CAS No.3058-38-6,2,4,6-trinitrobenzene-1,3,5-triamine Suppliers

Ality Chemical Corporation

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2,4,6-trinitrobenzene-1,3,5-triamine CAS:3058-38-6 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quali

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Zibo Hangyu Biotechnology Development Co., Ltd

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Henan Tianfu Chemical Co., Ltd.

2,4,6-trinitrobenzene-1,3,5-triamine;sym-Triaminotrinitrobenzene; 1,3,5-Trinitro-2,4,6-triaminobenzene; 2,4,6-Trinitro-1,3,5- Benzenetriamine; TATB; s-TriaMinotrinitrobenzene; EDC 35; NSC 243156 CAS No.: 3058-38-6 Molecular formula: C6H6N6O6

2,4,6-trinitrobenzene-1,3,5-triamine

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Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali

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Hangzhou Fandachem Co.,Ltd

1,3,5-Triamino-2,4,6-trinitrobenzene cas 3058-38-6Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express

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Henan Kanbei Chemical Co.,LTD

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Shanghai Yuanye Bio-Technology Co., Ltd.

Known for its best quality and competitve price, this chemicals we offered is widely appreciated by our customers.Appearance:White powder Storage:keep sealed and keep from direct light Package:According client's requirements Application:pharmaceutica

s-Triaminotrinitrobenzene manufacturer

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ZHEJIANG JIUZHOU CHEM CO.,LTD

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HuBei Ipure Biotech CO.,ltd

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Shanghai united Scientific Co.,Ltd.

United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat

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Finetech Industry Limited

FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the s-Triaminotrinitrobenzene, CAS:3058-38-6 with the most competitive price and the best

s-Triaminotrinitrobenzene

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Nanjing Raymon Biotech Co., Ltd.

s-TriaminotrinitrobenzeneAppearance:White Storage:keep in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/pharma intermediate Transportation:By Sea,by Air,By courier like DHL or Fedx. Port:Shanghai/S

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Synthetic route

: 489-98-5
picramide

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
With 4-amino-1,2,4-triazole; sodium methylate In methanol at 25 - 60℃; for 21.5h; Product distribution / selectivity;	99.8%
Stage #1: picramide With 4-amino-1,2,4-triazole; sodium methylate In methanol; toluene at 25 - 60℃; for 16.5h; Stage #2: With acetic acid In methanol; toluene Product distribution / selectivity;	98%
With 4-amino-1,2,4-triazole; sodium methylate In dimethyl sulfoxide at 20℃; for 3h;	94.1%

: C30H27N9O12

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
With hydrogenchloride In water; dimethyl sulfoxide at 80℃; for 6h; pH=1;	99.6%

: 68959-41-1
1,3,5-triethoxy-2,4,6-trinitrobenzene

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
With ammonia In toluene at 90℃; under 3863.02 Torr; for 4h; Product distribution / selectivity;	99.5%
With methanol; ammonia at -3 - 50℃; for 24h; Product distribution / selectivity; Sealed reactor; Industry scale;	89.5%

: C27H18Cl3N9O9

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
With sodium hydroxide In water; dimethyl sulfoxide at 65℃; for 8h; pH=13.5;	99.5%

: C30H18F9N9O9

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
With sodium hydroxide In water; dimethyl sulfoxide at 65℃; for 5h; pH=14;	99.4%

: C33H36N12O9

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
With sodium hydroxide In water; dimethyl sulfoxide at 60℃; for 5h; pH=14;	99.4%

: C30H27N9O9

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
With sodium hydroxide In water; dimethyl sulfoxide at 60℃; for 6h; pH=14;	99.2%

: 2631-68-7
1,3,5-trichloro-2,4,6-trinitrobenzene

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
With ammonia In toluene for 10h; Heating;	99%
With ammonia	90%
With ammonia In toluene for 24h; Reflux;	87%

: 21985-87-5
2,3,4,5,6-pentanitroaniline 1,2-dichloroethane

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
With ammonia In tetrachloromethane; toluene for 0.583333h;	97%
With ammonia

: 584-13-4
4-amino-1,2,4-triazole

: 489-98-5
picramide

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
With sodium methylate In dimethyl sulfoxide at 20℃; for 3h;	89.5%

