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142-46-1 Usage

Description

Hydrazodicarbothioamide is a white to off-white crystalline powder with a brown powder appearance. It is a chemical compound known for its various applications across different industries.

Uses

Used in Radiopharmaceutical Imaging:
Hydrazodicarbothioamide is used as a contrast agent in radiopharmaceutical imaging, enhancing the visualization of internal body structures and aiding in the diagnosis of various medical conditions.
Used in Enzyme Inhibition:
Hydrazodicarbothioamide serves as an inhibitor in the field of biochemistry, where it is employed to modulate enzyme function, providing valuable insights into enzyme mechanisms and potential therapeutic applications.
Used in Kidney Function Studies:
In the medical field, Hydrazodicarbothioamide is utilized in the study of kidney function, helping to assess and monitor renal health and diagnose kidney-related disorders.
Used in Treatment of Toxic Metal Poisoning:
Hydrazodicarbothioamide is used as an antidote for toxic metal poisoning, where it helps in mitigating the harmful effects of heavy metals on the body.
Used in Co-crystals Development:
In the pharmaceutical industry, Hydrazodicarbothioamide is used in the development of co-crystals, which are multi-component crystals that can improve the solubility, stability, and bioavailability of active pharmaceutical ingredients.
Used in Nonlinear Optics:
Hydrazodicarbothioamide is employed in the field of nonlinear optics, where it contributes to the generation of new coherent wavelengths, enhancing the performance of optical devices and systems.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Hydrazodicarbothioamide is related to dithiocarbamates. Flammable gases are generated by the combination of thiocarbamates and dithiocarbamates with aldehydes, nitrides, and hydrides. Thiocarbamates and dithiocarbamates are incompatible with acids, peroxides, and acid halides.

Fire Hazard

The flash point of Hydrazodicarbothioamide has not been determined, but Hydrazodicarbothioamide is probably combustible.

Check Digit Verification of cas no

The CAS Registry Mumber 142-46-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 142-46:
(5*1)+(4*4)+(3*2)+(2*4)+(1*6)=41
41 % 10 = 1
So 142-46-1 is a valid CAS Registry Number.
InChI:InChI=1/C2H6N4S2/c3-1(7)5-6-2(4)8/h(H3,3,5,7)(H3,4,6,8)

142-46-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (A16667)  2,5-Dithiobiurea, 97%   

  • 142-46-1

  • 25g

  • 379.0CNY

  • Detail
  • Alfa Aesar

  • (A16667)  2,5-Dithiobiurea, 97%   

  • 142-46-1

  • 100g

  • 729.0CNY

  • Detail

142-46-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Hydrazodicarbothioamide

1.2 Other means of identification

Product number -
Other names DITHIOUREA

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:142-46-1 SDS

142-46-1Synthetic route

1-benzylidene thiosemicarbazide
1627-73-2

1-benzylidene thiosemicarbazide

potassium ethoxide
917-58-8

potassium ethoxide

A

bithiourea
142-46-1

bithiourea

B

lophine
484-47-9

lophine

C

2,4,6-triphenyl-1,3,5-triazine
493-77-6

2,4,6-triphenyl-1,3,5-triazine

D

1-ethyl-2,4,5-triphenyl imidazole
7196-80-7

1-ethyl-2,4,5-triphenyl imidazole

E

benzoic acid
65-85-0

benzoic acid

Conditions
ConditionsYield
at 275℃; for 1h; Mechanism;A 65%
B 28%
C n/a
D n/a
E 23%
ammonium thiocyanate
1147550-11-5

ammonium thiocyanate

bithiourea
142-46-1

bithiourea

Conditions
ConditionsYield
With hydrazine hydrochloride In water at 120℃; for 15h; Addition;58%
With water; hydrazinium sulfate higher-melting form of hydrazine-N.N'-bis-carbothioic acid amide;
With hydrazinium sulfate
With hydrazine
With sulfuric acid; hydrazine hydrate
potassium thioacyanate
333-20-0

potassium thioacyanate

A

bithiourea
142-46-1

bithiourea

B

thiosemicarbazide
79-19-6

thiosemicarbazide

Conditions
ConditionsYield
With water; hydrazinium sulfate
thiosemicarbazide
79-19-6

thiosemicarbazide

bithiourea
142-46-1

bithiourea

Conditions
ConditionsYield
With hydrogenchloride; water
3,7-dimethyl-tetrahydro-[1,2,4]triazolo[1,2-a][1,2,4]triazole-1,5-dithione
16085-50-0

