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Thiosemicarbazide

CAS No.
79-19-6
Chemical Name:
Thiosemicarbazide
Synonyms
HYDRAZINECARBOTHIOAMIDE;TSC;Aminothiourea;n-aminothiourea;TSZ;3-thiosemicarbazide;CHP3;NSC 2213;ai3-16319;NSC 31792
CBNumber:
CB0132714
Molecular Formula:
CH5N3S
Molecular Weight:
91.14
MDL Number:
MFCD00007620
MOL File:
79-19-6.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-08-29 16:11:11

Thiosemicarbazide Properties

Melting point 180-183 °C (dec.)(lit.)
Boiling point 208.6±23.0 °C(Predicted)
Density 1.221 (estimate)
bulk density 500-600kg/m3
vapor pressure 1.15Pa at 25℃
refractive index 1.5800 (estimate)
storage temp. Store at +15°C to +25°C.
solubility DMSO : 125 mg/mL (1371.52 mM; Need ultrasonic)
pka pK1:1.5(+1) (25°C,μ=0.1)
form Powder
color White to light yellow
PH 5-7 (50g/l, H2O, 20℃)
biological source rabbit
Water Solubility soluble
Merck 14,9361
BRN 506320
Henry's Law Constant 1.5×104 mol/(m3Pa) at 25℃, HSDB (2015)
Stability Stable. Incompatible with strong oxidizing agents.
InChI 1S/CH5N3S/c2-1(5)4-3/h3H2,(H3,2,4,5)
InChIKey BRWIZMBXBAOCCF-UHFFFAOYSA-N
SMILES NNC(N)=S
LogP -1.67
CAS DataBase Reference 79-19-6(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 6056O8W6ET
NIST Chemistry Reference Hydrazinecarbothioamide(79-19-6)
EPA Substance Registry System Thiosemicarbazide (79-19-6)
UNSPSC Code 12352203
NACRES NA.41

SAFETY

Risk and Safety Statements

Symbol(GHS)  Skull and Crossbones (GHS06)
GHS06
Signal word  Danger
Hazard statements  H300-H412
Precautionary statements  P264-P270-P273-P301+P310-P405-P501
PPE Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  T+
Risk Statements  28-52/53-26/27/28
Safety Statements  22-26-36/37-45-61-28A-36/37/39
RIDADR  UN 2811 6.1/PG 2
WGK Germany  3
RTECS  VT4200000
8-9-23
TSCA  TSCA listed
HazardClass  6.1
PackingGroup  II
HS Code  29309070
HS Code  29335995
Storage Class 6.1A - Combustible acute toxic Cat. 1 and 2
very toxic hazardous materials
Hazard Classifications Acute Tox. 2 Oral
Aquatic Chronic 3
Hazardous Substances Data 79-19-6(Hazardous Substances Data)
Toxicity LD50 orally in adult Norway rats: 13 mg/kg, Dieke, Proc. Soc. Exp. Biol. Med. 70, 688 (1949)
REACH Registrations Active
Limited Quantities 0.5 Kg (solid)
Excepted Quantities Max Inner Pack (1g or 1ml) and Max Outer Pack (500g or 500ml)
NFPA 704
1
4 0

Thiosemicarbazide price More Price(48)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 89050 Thiosemicarbazide puriss. p.a., 98% 79-19-6 25g $53.5 2026-04-30 Buy
Sigma-Aldrich 89050 Thiosemicarbazide puriss. p.a., 98% 79-19-6 100g $71.6 2026-04-30 Buy
Sigma-Aldrich SAB1301171 ANTI-TESC (C-TERM) antibody produced in rabbit IgG fraction of antiserum, buffered aqueous solution 400 μL $496 2025-07-31 Buy
Sigma-Aldrich 8.21119 Thiosemicarbazide for synthesis 79-19-6 1kg $252 2022-05-15 Buy
TCI Chemical T0221 Thiosemicarbazide >98.0%(T) 79-19-6 25g $56 2026-04-30 Buy
Product number Packaging Price Buy
89050 25g $53.5 Buy
89050 100g $71.6 Buy
SAB1301171 400 μL $496 Buy
8.21119 1kg $252 Buy
T0221 25g $56 Buy

Thiosemicarbazide Chemical Properties, Uses, Production

Chemical Properties

Thiosemicarbazide is an odorless, white crystalline powder. It is soluble in water and ethanol; its solubility in cold water is 1%–2%, and in warm water is approximately 10%. Needle-like crystals can be obtained from aqueous solutions. It readily reacts with aldehydes and ketones to form specific crystalline products; it also readily reacts with carboxylic acids.

