethane; water
Stage #2: 3,5-ditrifluoromethylisocyanate In dichloromethane at 20℃; for 12h;
66%
but-2-ynoic acid [3-cyano-4-(dimethylamino-methyleneamino)-phenyl]-amide
194423-18-2

but-2-ynoic acid [3-cyano-4-(dimethylamino-methyleneamino)-phenyl]-amide

N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

but-2-ynoic acid [4-(3-dimethylamino-phenylamino)-quinazolin-6-yl]-amide

but-2-ynoic acid [4-(3-dimethylamino-phenylamino)-quinazolin-6-yl]-amide

Conditions
ConditionsYield
With potassium carbonate In acetic acid; acetonitrile for 1h; Heating / reflux;58%
N,N-dibenzyl-2,4-dichloro-5,6,7,8-tetrahydroquinazolin-6-amine

N,N-dibenzyl-2,4-dichloro-5,6,7,8-tetrahydroquinazolin-6-amine

N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

N6,N6-dibenzyl-2-chloro-N4-[3-(dimethylamino)phenyl]-5,6,7,8-tetrahydroquinazoline-4,6-diamine

N6,N6-dibenzyl-2-chloro-N4-[3-(dimethylamino)phenyl]-5,6,7,8-tetrahydroquinazoline-4,6-diamine

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In isopropyl alcohol at 100℃; for 6h; Microwave irradiation; Inert atmosphere;56%
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

2,4-dioxo-5-N-(2-fluorophenyl)-1-N-(3-methylbut-1-yl)-3-(phenyloxycarbonylamino)-2,3,4,5-tetrahydro-1H-1,5-benzodiazepine
151620-15-4

2,4-dioxo-5-N-(2-fluorophenyl)-1-N-(3-methylbut-1-yl)-3-(phenyloxycarbonylamino)-2,3,4,5-tetrahydro-1H-1,5-benzodiazepine

N-(3-dimethylaminophenyl)-N'-[2,3,4,5,-tetrahydro-2,4-dioxo-1-(3-methylbutyl)-5-(2-fluorophenyl)-1H-1,5-benzodiazepin-3-yl]urea

N-(3-dimethylaminophenyl)-N'-[2,3,4,5,-tetrahydro-2,4-dioxo-1-(3-methylbutyl)-5-(2-fluorophenyl)-1H-1,5-benzodiazepin-3-yl]urea

Conditions
ConditionsYield
With triethylamine In N,N-dimethyl-formamide at 160℃; for 2h; Condensation;50%
2-chloro-5-nitrobenzoylchloride
25784-91-2

2-chloro-5-nitrobenzoylchloride

N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

sodium hydrogencarbonate
144-55-8

sodium hydrogencarbonate

N-(3-Dimethylamino)phenyl-(2-chloro-5-nitrophenyl)carboxamide
372095-42-6

N-(3-Dimethylamino)phenyl-(2-chloro-5-nitrophenyl)carboxamide

Conditions
ConditionsYield
With pyridine In tetrahydrofuran; ethyl acetate49%
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

glycerol
56-81-5

glycerol

N,N-dimethylquinolin-7-amine
89770-32-1

N,N-dimethylquinolin-7-amine

Conditions
ConditionsYield
Stage #1: N,N-dimethyl-1,3-phenylenediamine dihydrochloride With sodium hydroxide In water
Stage #2: glycerol With sulfuric acid; sodium iodide at 140 - 150℃; for 3h; Skraup Quinoline Synthesis; Cooling with ice;
47%
etanol

etanol

1-(2-toluoylmethyl)-2-oxo-3-amino-5-pivaloyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine
209219-86-3, 209220-79-1, 209220-80-4

1-(2-toluoylmethyl)-2-oxo-3-amino-5-pivaloyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine

N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

1,1'-carbonyldiimidazole
530-62-1

1,1'-carbonyldiimidazole

1-[1-(2-toluoylmethyl)-2-oxo-5-pivaloyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepin-3-yl]-3-[3-(N,N-dimethylamino)phenyl]urea
209218-53-1

