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CAS

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1,3-Diaminoguanidine monohydrochloride is an organic compound that is widely utilized in various industries due to its unique chemical properties. It is known for undergoing condensation reactions with different compounds, such as 4-isothiocyanato-4-methylpentane-2-one and various aldehydes and ketones, to produce a range of products including condensed pyrimidines and bis guanidine derivatives.

36062-19-8

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36062-19-8 Usage

Uses

Used in Analytical Chemistry:
1,3-Diaminoguanidine monohydrochloride is used as an analyte for High-Performance Liquid Chromatography (HPLC) due to its compatibility with the technique and its ability to provide accurate and reliable results in the analysis of complex samples.
Used in Energetic Materials Synthesis:
1,3-Diaminoguanidine monohydrochloride is used as an intermediate for the synthesis of energetic salts or materials based on dinitroguanidine. Its role in the production process is crucial, as it contributes to the development of advanced materials with enhanced performance characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 36062-19-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,6 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 36062-19:
(7*3)+(6*6)+(5*0)+(4*6)+(3*2)+(2*1)+(1*9)=98
98 % 10 = 8
So 36062-19-8 is a valid CAS Registry Number.

36062-19-8 Well-known Company Product Price

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  • Detail
  • Alfa Aesar

  • (B22615)  N,N'-Diaminoguanidine monohydrochloride, 98%   

  • 36062-19-8

  • 5g

  • 320.0CNY

  • Detail
  • Alfa Aesar

  • (B22615)  N,N'-Diaminoguanidine monohydrochloride, 98%   

  • 36062-19-8

  • 25g

  • 1004.0CNY

  • Detail
  • Alfa Aesar

  • (B22615)  N,N'-Diaminoguanidine monohydrochloride, 98%   

  • 36062-19-8

  • 100g

  • 2917.0CNY

  • Detail
  • Aldrich

  • (143413)  1,3-Diaminoguanidinemonohydrochloride  98%

  • 36062-19-8

  • 143413-25G

  • 898.56CNY

  • Detail

36062-19-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-Diaminoguanidine monohydrochloride

1.2 Other means of identification

Product number -
Other names N,N'-DIAMINOGUANIDINE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:36062-19-8 SDS

36062-19-8Synthetic route

cyanogen chloride
506-77-4

cyanogen chloride

1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

Conditions
ConditionsYield
With diethyl ether; hydrazine
With hydrazine In water in NaCl saturated water;
With hydrazine In gas with hydrazine free from water and layered with ether; hydrazine cooled;
With hydrazine In water ClCN/H2N-NH2 = 1:2;
With hydrazine In water in NaCl saturated water;
cyanogen chloride
506-77-4

cyanogen chloride

A

1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

B

hydrochloride of guanazine

hydrochloride of guanazine

Conditions
ConditionsYield
With water; hydrazine Nebenprod.2:Hydrazin-N.N'-dicarbonsaeure-amid-hydrazid;
guanidine hydrochloride salt

guanidine hydrochloride salt

1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

Conditions
ConditionsYield
With hydrazine hydrate In water; chlorobenzene at 25℃; for 10h; Time;
1-aminoguanidine hydrochloride
1937-19-5

1-aminoguanidine hydrochloride

1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

Conditions
ConditionsYield
With hydrazine
1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

4-nitrobenzaldehdye
555-16-8

4-nitrobenzaldehdye

2,2'-bis[(4-nitrophenyl)methylene]carbonimidic dihydrazide monohydrochloride
473391-26-3

2,2'-bis[(4-nitrophenyl)methylene]carbonimidic dihydrazide monohydrochloride

Conditions
ConditionsYield
In ethanol for 16h; Reflux;100%
In ethanol at 100℃; for 0.166667h; Microwave irradiation;81%
In methanol at 20 - 80℃; for 26h;75%
1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