: 489-98-5
picramide

: 5470-11-1
hydroxylamine hydrochloride

A: 439614-66-1
1,3,5-triamino-2,4-dinitro-6-nitrososbenzene

B: 1630-08-6
1,3,5-trinitrobenzenediamine

C: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
Stage #1: picramide; hydroxylamine hydrochloride With sodium methylate In methanol; dimethyl sulfoxide; toluene at 25 - 90℃; for 2.33333h; Stage #2: With acetic acid In dimethyl sulfoxide; toluene Product distribution / selectivity;	A n/a B n/a C 85%

...Expand

: 56140-58-0
1,3-diamino-5-hydroxytrinitrobenzene

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
With diammonium phosphate In sulfolane at 20 - 177℃; for 8h;	80%

: 172265-85-9
2,4,6-trinitro-1,3,5-triacetylaminobenzene

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
With hydrogenchloride In water at 100℃; for 0.5h; Temperature; Reagent/catalyst;	77.5%
With ammonia In water; N,N-dimethyl-formamide at 20 - 130℃; under 8791.75 Torr; for 0.666667 - 2.5h; Product distribution / selectivity;	68%
With ammonia In water at 123℃; for 1h;	58%

: 83430-12-0
1,3,5-tribromo-2,4,6-trinitrobenzene

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
With ammonia In toluene	72%

: Ac3TADNB

: 88106-06-3
N,N'-Diacetyl-2,4-diamino-1,3,5-trinitrobenzene

: 172265-85-9
2,4,6-trinitro-1,3,5-triacetylaminobenzene

A: 439614-66-1
1,3,5-triamino-2,4-dinitro-6-nitrososbenzene

B: 1630-08-6
1,3,5-trinitrobenzenediamine

C: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
With ammonia In water at 123℃; for 1h;	A n/a B n/a C 62%

...Expand

: 26243-62-9
N,N',N”-triacetyl-1,3,5-triaminobenzene

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
Stage #1: N,N',N”-triacetyl-1,3,5-triaminobenzene With nitric acid; acetic anhydride at -5℃; for 8h; Stage #2: With nitric acid; acetic anhydride In water at 20 - 105℃; for 17h; Reagent/catalyst; Temperature; Solvent;	56%
Multi-step reaction with 2 steps 1: nitric acid; sulfuric acid / 0.25 h / -5 - 25 °C 2: hydrogenchloride / water / 0.5 h / 100 °C View Scheme
Multi-step reaction with 3 steps 1.1: nitric acid; sulfuric acid / 4 h / 50 °C / Cooling with ice 2.1: water / 6 h / 95 °C / Cooling with ice 3.1: acetic anhydride / 2 h / Cooling with ice 3.2: 8 h / 40 °C View Scheme

: 1423-11-6
1,3,5-trifluoro-2,4,6-trinitrobenzene

A: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

B: 73333-89-8
1-amino-3,5-difluorotrinitrobenzene

C: 78925-50-5
3,5-diamino-1-fluoro-2,4,6-trinitrobenzene

Conditions

Conditions	Yield
With ammonia In dichloromethane at -73℃; for 1h; Yields of byproduct given;	A 0.22 g B n/a C n/a
With ammonia In dichloromethane at -73℃; for 1h; Yield given. Yields of byproduct given;

...Expand

: 1423-11-6
1,3,5-trifluoro-2,4,6-trinitrobenzene

A: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

B: 78925-50-5
3,5-diamino-1-fluoro-2,4,6-trinitrobenzene

Conditions

Conditions	Yield
With potassium hydrogencarbonate; tert-butylamine; trifluoroacetic acid 1.) CH2Cl2, -30 deg C, 2.) room temperature, 15h, 3.) 20 h; Yield given. Multistep reaction. Yields of byproduct given;

2.4.6-tribromo-1.3.5-triamino-benzene: 2.4.6-tribromo-1.3.5-triamino-benzene

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
With ethanol; ammonia in der Siedehitze;