1-[1-(2-toluoylmethyl)-2-oxo-5-pivaloyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepin-3-yl]-3-[3-(N,N-dimethylamino)phenyl]urea

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran40.3%
4-chloro-6-(methoxymethyl)-2-(3-methylphenyl)pyrimidine
438249-83-3

4-chloro-6-(methoxymethyl)-2-(3-methylphenyl)pyrimidine

N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

4-(4-Dimethylaminoanilino)-6-(methoxymethyl)-2-(3-methylphenyl)pyrimidine
438247-50-8

4-(4-Dimethylaminoanilino)-6-(methoxymethyl)-2-(3-methylphenyl)pyrimidine

Conditions
ConditionsYield
With hydrogenchloride In water23%
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

4-chloro-6,7-dimethoxyquinoline-3-carbonitrile
214470-55-0

4-chloro-6,7-dimethoxyquinoline-3-carbonitrile

4-(3-dimethylaminophenylamino)-6,7-dimethoxyquinoline-3-carbonitrile hydrochloride

4-(3-dimethylaminophenylamino)-6,7-dimethoxyquinoline-3-carbonitrile hydrochloride

Conditions
ConditionsYield
In 2-ethoxy-ethanol for 3h; Substitution; Heating;18%
2-(2,4-dinitrophenyl)acetyl chloride
109799-62-4

2-(2,4-dinitrophenyl)acetyl chloride

N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

(2,4-dinitro-phenyl)-acetic acid-(3-dimethylamino-anilide)

(2,4-dinitro-phenyl)-acetic acid-(3-dimethylamino-anilide)

Conditions
ConditionsYield
With sodium hydrogencarbonate; benzene
3-(p-nitrophenyl)propanoyl chloride
107324-93-6

3-(p-nitrophenyl)propanoyl chloride

N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

3-(4-nitro-phenyl)-propionic acid-(3-dimethylamino-anilide)

3-(4-nitro-phenyl)-propionic acid-(3-dimethylamino-anilide)

Conditions
ConditionsYield
With sodium hydrogencarbonate; benzene
3-(2,4-dinitro-phenyl)-propionyl chloride
858218-33-4

3-(2,4-dinitro-phenyl)-propionyl chloride

N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

3-(2,4-dinitro-phenyl)-propionic acid-(3-dimethylamino-anilide)
52887-16-8

3-(2,4-dinitro-phenyl)-propionic acid-(3-dimethylamino-anilide)

Conditions
ConditionsYield
With sodium hydrogencarbonate; benzene
potassium cyanate
590-28-3

potassium cyanate

N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

3-ureido-1-dimethylaminobenzene
26455-21-0

3-ureido-1-dimethylaminobenzene

N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

4-nitro-benzoyl chloride
122-04-3

4-nitro-benzoyl chloride

4-nitro-benzoic acid-(3-dimethylamino-anilide)

4-nitro-benzoic acid-(3-dimethylamino-anilide)

Conditions
ConditionsYield
With sodium hydrogencarbonate; benzene
With pyridine; acetone
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

m-nitrobenzoic acid chloride
121-90-4

m-nitrobenzoic acid chloride

3-nitro-benzoic acid-(3-dimethylamino-anilide)

3-nitro-benzoic acid-(3-dimethylamino-anilide)

Conditions
ConditionsYield
With sodium hydrogencarbonate; benzene
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

4-nitrophenylacetyl chloride
50434-36-1

4-nitrophenylacetyl chloride

(4-nitro-phenyl)-acetic acid-(3-dimethylamino-anilide)

(4-nitro-phenyl)-acetic acid-(3-dimethylamino-anilide)

Conditions
ConditionsYield
With sodium hydrogencarbonate; benzene
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