2,2′-bis[(3-chlorophenyl)methylene]carbonimidic dihydrazide monohydrochloride

2,2′-bis[(3-chlorophenyl)methylene]carbonimidic dihydrazide monohydrochloride

Conditions
ConditionsYield
In ethanol for 16h; Reflux;100%
In ethanol for 16h; Reflux;
1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

ortho-bromobenzaldehyde
6630-33-7

ortho-bromobenzaldehyde

2,2′-bis[(2-bromophenyl)methylene]carbonimidic dihydrazide monohydrochloride

2,2′-bis[(2-bromophenyl)methylene]carbonimidic dihydrazide monohydrochloride

Conditions
ConditionsYield
In ethanol for 16h; Reflux;100%
In ethanol at 100℃; for 0.166667h; Microwave irradiation;72%
4-Trifluoromethylbenzaldehyde
455-19-6

4-Trifluoromethylbenzaldehyde

1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

2,2′-bis[(4-(trifluoromethyl)phenyl)methylene]carbonimidic dihydrazide monohydrochloride
57401-20-4

2,2′-bis[(4-(trifluoromethyl)phenyl)methylene]carbonimidic dihydrazide monohydrochloride

Conditions
ConditionsYield
In ethanol for 16h; Reflux;100%
In ethanol for 16h; Reflux;
1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

4-hydroxy-benzaldehyde
123-08-0

4-hydroxy-benzaldehyde

2,2′-bis[(4-hydroxyphenyl)methylene]carbonimidic dihydrazide monohydrochloride

2,2′-bis[(4-hydroxyphenyl)methylene]carbonimidic dihydrazide monohydrochloride

Conditions
ConditionsYield
In ethanol for 16h; Reflux;100%
In ethanol at 100℃; for 0.166667h; Microwave irradiation;18%
1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

4-Phenylbenzaldehyde
3218-36-8

4-Phenylbenzaldehyde

2,2′-bis[(1,1'-biphenyl-4-yl)methylene]carbonimidic dihydrazide monohydrochloride

2,2′-bis[(1,1'-biphenyl-4-yl)methylene]carbonimidic dihydrazide monohydrochloride

Conditions
ConditionsYield
In ethanol for 16h; Reflux;100%
In ethanol at 100℃; for 0.166667h; Microwave irradiation;81%
1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

3,4-dimethoxy-benzaldehyde
120-14-9

3,4-dimethoxy-benzaldehyde

2,2′-bis[(3,4-dimethoxyphenyl)methylene]carbonimidic dihydrazide monohydrochloride

2,2′-bis[(3,4-dimethoxyphenyl)methylene]carbonimidic dihydrazide monohydrochloride

Conditions
ConditionsYield
In ethanol at 100℃; for 0.166667h; Microwave irradiation;100%
1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

4-cyanobenzaldehyde
105-07-7

4-cyanobenzaldehyde

2,2'-bis[(4-cyanophenyl)methylene]carbonimidic dihydrazide monohydrochloride

2,2'-bis[(4-cyanophenyl)methylene]carbonimidic dihydrazide monohydrochloride

Conditions
ConditionsYield
In ethanol for 16h; Reflux;100%
In ethanol for 16h; Reflux;
3-Cyanobenzaldehyde
24964-64-5

3-Cyanobenzaldehyde

1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

2,2'-bis[(3-cyanophenyl)methylene]carbonimidic dihydrazide monohydrochloride

2,2'-bis[(3-cyanophenyl)methylene]carbonimidic dihydrazide monohydrochloride

Conditions
ConditionsYield
In ethanol for 16h; Reflux;100%
In ethanol for 16h; Reflux;
1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

2-(trifluoromethoxy)benzaldehyde
94651-33-9

2-(trifluoromethoxy)benzaldehyde

2,2'-bis[(2-trifluoromethoxyphenyl)methylene]-carbonimidic dihydrazide hydrochloride

2,2'-bis[(2-trifluoromethoxyphenyl)methylene]-carbonimidic dihydrazide hydrochloride

