Thiourea - ACS, ≥99% , CAS No.62-56-6

CAS: 62-56-6 Cat. No.: T112514 Fórmula: CH4N2S Peso molecular: 76.12 Beilstein Registry Number: 605327 Número EC: 200-543-5 PubChem CID: 2723790
Disponible para pedir
GRADE & PURITY ACS ? ACS grade — meets American Chemical Society specifications, the analytical benchmark in the US. Use for analytical and QC work needing ACS-defined purity. ≥99%
Synonyms
2-Thiourea | Thiocarbamide | Isothiourea
Storage
Room temperature,Argon charged
Shipped In
FedEx DG Service
★
Size
Alemania (EU)
USA*
Price
Qty
500g
T112514-500g
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2 Disponible

51,98€

78,01€
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T112514-12×500g
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Why this grade

ACS, ≥99% ACS for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Argon charged Ships FedEx DG Service Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 1738 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Application:

Chaotropic agent; strong denaturant. Increases solubility and recovery of proteins
Thiourea has been used:
as a component of lysis buffer for liver tissue homogenization
in 2-D sample buffer for two-dimensional in-gel protein tyrosine phosphatases (PTP) assay
in rehydration buffer for protein extraction

Specifications

Sinónimos
2-Thiourea | Thiocarbamide | Isothiourea
Especificaciones y pureza
ACS, ≥99%
Mecanismos bioquímicos y fisiológicos
Thiourea is a free radical scavenger of the peroxide radical. It was shown to inhibit lipid peroxidation and ultraviolet (UV)-induced crosslinking of collagen. Bud dormancy in plants can be inhibited by thiourea which is used as a growth stimulator. It is
Condiciones de almacenamiento de almacenamiento
Room temperature,Argon charged
Enviado en
FedEx DG Service
Grado
ACS
Pureza
≥99%
Nombres e identificadores
Pubchem Sid508815331
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/508815331
Sonrisas canónicasC(=S)(N)N
IUPAC Namethiourea
InChIKeyUMGDCJDMYOKAJW-UHFFFAOYSA-N
INCHI1S/CH4N2S/c2-1(3)4/h(H4,2,3,4)
Isómeros SMILES C(=S)(N)N
WGK Alemania 2
RTECS YU2800000
PubChem CID 2723790
Número ONU 2811
Grupo de embalaje I
Peso molecular 76.12
Beilstein 605327

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganosulfur compounds
ClaseThioureas
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentThioureas
Alternative Parents Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Thiourea - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as thioureas. These are organic compounds containing the thiourea functional group, a derivative of urea with the general structure (R1(N)R2C(=S)(R3)R4, R1-R4=H, alkyl, aryl), obtained by replacing the carbonyl group of urea with a thiocarbonyl group.
External Descriptors one-carbon compound - ureas - thioureas
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ATM Tchem Serine-protein kinase ATM (4198 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ATR Tchem Serine-protein kinase ATR (986 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
IDH1 Tclin Isocitrate dehydrogenase [NADP] cytoplasmic (40980 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADH1A Tclin Alcohol dehydrogenase (35 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Poliovirus 1 (1274 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Urease (750 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ureB Urease subunit alpha/Urease subunit beta (701 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

17 results found

Lot NumberCertificate TypeFechaArticulo
F2612335Certificate of AnalysisJun 01, 2026 T112514
L2522571Certificate of AnalysisDec 11, 2025 T112514
C2609457Certificate of AnalysisDec 11, 2025 T112514
H2505590Certificate of AnalysisJun 18, 2025 T112514
D2509521Certificate of AnalysisMar 12, 2025 T112514
L2423299Certificate of AnalysisDec 11, 2024 T112514
J2417799Certificate of AnalysisOct 10, 2024 T112514
D2417553Certificate of AnalysisApr 02, 2024 T112514
A2418336Certificate of AnalysisJan 09, 2024 T112514
B2520376Certificate of AnalysisJan 09, 2024 T112514
L2315220Certificate of AnalysisNov 30, 2023 T112514
I2319307Certificate of AnalysisAug 31, 2023 T112514
D2328245Certificate of AnalysisApr 18, 2023 T112514
C23241043Certificate of AnalysisNov 28, 2022 T112514
L2220444Certificate of AnalysisNov 28, 2022 T112514
J2209485Certificate of AnalysisMay 09, 2022 T112514
B2208211Certificate of AnalysisJan 08, 2022 T112514
Propiedades químicas y físicas
SolubilidadSoluble in water.
SensibilidadMoisture sensitive.
Punto de fusión (°C)182°C
Peso molecular76.120 g/mol
XLogP3-0.800
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass76.0095 Da
Monoisotopic Mass76.0095 Da
Topological Polar Surface Area84.100 Ų
Heavy Atom Count4
Formal Charge0
Complexity29.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Biginelli Reaction
How to Choose a Hydrogen Evolution (HER) Catalyst: Kinetic Barriers in Water Electrolysis, AWE/PEM/AEM Pathways, and a Materials-Family Roadmap (with a Product Map)
Plant Omics Panorama: Workflow Frameworks and Multi-Omics Integration from Genomics to Transcriptomics, Proteomics, and Metabolomics
Review of Chymotrypsin: Enzymological Properties, Catalytic Mechanism, and Research Applications
How to Select Thickeners for Strongly Acidic Cleaning Systems: Comparison of Thickening Mechanisms and Application Considerations for Fatty Amine Ethoxylates
Route Selection for Thiol Synthesis: C–S Bond Construction, Sulfur Source Forms, and Thiol Release
Direct Construction of Methylsulfonyl-Containing Heterocycles: Synthesis and Applications of Prefunctionalized Three-Carbon Vinamidinium Salts
Citations of This Product
Calculadoras de soluciones
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