3,5-dinitrobenoyl chloride
99-33-2

3,5-dinitrobenoyl chloride

3,5-dinitro-benzoic acid-(3-dimethylamino-anilide)
108299-43-0

3,5-dinitro-benzoic acid-(3-dimethylamino-anilide)

Conditions
ConditionsYield
With sodium hydrogencarbonate; benzene
4-Acetyl-phenyl-diazonium
19262-73-8

4-Acetyl-phenyl-diazonium

N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

1-[4-(2-Amino-4-dimethylamino-phenylazo)-phenyl]-ethanone

1-[4-(2-Amino-4-dimethylamino-phenylazo)-phenyl]-ethanone

N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

4-Hydroxymethyl-benzenediazonium
78246-53-4

4-Hydroxymethyl-benzenediazonium

[4-(2-Amino-4-dimethylamino-phenylazo)-phenyl]-methanol

[4-(2-Amino-4-dimethylamino-phenylazo)-phenyl]-methanol

thiophosgene
463-71-8

thiophosgene

N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

3-N,N-dimethylaminophenylisothiocyanate
2392-67-8

3-N,N-dimethylaminophenylisothiocyanate

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In toluene at 75℃;
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3575-32-4

N,N-dimethyl-1,3-phenylenediamine dihydrochloride

1-(2-cyclopentylethyl)-2,4-dioxo-5-(2-fluorophenyl)-3-isocyanato-2,3,4,5-tetrahydro-1H-1,5-benzodiazepine
153930-53-1

1-(2-cyclopentylethyl)-2,4-dioxo-5-(2-fluorophenyl)-3-isocyanato-2,3,4,5-tetrahydro-1H-1,5-benzodiazepine

1-[1-(2-cyclopentyl-ethyl)-5-(2-fluoro-phenyl)-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl]-3-(3-dimethylamino-phenyl)-urea

1-[1-(2-cyclopentyl-ethyl)-5-(2-fluoro-phenyl)-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl]-3-(3-dimethylamino-phenyl)-urea

Conditions
ConditionsYield
In acetonitrile for 7h; Addition;

N,N-Dimethyl-1,3-phenylenediamine dihydrochloride Specification

The cas register number of N,N-Dimethyl-1,3-phenylenediamine dihydrochloride is 3575-32-4. It also can be called as N,N-Dimethyl-m-phenylenediamine dihydrochloride and the IUPAC Name about this chemical is 3-N,3-N-dimethylbenzene-1,3-diamine dihydrochloride. It belongs to the following product categories, such as Aromatics Compounds, Aromatics and so on.

Physical properties about N,N-Dimethyl-1,3-phenylenediamine dihydrochloride are: (1)ACD/LogP: 1.05; (2)ACD/LogD (pH 5.5): 0.9; (3)ACD/LogD (pH 7.4): 1.04; (4)ACD/BCF (pH 5.5): 2.64; (5)ACD/BCF (pH 7.4): 3.65; (6)ACD/KOC (pH 5.5): 63.51; (7)ACD/KOC (pH 7.4): 87.81; (8)#H bond acceptors: 2; (9)#H bond donors: 2; (10)#Freely Rotating Bonds: 2; (11)Polar Surface Area: 6.48Å2; (12)Flash Point: 88.8 °C; (13)Enthalpy of Vaporization: 48.11 kJ/mol; (14)Boiling Point: 244.1 °C at 760 mmHg; (15)Vapour Pressure: 0.0309 mmHg at 25°C.

When you are using this chemical, please be cautious about it as the following:
This chemical is toxic by inhalation, in contact with skin and if swallowed and it is irritating to eyes, respiratory system and skin, it also may cause sensitization by skin contact. When you are 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)Canonical SMILES: CN(C)C1=CC=CC(=C1)N.Cl.Cl
(2)InChI: InChI=1S/C8H12N2.2ClH/c1-10(2)8-5-3-4-7(9)6-8;;/h3-6H,9H2,1-2H3;2*1H
(3)InChIKey: BZJPIQKDEGXVFG-UHFFFAOYSA-N

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