Conditions
ConditionsYield
In ethanol for 16h; Reflux;100%
1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

4-difluoromethoxy-acetophenone
83882-67-1

4-difluoromethoxy-acetophenone

2,2'-bis[(4-difluoromethoxyphenyl)ethylidene]-carbonimidic dihydrazide hydrochloride

2,2'-bis[(4-difluoromethoxyphenyl)ethylidene]-carbonimidic dihydrazide hydrochloride

Conditions
ConditionsYield
In ethanol for 16h; Reflux;100%
4-formylbenzamide
6051-41-8

4-formylbenzamide

1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

C17H17N7O2*ClH

C17H17N7O2*ClH

Conditions
ConditionsYield
In ethanol for 16h; Reflux;100%
4-formyl-benzenesulfonamide
3240-35-5

4-formyl-benzenesulfonamide

1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

C15H17N7O4S2*ClH

C15H17N7O4S2*ClH

Conditions
ConditionsYield
In ethanol for 16h; Reflux;100%
4-propynoxybenzaldehyde

4-propynoxybenzaldehyde

1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

2,2'-bis[(4-propynoxyphenyl)methylene]carbonimidic dihydrazide hydrochloride

2,2'-bis[(4-propynoxyphenyl)methylene]carbonimidic dihydrazide hydrochloride

Conditions
ConditionsYield
In ethanol for 16h; Reflux;100%
silver 1,1'-ethylenebis(oxy)bis(5-nitroiminotetrazolate)

silver 1,1'-ethylenebis(oxy)bis(5-nitroiminotetrazolate)

1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

2CH7N5*C4H6N12O6

2CH7N5*C4H6N12O6

Conditions
ConditionsYield
In water at 20℃; for 4h;99%
1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

benzaldehyde
100-52-7

benzaldehyde

2,2′-bis[phenylmethylene]carbonimidic dihydrazide monohydrochloride
72463-09-3

2,2′-bis[phenylmethylene]carbonimidic dihydrazide monohydrochloride

Conditions
ConditionsYield
In ethanol for 16h; Reflux;99%
In ethanol at 100℃; for 0.166667h; Microwave irradiation;88%
In ethanol; water at 20 - 80℃; for 2h;65%
In methanol at 20 - 80℃; for 26h;64%
silver 1-methoxy-5-nitroiminotetrazolate

silver 1-methoxy-5-nitroiminotetrazolate

1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

1,3-diaminoguanidinium 1-methoxy-5-nitroiminotetrazolate
1428559-67-4

1,3-diaminoguanidinium 1-methoxy-5-nitroiminotetrazolate

Conditions
ConditionsYield
In water at 20℃; for 3h; Thermodynamic data;99%
1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

4-fluorobenzaldehyde
459-57-4

4-fluorobenzaldehyde

2,2′-bis[(4-fluorophenyl)methylene]carbonimidic dihydrazide monohydrochloride

2,2′-bis[(4-fluorophenyl)methylene]carbonimidic dihydrazide monohydrochloride

Conditions
ConditionsYield
In ethanol for 16h; Reflux;99%
In ethanol for 16h; Reflux;
1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

2-Fluorobenzaldehyde
446-52-6

2-Fluorobenzaldehyde

2,2′-bis[(2-fluorophenyl)methylene]carbonimidic dihydrazide monohydrochloride

2,2′-bis[(2-fluorophenyl)methylene]carbonimidic dihydrazide monohydrochloride

Conditions
ConditionsYield
In ethanol for 16h; Reflux;99%
In ethanol for 16h; Reflux;
1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

2-fluoro-5-formylbenzonitrile
218301-22-5

2-fluoro-5-formylbenzonitrile

2,2'-bis[(3-cyano-4-fluorophenyl)methylene]-carbonimidic dihydrazide hydrochloride

