Thiourea - Premium-Grade Reagents, ≥99% , CAS No.62-56-6

CAS: 62-56-6 Cat. No.: T112512 Formule: CH4N2S Poids moléculaire: 76.12 Beilstein Registry Number: 605327 Numéro CE: 200-543-5 PubChem CID: 2723790
DISPONIBLE À COMMANDE
QUALITÉ & PURETÉ Premium-Grade Reagents ? Premium-grade reagents with enhanced purity and tighter QC than standard grades. Use for demanding applications needing extra consistency. ≥99%
Synonyms
2-Thiopseudourea | 2-Thio-Pseudourea | CHEBI:36946 | NCGC00259422-01 | Thiomocovina | THIOUREA [INCI] | NSC 5033 | thiopseudourea | T0445 | aminothioamide | NCGC00091199-01 | Thiokarbamid | UN 2877 | BCP27948 | GYV9AM2QAG | Sulfouren | S C (N H2)2 | (NH2)
Storage
Room temperature,Argon charged
Shipped In
FedEx DG Service
★
Taille
Allemagne (EU)
USA*
Prix
Qté
25g
T112512-25g
—
5 En stock
8,59€
100g
T112512-100g
—
2 En stock
10,33€
500g
T112512-500g
1 En stock
En stock ≥10
20,74€
Enter a quantity for the sizes you want to add.
🧪
Pourquoi cette qualité

Premium-Grade Reagents, ≥99% Premium-Grade Reagents pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.

🌡

Stockage & expédition

Room temperature,Argon charged Expédition FedEx DG Service. Consultez le COA spécifique au lot pour les spécifications exactes.

📋

Documents qualité

SDS, COA, fiche technique et fiche de spécifications disponibles au téléchargement. COA spécifique au lot accessible via la recherche par numéro de lot.

📚

Preuve documentaire

Cité dans 1759 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Spécifications

Synonymes
2-Thiopseudourea | 2-Thio-Pseudourea | CHEBI:36946 | NCGC00259422-01 | Thiomocovina | THIOUREA [INCI] | NSC 5033 | thiopseudourea | T0445 | aminothioamide | NCGC00091199-01 | Thiokarbamid | UN 2877 | BCP27948 | GYV9AM2QAG | Sulfouren | S C (N H2)2 | (NH2)
Spécifications et pureté
Premium-Grade Reagents, ≥99%
Mécanismes biochimiques et physiologiques
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
Conditions de stockage de stockage
Room temperature,Argon charged
Expédié en
FedEx DG Service
Grade
Premium-Grade Reagents
Pureté
≥99%
Noms et identifiants
Pubchem Sid
Sourires canoniques
C(=S)(N)N
IUPAC Name
thiourea
InChIKey
UMGDCJDMYOKAJW-UHFFFAOYSA-N
INCHI
1S/CH4N2S/c2-1(3)4/h(H4,2,3,4)
Isomères SMILES
C(=S)(N)N
WGK Allemagne
2
RTECS
YU2800000
PubChem CID
2723790
Numéro ONU
2811
Groupe d'emballage
I
Poids moléculaire
76.12
Beilstein
605327

Documentation

📋 Fiche de données de sécurité (FDS)

Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.

<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3

✅ Certificat d'analyse (COA)

Données qualité spécifiques au lot. Saisissez votre numéro de lot pour récupérer le COA exact.

Rechercher le COA →

📊 Fiche technique

Résumé de référence rapide des spécifications et applications du produit.

Voir la fiche technique →

🔬 Fiche de spécifications

Attributs de qualité complets et critères d'acceptation pour cette qualité.

Voir la fiche de spécifications →

Données avancées

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganosulfur compounds
ClasseThioureas
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
DescriptionThis 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
Structure 3D
Modèle de structure chimique interactif





Cibles associées (humaines)
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
Cibles associées (non humaines)
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
Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
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.