3,7-dimethyl-tetrahydro-[1,2,4]triazolo[1,2-a][1,2,4]triazole-1,5-dithione

water
7732-18-5

water

A

bithiourea
142-46-1

bithiourea

B

acetaldehyde
75-07-0

acetaldehyde

Conditions
ConditionsYield
Hydrolysis;
3,7-diethyl-3,7-dimethyl-tetrahydro-[1,2,4]triazolo[1,2-a][1,2,4]triazole-1,5-dithione
52578-79-7

3,7-diethyl-3,7-dimethyl-tetrahydro-[1,2,4]triazolo[1,2-a][1,2,4]triazole-1,5-dithione

water
7732-18-5

water

A

bithiourea
142-46-1

bithiourea

B

butanone
78-93-3

butanone

Conditions
ConditionsYield
beim Erhitzen <15h>;
higher-melting form of dithio hydrazodicarbamide

higher-melting form of dithio hydrazodicarbamide

bithiourea
142-46-1

bithiourea

Conditions
ConditionsYield
With hydrogenchloride lower-melting form of hydrazine-N.N'-bis-carbothioic acid amide;
With sodium hydroxide dann Faellen mit verd.HCl; lower-melting form of hydrazine-N.N'-bis-carbothioic acid amide;
ammonium thiocyanate
1147550-11-5

ammonium thiocyanate

hydrochloride of hydrazine

hydrochloride of hydrazine

bithiourea
142-46-1

bithiourea

Conditions
ConditionsYield
With water at 100℃; im geschlossenen Rohr;
thiocyanate of hydrazine

thiocyanate of hydrazine

bithiourea
142-46-1

bithiourea

Conditions
ConditionsYield
With water at 100℃; im geschlossenen Rohr;
ammonium thiocyanate
28241-61-4

ammonium thiocyanate

bithiourea
142-46-1

bithiourea

Conditions
ConditionsYield
With sulfuric acid; hydrazine hydrate In water at 100 - 103℃; for 3h;
semicarbazide hydrochloride
563-41-7

semicarbazide hydrochloride

potassium thioacyanate
333-20-0

potassium thioacyanate

bithiourea
142-46-1

bithiourea

Conditions
ConditionsYield
In water for 3h; Time; Reflux;
bithiourea
142-46-1

bithiourea

2,5-diamino-1,3,4-thiadiazole
2937-81-7

2,5-diamino-1,3,4-thiadiazole

Conditions
ConditionsYield
With dihydrogen peroxide In water98%
With dihydrogen peroxide In water at 50 - 60℃; for 1h;96.4%
With dihydrogen peroxide In water at 50℃; for 0.166667h;42%
bithiourea
142-46-1

bithiourea

2-bromo-7-methyl-5-oxo-5H-1,3,4-thiadiazolo<3,2-a>pyrimidine

2-bromo-7-methyl-5-oxo-5H-1,3,4-thiadiazolo<3,2-a>pyrimidine

C8H9N7S3O*HBr

C8H9N7S3O*HBr

Conditions
ConditionsYield
In ethanol for 2h; Heating;95%
bithiourea
142-46-1

bithiourea

methyl 3-phenyl-3-chloro-2-ketopropionate
32803-73-9

methyl 3-phenyl-3-chloro-2-ketopropionate

2-hydrazo-4-methoxycarbonyl-5-phenylthiazole dihydrochloride

2-hydrazo-4-methoxycarbonyl-5-phenylthiazole dihydrochloride

Conditions
ConditionsYield
In methanol for 3h; Hantzsch reaction; Heating;90%
bithiourea
142-46-1

bithiourea

1-chloroacetophenone
532-27-4

1-chloroacetophenone

4,4'-diphenyl-2,2'-diazane-1,2-diyl-bis-thiazole
76187-15-0

4,4'-diphenyl-2,2'-diazane-1,2-diyl-bis-thiazole

Conditions
ConditionsYield
In methanol at 30℃; for 12h; Condensation; cyclization;78%
With ethanol
bithiourea
142-46-1