2,2'-bis[(3-cyano-4-fluorophenyl)methylene]-carbonimidic dihydrazide hydrochloride

Conditions
ConditionsYield
In ethanol for 16h; Reflux;99%
1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

4-chlorobenzaldehyde
104-88-1

4-chlorobenzaldehyde

2,2′-bis[(4-chlorophenyl)methylene]carbonimidic dihydrazide monohydrochloride
25875-50-7

2,2′-bis[(4-chlorophenyl)methylene]carbonimidic dihydrazide monohydrochloride

Conditions
ConditionsYield
With hydrogenchloride In methanol at 50℃; for 1h; pH=1.5; pH-value; Temperature;98.82%
In ethanol for 16h; Reflux;
5-nitro-2-thiophenecarboxaldehyde
4521-33-9

5-nitro-2-thiophenecarboxaldehyde

1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

1,3-bis-((5-nitrothiophen-2-yl-methylidene)amino)guanidine hydrochloride
1206770-32-2

1,3-bis-((5-nitrothiophen-2-yl-methylidene)amino)guanidine hydrochloride

Conditions
ConditionsYield
In methanol for 5h; Reflux;98%
1,1,3,6,8,8-Hexanitro-3,6-diaza-octan
41792-58-9

1,1,3,6,8,8-Hexanitro-3,6-diaza-octan

1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

bis(2,2-dinitroethanide-N-nitro)ethylenediamine bis(diaminoguanidinium) salt

bis(2,2-dinitroethanide-N-nitro)ethylenediamine bis(diaminoguanidinium) salt

Conditions
ConditionsYield
Stage #1: 1,3-diaminoguanidine hydrochloride With sodium hydroxide In methanol at 20℃; for 0.166667h;
Stage #2: 1,1,3,6,8,8-Hexanitro-3,6-diaza-octan In acetonitrile at 20℃; for 1h;
98%
m-bromobenzoic aldehyde
3132-99-8

m-bromobenzoic aldehyde

1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

2,2′-bis[(3-bromophenyl)methylene]carbonimidic dihydrazide monohydrochloride

2,2′-bis[(3-bromophenyl)methylene]carbonimidic dihydrazide monohydrochloride

Conditions
ConditionsYield
In ethanol for 16h; Reflux;98%
In ethanol at 100℃; for 0.166667h; Microwave irradiation;44%
1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

sodium 3,6-dinitro-2,5-dihydroxy-1,4-benzoquinone
5357-76-6

sodium 3,6-dinitro-2,5-dihydroxy-1,4-benzoquinone

N,N'-diaminoguanidinium nitranilate

N,N'-diaminoguanidinium nitranilate

Conditions
ConditionsYield
In water at 20℃;97%
1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

Dipikrylamin
131-73-7

Dipikrylamin

CH7N5*C12H5N7O12
1352994-43-4

CH7N5*C12H5N7O12

Conditions
ConditionsYield
Stage #1: Dipikrylamin With sodium hydroxide In water at 80℃; for 0.5h;
Stage #2: 1,3-diaminoguanidine hydrochloride In water at 20℃; for 1h;
97%
1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

3-Fluorobenzaldehyde
456-48-4

3-Fluorobenzaldehyde

2,2′-bis[(3-fluorophenyl)methylene]carbonimidic dihydrazide monohydrochloride

2,2′-bis[(3-fluorophenyl)methylene]carbonimidic dihydrazide monohydrochloride

Conditions
ConditionsYield
In ethanol for 16h; Reflux;97%
In ethanol for 16h; Reflux;
1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

CH7N5*HN3O4

CH7N5*HN3O4

Conditions
ConditionsYield
With silver(I) dinitramide In ethanol96%
methyl (4-pyridyl) ketone
1122-54-9

methyl (4-pyridyl) ketone

1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

1,3-bis-((1-(4-pyridyl)ethylidene)amino)guanidine hydrochloride
1206770-40-2

1,3-bis-((1-(4-pyridyl)ethylidene)amino)guanidine hydrochloride

Conditions
ConditionsYield
In methanol for 5h; Reflux;96%
1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