: 2631-68-7
1,3,5-trichloro-2,4,6-trinitrobenzene

: 7664-41-7
ammonia

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

: 83430-12-0
1,3,5-tribromo-2,4,6-trinitrobenzene

: 7664-41-7
ammonia

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

: 21985-87-5
2,3,4,5,6-pentanitroaniline 1,2-dichloroethane

ammonia <10 percent >: ammonia <10 percent >

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

: 35572-78-2
2-amino-4,6-dinitrotoluene

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: 80percent aq. H2SO4, 90percent aq. nitric acid / 24 h / Ambient temperature 2: 78 percent / 96percent aq. H2SO4, anisole / 0.5 h / Ambient temperature 3: 40 percent / 90percent HNO3, 100percent H2SO4 / 1.) RT, 60 min, 2.) 75 deg C, 90 min 4: 97 percent / anh. ammonia / toluene; CCl4 / 0.58 h View Scheme

: 19406-51-0
4-Amino-2,6-dinitrotoluene

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: 78 percent / 96percent H2SO4, 90percent HNO3 / acetic acid / 9 h / 0 °C 2: 35 percent / 96percent aq. H2SO4 / 60 h / 0 °C 3: 40 percent / 90percent HNO3, 100percent H2SO4 / 1.) RT, 60 min, 2.) 75 deg C, 90 min 4: 97 percent / anh. ammonia / toluene; CCl4 / 0.58 h View Scheme
Multi-step reaction with 4 steps 1: 100 percent / 96percent aq. H2SO4, 90percent aq. HNO3 / 16 h / 0 - 5 °C 2: 78 percent / 96percent aq. H2SO4, anisole / 0.5 h / Ambient temperature 3: 40 percent / 90percent HNO3, 100percent H2SO4 / 1.) RT, 60 min, 2.) 75 deg C, 90 min 4: 97 percent / anh. ammonia / toluene; CCl4 / 0.58 h View Scheme

: 84432-53-1
4-Amino-2,3,5,6-tetranitrotoluene

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 40 percent / 90percent HNO3, 100percent H2SO4 / 1.) RT, 60 min, 2.) 75 deg C, 90 min 2: 97 percent / anh. ammonia / toluene; CCl4 / 0.58 h View Scheme

: 84432-52-0
4-amino-N,2,3,6-tetranitrotoluene

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 35 percent / 96percent aq. H2SO4 / 60 h / 0 °C 2: 40 percent / 90percent HNO3, 100percent H2SO4 / 1.) RT, 60 min, 2.) 75 deg C, 90 min 3: 97 percent / anh. ammonia / toluene; CCl4 / 0.58 h View Scheme

: 84432-54-2
4-amino-N,2,3,5,6-pentanitrotoluene

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 78 percent / 96percent aq. H2SO4, anisole / 0.5 h / Ambient temperature 2: 40 percent / 90percent HNO3, 100percent H2SO4 / 1.) RT, 60 min, 2.) 75 deg C, 90 min 3: 97 percent / anh. ammonia / toluene; CCl4 / 0.58 h View Scheme

: 618-87-1
3, 5-dinitroaniline

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: sulfuric acid <100 percent >; nitric acid / 75 °C 2: ammonia View Scheme

: 18523-16-5
1,3,5-Trimethoxy-2,4,6-trinitrobenzene

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

Conditions

Conditions	Yield
With ammonia In diethyl ether
With ammonia In ethyl acetate under 760.051 Torr; for 6h;

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

: 4444-26-2
benzenehexamine

Conditions

Conditions	Yield
With ammonia; sodium In methanol Heating;	95%
With hydrogen; palladium on activated charcoal In ethyl acetate	80%
With phenylhydrazine 1.) 120 degC, 2.5 h; 2.) to 140 degC in 2.5 h; 3.) 140 degC, 1h;	68%

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

: hexaamino-benzene trihydrochloride

Conditions

Conditions	Yield
Stage #1: 2,4,6-triamino-1,3,5-trinitrobenzene With palladium 10% on activated carbon; hydrogen In ethyl acetate under 3150.32 Torr; for 72h; Stage #2: With hydrogenchloride	93.2%
Stage #1: 2,4,6-triamino-1,3,5-trinitrobenzene With palladium 10% on activated carbon; hydrogen In ethyl acetate under 3150.32 Torr; for 72h; Stage #2: With hydrogenchloride; palladium 10% on activated carbon; hydrogen In water; ethyl acetate under 3150.32 Torr; for 5h;	92%
Stage #1: 2,4,6-triamino-1,3,5-trinitrobenzene With palladium 10% on activated carbon; hydrogen In ethyl acetate under 3150.32 Torr; for 72h; Stage #2: With hydrogenchloride; hydrogen In water; ethyl acetate for 5h;	92%
With hydrogenchloride; tin(II) chloride dihdyrate In ethyl acetate for 5h; Reflux;	75%