bithiourea

1-chloroacetophenone
532-27-4

1-chloroacetophenone

4,4'-diphenyl-[5,5'-bithiazole]-2,2'-diamine
109249-88-9

4,4'-diphenyl-[5,5'-bithiazole]-2,2'-diamine

Conditions
ConditionsYield
In methanol at 75℃; for 13h; Condensation; rearrangement;78%
bithiourea
142-46-1

bithiourea

chloroacetone
78-95-5

chloroacetone

4,4'-dimethyl-[5,5']bithiazolyl-2,2'-diamine
94273-51-5

4,4'-dimethyl-[5,5']bithiazolyl-2,2'-diamine

Conditions
ConditionsYield
In water at 120℃; for 14h; Condensation; rearrangement;75%
bithiourea
142-46-1

bithiourea

1-bromo-5-hexyltridecan-2-one

1-bromo-5-hexyltridecan-2-one

1,2-bis(4-(3-hexylundecyl)thiazol-2-yl)diazene

1,2-bis(4-(3-hexylundecyl)thiazol-2-yl)diazene

Conditions
ConditionsYield
Stage #1: bithiourea; 1-bromo-5-hexyltridecan-2-one In ethanol at 50℃; for 2.5h; Inert atmosphere;
Stage #2: With sodium nitrite In water for 1h; Inert atmosphere;
75%
bithiourea
142-46-1

bithiourea

chloroacetone
78-95-5

chloroacetone

1,2-bis(4-methylthiazol-2-yl)hydrazine
287475-98-3

1,2-bis(4-methylthiazol-2-yl)hydrazine

Conditions
ConditionsYield
In methanol at 40℃; for 12h; Condensation; cyclization;74%
bithiourea
142-46-1

bithiourea

chloroacetaldehyde dimethyl acetal
97-97-2

chloroacetaldehyde dimethyl acetal

2,2'-diazane-1,2-diyl-bis-thiazole
120855-13-2

2,2'-diazane-1,2-diyl-bis-thiazole

Conditions
ConditionsYield
With hydrogenchloride In methanol at 55℃; for 15h; Condensation; cyclization;70%
3-bromoacetyl-1-ethylquinoxalin-2(1H)-one
879499-64-6

3-bromoacetyl-1-ethylquinoxalin-2(1H)-one

bithiourea
142-46-1

bithiourea

4,4'-bis(1-ethyl-2-oxo-1,2-dihydroquinoxalin-3-yl)-2,2'-azothiazole

4,4'-bis(1-ethyl-2-oxo-1,2-dihydroquinoxalin-3-yl)-2,2'-azothiazole

Conditions
ConditionsYield
Stage #1: 3-bromoacetyl-1-ethylquinoxalin-2(1H)-one; bithiourea In methanol for 1.5h; Heating;
Stage #2: With sodium hydrogencarbonate
Stage #3: In dimethyl sulfoxide at 100℃; for 1h;
63%
cadmium(II) chloride monohydrate

cadmium(II) chloride monohydrate

bithiourea
142-46-1

bithiourea

Cd(dithiobiurea)Cl2

Cd(dithiobiurea)Cl2

Conditions
ConditionsYield
In water aq. soln. of CdCl2*H2O added to hot soln. of dithiobiurea in water, suspn. heated on water bath for 30 min; suspn. cooled, ppt. filtered off, washed with water, dried at room temp.; elem. anal.;63%
3-bromoacetylquinoxalin-2(1H)-one
879499-63-5

3-bromoacetylquinoxalin-2(1H)-one

bithiourea
142-46-1

bithiourea

4,4'-bis(2-oxo-1,2-dihydroquinoxalin-3-yl)-2,2'-azothiazole

4,4'-bis(2-oxo-1,2-dihydroquinoxalin-3-yl)-2,2'-azothiazole

Conditions
ConditionsYield
Stage #1: 3-bromoacetylquinoxalin-2(1H)-one; bithiourea In methanol for 1.5h; Heating;
Stage #2: With sodium hydrogencarbonate
Stage #3: In dimethyl sulfoxide at 100℃; for 1h;
60%
bithiourea
142-46-1

bithiourea

chloroacetaldehyde dimethyl acetal
97-97-2

chloroacetaldehyde dimethyl acetal

2,2'-diamino-5,5'-bithiazole

2,2'-diamino-5,5'-bithiazole

Conditions
ConditionsYield
With hydrogenchloride In water at 130℃; for 16h; Condensation; rearrangement;58%
bithiourea
142-46-1

bithiourea

phenyl propargyl ketone
3623-15-2

phenyl propargyl ketone

4-[2-benzoylvinylsulfanyl(imino)methyl]-5-phenacyl-1,3,4-thiadiazolidin-2-iminium perchlorate