2-chloro-benzaldehyde
89-98-5

2-chloro-benzaldehyde

2,2′-bis[(2-chlorophenyl)methylene]carbonimidic dihydrazide monohydrochloride

2,2′-bis[(2-chlorophenyl)methylene]carbonimidic dihydrazide monohydrochloride

Conditions
ConditionsYield
In ethanol for 16h; Reflux;96%
In ethanol for 16h; Reflux;

36062-19-8Relevant articles and documents

A facile synthesis of energetic salts based on fully nitroamino-functionalized [1,2,4]triazolo[4,3-b] [1,2,4]triazole

Bian, Chengming,Feng, Wenjing,Lei, Qunying,Huang, Haifeng,Li, Xia,Wang, Jianlong,Li, Chuan,Xiao, Zhongliang

, p. 368 - 374 (2020)

A novel family of fully nitroamino-functionalized [1,2,4]triazolo[4,3-b][1,2,4]triazole-based energetic salts were synthesized. All salts were characterized by IR and multinuclear NMR spectroscopy, thermal analysis and elemental analysis. The crystal structures of salts 5, 6, and 7 were confirmed by single-crystal X-ray diffraction. The densities of these salts are between 1.65 (4) and 1.89 g cm-3 (3), whilst their oxygen balances are between -42.8% (7) and -11.3% (3). Theoretical performance calculations (Gaussian 09 and EXPLO 6.01) provided detonation pressures and velocities for salts 2-7 in the ranges of 27.6-41.1 GPa and 8519-9518 m s-1, respectively, which make them competitive energetic materials.

1,3-diaminoguanidine-2,4,5-trinitroimidazole salt and preparation method thereof

-

Paragraph 0019, (2017/07/20)

The invention discloses a 1,3-diaminoguanidine-2,4,5-trinitroimidazole salt and a preparation method thereof, belongs to the technical field of organic energetic materials and aims at solving the problem in the prior art that a TNT-based melt-cast explosive harms the environment in the use process. The method comprises the steps of using imidazole as a reaction raw material to generate 2,4,5-trinitroimidazole through step-by-step nitrification; enabling a nitrification product to react with a potassium carbonate/potassium chloride solution to form a salt to prepare 2,4,5-trinitroimidazole potassium salt; and finally obtaining a target product 1,3-diaminoguanidine-2,4,5-trinitroimidazole salt through double-decomposition reaction of 1,3-diamino guanidine hydrochloride and the 2,4,5-trinitroimidazole potassium salt. The preparation method is simple, low in preparation cost and good in security; and the final product 1,3-diaminoguanidine-2,4,5-trinitroimidazole salt is high in purity.

PROCESS FOR STRAIGHTENING KERATIN FIBRES WITH A HEATING MEANS AND DENATURING AGENTS

-

, (2010/03/02)

The invention relates to a process for straightening keratin fibres, comprising: (i) a step in which a straightening composition containing at least two denaturing agents is applied to the keratin fibres, (ii) a step in which the temperature of the keratin fibres is raised, using a heating means, to a temperature of between 110 and 250° C.

An Improved Synthesis of 3,6-Diamino-1,2,4,5-tetrazine. I

Coburn, Michael D.,Ott, Donald G.

, p. 1941 - 1945 (2007/10/02)

Treatment of 1,3-diaminoguanidine monohydrochloride (1) with 2,4-pentanedione (2) in alcohols under carefully controlled conditions gave 3,6-diamino-1,2-dihydro-1,2,4,5-tetrazine monohydrochloride (3) in 45-50percent yields along with 3,5-dimethyl-1H-pyrazole (4) and its hydrochloride 5.Oxidation of 3 with sodium perborate produced 3,6-diamino-1,2,4,5-tetrazine (6) in quantitative yield.

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