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

: 108-24-7
acetic anhydride

: 172265-85-9
2,4,6-trinitro-1,3,5-triacetylaminobenzene

Conditions

Conditions	Yield
sulfuric acid at 20 - 98℃; for 5h; Product distribution / selectivity;	93%
With sulfuric acid at 115 - 120℃; for 28h;	85.3%

: 67-56-1
methanol

: 3153-26-2
bis(acetylacetonate)oxovanadium

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

: 68-12-2, 33513-42-7
N,N-dimethyl-formamide

: [NH2Me2]4{[V6O6(OCH3)9(VO4)]4(1,3,5-triamido-2,4,6-trinitrobenzene)4}·(MeOH)24

Conditions

Conditions	Yield
at 160℃; for 48h; Autoclave;	80%

...Expand

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

: 135285-90-4
2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurzitane

: 3C6H6N12O12*C6H6N6O6

Conditions

Conditions	Yield
In water for 1.5h;	75.5%

: 67-56-1
methanol

: oxovanadium(IV) sulfate

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

: 68-12-2, 33513-42-7
N,N-dimethyl-formamide

: [NH2Me2]8{[V6O6(OCH3)9(SO4)]4(1,3,5-triamido-2,4,6-trinitrobenzene)4}·(MeOH)9

Conditions

Conditions	Yield
at 160℃; for 48h; Autoclave;	65%

...Expand

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

: hexaaminobenzene tetrahydrochloride

Conditions

Conditions	Yield
With hydrogenchloride; tin(ll) chloride In water at 20℃; for 48h; Inert atmosphere; Schlenk technique;	64%

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

: 4328-17-0
trinitrophloroglucinol

Conditions

Conditions	Yield
With sodium hydroxide

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

: 608-97-9
benzenepentamine

Conditions

Conditions	Yield
With hydrogenchloride; tin

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

: 100-63-0
phenylhydrazine

: 4444-26-2
benzenehexamine

Conditions

Conditions	Yield
at 140 - 200℃;
at 140℃; dann bei 200grad;

: 4443-63-4
icosane-10,11-dione

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

A: 120829-14-3
5-Amino-6-nitro-2,3,8,9-tetranonylpyrazino<2,3-f>quinoxaline

B: 96355-62-3
2,3,6,7,10,11-hexanonyldipyrazino<2,3-f;2',3'-h>quinoxaline

Conditions

Conditions	Yield
With hydrogen; palladium on activated charcoal 1.) ethyl acetate, 2.) ethanol, glacial acetic acid, H2O, 50 deg C, 1.5 h; Yield given. Multistep reaction. Yields of byproduct given;

...Expand

: 3058-38-6
2,4,6-triamino-1,3,5-trinitrobenzene

A: 4444-26-2
benzenehexamine

B: 120829-15-4
nitrobenzenepentamine

Conditions

Conditions	Yield
With hydrogen; palladium on activated charcoal In ethyl acetate

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305-84-0

L-Carnosine

3058-47-7

1-Methylsulfanyl-2-nitro-benzene

305-85-1

Phenol,2,6-diiodo-4-nitro-

305851-04-1

1-Benzotriazol-1-yl-3-chloropropan-2-one

305858-63-3

Hexanoic acid, 6-[[4-(1-methylethoxy)benzoyl]amino]-

30586-13-1

Benzenesulfonic acid,[[4-[(4-amino-3-methylphenyl)hydroxy[4-(phenylamino)phenyl]methyl]phenyl]amino]-,sodium salt (1:1)

30586-93-7

Acrylic acid, 2-ethylhexyl ester, polymer with acrylonitrile and N-(hydroxymethyl)-2-methylacrylamide

3058-98-8

1-Naphthalenesulfonicacid, 4-hydroxy-3-[2-[4-methyl-3-[(phenylamino)sulfonyl]phenyl]diazenyl]-,sodium salt (1:1)

3059-67-4

N-methylpyrimidine-4,5-diamine

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