44 results found

Lot NumberCertificate TypeDateArticle
I2607717I2607717Certificate of AnalysisJul 09, 2026 T112512
I2607801I2607801Certificate of AnalysisJul 09, 2026 T112512
I2607800I2607800Certificate of AnalysisJul 09, 2026 T112512
I2607799I2607799Certificate of AnalysisJul 09, 2026 T112512
A2622462A2622462Certificate of AnalysisJan 09, 2026 T112512
A2622461A2622461Certificate of AnalysisJan 09, 2026 T112512
G2617129G2617129Certificate of AnalysisJan 09, 2026 T112512
A2622515A2622515Certificate of AnalysisJan 09, 2026 T112512
A2622514A2622514Certificate of AnalysisJan 09, 2026 T112512
I2518430I2518430Certificate of AnalysisJun 24, 2025 T112512
I2525470I2525470Certificate of AnalysisJun 24, 2025 T112512
I2525469I2525469Certificate of AnalysisJun 24, 2025 T112512
I2525468I2525468Certificate of AnalysisJun 24, 2025 T112512
I2525433I2525433Certificate of AnalysisJun 24, 2025 T112512
H2529570H2529570Certificate of AnalysisJun 24, 2025 T112512
H2529569H2529569Certificate of AnalysisJun 24, 2025 T112512
H2529389H2529389Certificate of AnalysisJun 24, 2025 T112512
G2515109G2515109Certificate of AnalysisFeb 26, 2025 T112512
C2510319C2510319Certificate of AnalysisFeb 26, 2025 T112512
C2510320C2510320Certificate of AnalysisFeb 26, 2025 T112512
C2510321C2510321Certificate of AnalysisFeb 26, 2025 T112512
C2510318C2510318Certificate of AnalysisFeb 26, 2025 T112512
K2419569K2419569Certificate of AnalysisNov 01, 2024 T112512
K2419565K2419565Certificate of AnalysisNov 01, 2024 T112512
K2419567K2419567Certificate of AnalysisNov 01, 2024 T112512
K2419568K2419568Certificate of AnalysisNov 01, 2024 T112512
D2418505D2418505Certificate of AnalysisApr 02, 2024 T112512
D2418352D2418352Certificate of AnalysisApr 02, 2024 T112512
D2418345D2418345Certificate of AnalysisApr 02, 2024 T112512
D2418344D2418344Certificate of AnalysisApr 02, 2024 T112512
K2313591K2313591Certificate of AnalysisOct 24, 2023 T112512
K2313581K2313581Certificate of AnalysisOct 24, 2023 T112512
K2313508K2313508Certificate of AnalysisOct 24, 2023 T112512
K2313432K2313432Certificate of AnalysisOct 24, 2023 T112512
E2325910E2325910Certificate of AnalysisMay 09, 2023 T112512
E2325888E2325888Certificate of AnalysisMay 09, 2023 T112512
E2325901E2325901Certificate of AnalysisMay 09, 2023 T112512
E2325913E2325913Certificate of AnalysisMay 09, 2023 T112512
E2325912E2325912Certificate of AnalysisMay 09, 2023 T112512
E2325908E2325908Certificate of AnalysisMay 09, 2023 T112512
D2225002D2225002Certificate of AnalysisMar 12, 2022 T112512
D2225004D2225004Certificate of AnalysisMar 12, 2022 T112512
D2225006D2225006Certificate of AnalysisMar 12, 2022 T112512
D2225007D2225007Certificate of AnalysisMar 12, 2022 T112512
Propriétés chimiques et physiques
SolubilitéSoluble in water; Degree of Solubility in water: 142 g/l 25 °C; Soluble in Alcohol; Very slightly soluble in Ether
SensibilitéAir Sensitive
Point de fusion (°C)182°C
Poids moléculaire76.120 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
FAQ et articles
Premium-Grade Reagents
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
Calculateurs de solution
Avis

Avis des clients

Souhaitez-vous que nous vous envoyions un message lorsque des réductions seront disponibles?

Me rappeler plus tard

Merci ! Veuillez vérifier votre boîte de réception e-mail pour confirmer.

Oups ! Les notifications sont désactivées.