4-[2-benzoylvinylsulfanyl(imino)methyl]-5-phenacyl-1,3,4-thiadiazolidin-2-iminium perchlorate

Conditions
ConditionsYield
With perchloric acid In acetic acid at 20℃; for 8h;45%
With perchloric acid In acetic acid at 20℃; for 8h;33%
bithiourea
142-46-1

bithiourea

S,S'-dimethyl-dithiodiisobiurea
74586-16-6

S,S'-dimethyl-dithiodiisobiurea

Conditions
ConditionsYield
With diethyl ether
1,2-dichloroethyl acetate
10140-87-1

1,2-dichloroethyl acetate

bithiourea
142-46-1

bithiourea

2,2'-diazane-1,2-diyl-bis-thiazole
120855-13-2

2,2'-diazane-1,2-diyl-bis-thiazole

bithiourea
142-46-1

bithiourea

2-Bromopropionic acid
598-72-1

2-Bromopropionic acid

5,5'-dimethyl-2,2'-azino-bis-thiazolidin-4-one
62807-80-1

5,5'-dimethyl-2,2'-azino-bis-thiazolidin-4-one

Conditions
ConditionsYield
With water
2-Bromobutyric acid
80-58-0

2-Bromobutyric acid

bithiourea
142-46-1

bithiourea

5,5'-diethyl-2,2'-azino-bis-thiazolidin-4-one
114166-04-0

5,5'-diethyl-2,2'-azino-bis-thiazolidin-4-one

bithiourea
142-46-1

bithiourea

1,2-dichloro-2-ethoxyethane
623-46-1

1,2-dichloro-2-ethoxyethane

2,2'-diazane-1,2-diyl-bis-thiazole
120855-13-2

2,2'-diazane-1,2-diyl-bis-thiazole

bithiourea
142-46-1

bithiourea

bromo-2 propanal
19967-57-8

bromo-2 propanal

bis-(5-methyl-thiazol-2-yl)-diazene

bis-(5-methyl-thiazol-2-yl)-diazene

Conditions
ConditionsYield
With ethanol anschliessend Erwaermen mit FeCl3 in wss. HCl;
bithiourea
142-46-1

bithiourea

2-bromo-3-methyl-butyraldehyde
64932-36-1

2-bromo-3-methyl-butyraldehyde

N,N'-bis-(5-isopropyl-thiazol-2-yl)-hydrazine

N,N'-bis-(5-isopropyl-thiazol-2-yl)-hydrazine

Conditions
ConditionsYield
With ethanol
bithiourea
142-46-1

bithiourea

ethyl Bromopyruvate
70-23-5

ethyl Bromopyruvate

diethyl 2,2'-(hydrazine-1,2-diyl)bis(thiazole-4-carboxylate)

diethyl 2,2'-(hydrazine-1,2-diyl)bis(thiazole-4-carboxylate)

Conditions
ConditionsYield
With ethanol
In ethanol for 2h; Inert atmosphere; Reflux;
bithiourea
142-46-1

bithiourea

ethyl 3-bromo-4-oxopentanoate
54260-84-3

ethyl 3-bromo-4-oxopentanoate

N,N'-bis-(5-ethoxycarbonylmethyl-4-methyl-thiazol-2-yl)-hydrazine; dihydrobromide

N,N'-bis-(5-ethoxycarbonylmethyl-4-methyl-thiazol-2-yl)-hydrazine; dihydrobromide

Conditions
ConditionsYield
With ethanol
bithiourea
142-46-1

bithiourea

diethyl 2-chloro-3-oxopentanedioate
476415-70-0

diethyl 2-chloro-3-oxopentanedioate

4,4'-bis-ethoxycarbonylmethyl-2,2'-hydrazo-bis-thiazole-5-carboxylic acid diethyl ester

4,4'-bis-ethoxycarbonylmethyl-2,2'-hydrazo-bis-thiazole-5-carboxylic acid diethyl ester