Uses

Used in TLC to stain alpha-keto acidsThiosemicarbazide is used as a reagent for ketones as well as chemical intermediate. It is involved in the detection of metals. It is also used in photography. Further, it is effective for controlling bacterial leaf blight in rice. In addition to this, it is used to prepare 1,3,4-thiadiazoles.

Uses

As a reagent for detection of metals.

Preparation

Thiosemicarbazide is produced from hydrazine hydrate and ammonium thiocyanate as raw materials, with acetaldehyde used as a catalyst. The chemical equations are as follows:
2H₂NNH₂·H₂O + H₂SO₄ → (H₂NNH₂)₂·H₂SO₄ + 2H₂O
(H₂NNH₂)₂·H₂SO₄ + 2NH₄SCN → 2H₂NNH₂·HSCN + (NH₄)₂SO₄

Definition

ChEBI: Hydrazinecarbothioamide is a member of the class of thioureas that is thiourea in which a hydrogen of one of the amino groups is replaced by an amino group. It is a member of hydrazines, a thiocarboxamide and a member of thioureas.

General Description

N-Aminothiourea is a white crystalline powder and is odorless. N-Aminothiourea is used as a reagent for ketones and certain metals, for photography and as a rodenticide. N-Aminothiourea is also effective for control of bacterial leaf blight of rice. Not a registered pesticide in the U.S. N-Aminothiourea is a chemical intermediate for herbicides and a reagent for detection of metals.

Reactivity Profile

Isocyanates and thioisocyanates are incompatible with many classes of compounds, reacting exothermically to release toxic gases. Reactions with amines, aldehydes, alcohols, alkali metals, ketones, mercaptans, strong oxidizers, hydrides, phenols, and peroxides can cause vigorous releases of heat. Acids and bases initiate polymerization reactions in these materials. Some isocyanates react with water to form amines and liberate carbon dioxide. Base-catalysed reactions of isocyanates with alcohols should be carried out in inert solvents. Such reactions in the absence of solvents often occur with explosive violence, [Wischmeyer(1969)].

Health Hazard

N-Aminothiourea is highly toxic by ingestion. May induce goiter and cause delayed toxic effects in blood and skin. May be mutagenic in human cells.

Fire Hazard

When heated to decomposition, very toxic fumes of sulfur oxides and nitrogen oxides are emitted.

Flammability and Explosibility

Non flammable

Safety Profile

Poison by ingestion, intraperitoneal, and intravenous routes. Questionable carcinogen with experimental tumorigenic data. Human mutation data reported. When heated to decomposition it emits very toxic fumes of NOx and SOx.

Potential Exposure

Thiosemicarbazide is a dithiocarbamide compound is used as an intermedialte for pharmaceuticals and herbicides; as a reagent for ketones and certain metals; in certain photography and dye operations; as a rodenticide. It is also effective for control of bacterial leaf blight of rice.

Shipping

UN2771 Thiosemicarbazide, pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials. UN2811 Toxic solids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required.

Purification Methods

Crystallise thiosemicarbazide from H2O (solubility is 20.3% w/w at 80o). The hydrochloride has m 190-191o(dec, 184o also reported). It forms salts with heavy metals. [Beilstein 3 H 195, 3 I 79, 3 II 134, 3 III 315, 3 IV 374.]

Incompatibilities

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.) and strong reducing agents; contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. May react with nitrates.

References

[1] Kurihara, H., et al. “Synthesis of Cyanohydrazine Derivatives from Thiosemicarbazide. Alkylating Reaction of Thiosemicarbazide Using Phase-Transfer Catalyst.” Nippon Kagaku Kaishi, 83 1, 1997, pp. 412–18, https://doi.org/10.1246/NIKKASHI.1997.412.
[2] Varvaresou, Athanasia, et al. “ChemInform Abstract: Synthesis and Biological Evaluation of Indole Containing Derivatives of Thiosemicarbazide and Their Cyclic 1,2,4-Triazole and 1,3,4-Thiadiazole Analogues.” ChemInform, 31 15, 2010, https://doi.org/10.1002/chin.200015117.

Global Suppliers ( 595)
Supplier Tel Email Country ProdList Advantage
Hubei zhonglong Kangsheng Fine Chemical Co., Ltd 027-027-83850178 18162590268 1984393783@qq.com China 4740 58
Hubei Hicks Biochemical Co., Ltd 17362916295; 17362916295 w17362916295@163.com China 3985 58
Huai Hua Binfengchem Co., Ltd 0745-2866851 17711757908 3907837691@qq.com China 4744 58
Jinan Shengqi Pharmaceutical Co., Ltd 0531-82687819 15610111696 xgc01@orgachem.com China 176 58
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J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
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Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
3B Pharmachem (Wuhan) International Co.,Ltd. 18930552037 3bsc@sina.com China 15813 69

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