Conditions
ConditionsYield
With ethanol
bithiourea
142-46-1

bithiourea

ethyl 2-chloro-3-oxo-3-phenylpropionate
41381-97-9, 146368-56-1

ethyl 2-chloro-3-oxo-3-phenylpropionate

4,4'-diphenyl-2,2'-hydrazo-bis-thiazole-5-carboxylic acid diethyl ester

4,4'-diphenyl-2,2'-hydrazo-bis-thiazole-5-carboxylic acid diethyl ester

Conditions
ConditionsYield
With ethanol
bithiourea
142-46-1

bithiourea

5-amino-2,3-dihydro-1H-1,2,4-triazole-3-thione
16691-43-3

5-amino-2,3-dihydro-1H-1,2,4-triazole-3-thione

Conditions
ConditionsYield
With alkaline solution
at 215℃;
bithiourea
142-46-1

bithiourea

5-thioxo-[1,2,4]triazolidin-3-one hydrazone
3310-81-4

5-thioxo-[1,2,4]triazolidin-3-one hydrazone

Conditions
ConditionsYield
With water; hydrazine
With ethanol; hydrazine hydrate
bithiourea
142-46-1

bithiourea

4,5-diamino-2,4-dihydro-[1,2,4]triazole-3-thione
3529-50-8

4,5-diamino-2,4-dihydro-[1,2,4]triazole-3-thione

Conditions
ConditionsYield
With water; hydrazine hydrate
With ethanol; hydrazine hydrate
With hydrazine

142-46-1Relevant articles and documents

Facile synthesis of novel bis-derivatives of 2,5-diamino-thiadiazole/N,N′-thiocarbohydrazide and their biological perspective

Bhatt, Priyanka,Sreekanth,Jha, Anjali

, p. 7241 - 7258 (2018)

A series of new bis derivatives of 2,5-thiadiazole and N,N′-thiocarbohydrazide along with their transition metal complexes were synthesized by green methods (sonochemical and microwave), i.e., energy and time efficient and operationally more simple than existing conventional methods. All the synthesized compounds were fully characterized by routine analytical techniques and subjected to a preliminary biological screening. These novel characterized compounds were screened for antimicrobial activities and showed promising results. A few potent compounds were also tested for antitumor activities against MDA-MB231 (human breast carcinoma cell line) and compound 5 has emerged as a potential antitumor compound followed by compound 2, 10 and 9, with IC50 values of 29.48, 32.25, 32.34 and 34.34?μg/ml, respectively. To understand the binding interactions of these compounds, in silico studies were performed using the AUTODOCK 4.2 suite and found to be supportive of the experimental results.

Synthesis and antifungal evaluation of 1,2,4-triazolo[1,5-α] pyrimidine bearing 1,2,4-triazole heterocycle derivatives

Chen,Xiang,Fu,Zeng,Zhu

scheme or table, p. 602 - 608 (2012/01/02)

In order to search novel fungicides with higher activity, 28 new 1,2,4-triazolo[1,5-α]pyrimidine derivatives bearing 1,2,4-triazole heterocycle were synthesized. Their structures were characterized by 1H NMR spectroscopy, mass spectrometry and elemental analyses. With triadimefon, validamycin and carbendazim as positive controls, the antifungal activities of 28 compounds against Fusarium oxysporum f. sp. vasinfectum, Gibberella sanbinetti, Cercospora beticola Sacc., Physaclospora piricola and Rhizoctonia solani were evaluated. Compound 2-[(5-(2,6- difluorobenzylthio)-4- phenyl-4H-1,2,4-triazol-3-yl)methylthio]-5,7-dimethyl[1,2,4]triazolo[1, 5-α]pyrimidine (19) showed potent antifungal activities against G. sanbinetti, C. beticola, P. piricola and R. solani. On the basis of the biological results, structure-activity relationships of these compounds were also discussed.

PRODUCTS FROM REACTION OF BENZALDEHYDE THIOSEMICARBAZONE WITH POTASSIUM ETHOXIDE

Marshalkin, M. F.,Yakhontov, L. N.

, p. 2273 - 2276 (2007/10/02)

When heated with potassium ethoxide, benzaldehyde thiosemicarbazone gives a mixture of 2,4,5-triphenylimidazole, hydrazodithioformamide, benzoic acid, and benzaldehyde oxime.It was shown that these compounds are formed through the intermediate benzaldehyde azine and benzonitrile.

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