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Amidinothiourea - 98%, high purity , CAS No.2114-02-5

    Grade & Purity:
  • ≥98%
In stock
Item Number
A111256
Grouped product items
SKU Size
Availability
Price Qty
A111256-5g
5g
4
$9.90
A111256-25g
25g
3
$30.90
A111256-100g
100g
4
$82.90
A111256-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$216.90

Basic Description

Synonyms 2-Imino-4-thiobiuret, 99% | Amidinothiourea | EN300-34314 | guanyl isothiourea | (diaminomethylidene)thiourea | 1-(diaminomethylene)thiourea | EINECS 218-308-0 | E75731 | BBL008942 | diaminomethylidenethiourea | N-Amidinothiourea | N-amidino-thiourea | 1-
Specifications & Purity ≥98%
Shipped In Normal
Product Description

Application

2-Imino-4-thiobiuret is used in the design and synthesis of guanylthiourea derivatives which are potential inhibitors of plasmodium falciparum dihydrofolate reductase enzyme. 2-Imino-4-thiobiuret is also used as a reagent in recyclization reactions of N-arylmaleimides with polynucleophilic compounds.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic nitrogen compounds
Class Organonitrogen compounds
Subclass Guanidines
Intermediate Tree Nodes Not available
Direct Parent Guanidines
Alternative Parents Propargyl-type 1,3-dipolar organic compounds  Carboximidamides  Organosulfur compounds  Organopnictogen compounds  Imines  Hydrocarbon derivatives  
Molecular Framework Aliphatic acyclic compounds
Substituents Guanidine - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organopnictogen compound - Hydrocarbon derivative - Organosulfur compound - Imine - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as guanidines. These are compounds containing a guanidine moiety, with the general structure (R1R2N)(R3R4N)C=N-R5.
External Descriptors Not available

Names and Identifiers

Pubchem Sid 488192282
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488192282
IUPAC Name diaminomethylidenethiourea
INCHI InChI=1S/C2H6N4S/c3-1(4)6-2(5)7/h(H6,3,4,5,6,7)
InChIKey OKGXJRGLYVRVNE-UHFFFAOYSA-N
Smiles C(=NC(=S)N)(N)N
Isomeric SMILES C(=NC(=S)N)(N)N
WGK Germany 3
RTECS YR8250000
Molecular Weight 118.16
Reaxy-Rn 3587727
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3587727&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

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.

11 results found

Lot Number Certificate Type Date Item
F2103076 Certificate of Analysis Mar 04, 2025 A111256
H1704011 Certificate of Analysis Mar 04, 2025 A111256
A2513231 Certificate of Analysis Jun 20, 2024 A111256
A2513237 Certificate of Analysis Jun 20, 2024 A111256
G1818008 Certificate of Analysis May 07, 2022 A111256
E2311061 Certificate of Analysis Dec 13, 2021 A111256
B2313017 Certificate of Analysis Dec 13, 2021 A111256
A2425080 Certificate of Analysis Dec 13, 2021 A111256
D2401046 Certificate of Analysis Dec 13, 2021 A111256
B2313018 Certificate of Analysis Dec 13, 2021 A111256
B2313019 Certificate of Analysis Dec 13, 2021 A111256

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Chemical and Physical Properties

Solubility Soluble in water (70g/L).
Melt Point(°C) 160-164°C
Molecular Weight 118.160 g/mol
XLogP3 -1.300
Hydrogen Bond Donor Count 3
Hydrogen Bond Acceptor Count 1
Rotatable Bond Count 0
Exact Mass 118.031 Da
Monoisotopic Mass 118.031 Da
Topological Polar Surface Area 123.000 Ų
Heavy Atom Count 7
Formal Charge 0
Complexity 102.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Lulu Zhang, Long Jiang, Yaojie Liu, Zongjiang Yu, Ximin Chen, Xiaomeng Su, Mo Xian, Weizhi Sun, Chao Xu.  (2023)  The design and adsorption behaviors study of Pd(II) removal materials deriving from quantitative electron transfer ratio evaluation.  Journal of Environmental Chemical Engineering,  11  (110264). 
2. Zhu Lingkai, Xi Man, Yao Yuyuan, Lan Ping.  (2023)  Thiol -functionalized activated carbon fibers as efficient adsorbents for Pb2+.  MATERIALS CHEMISTRY AND PHYSICS,  302  (127552). 
3. Xiao Xudong, Lin Siying, Zhang Liping, Meng Huiyuan, Zhou Jing, Li Qi, Liu Jianan, Qiao Panzhe, Jiang Baojiang, Fu Honggang.  (2022)  Constructing Pd-N interactions in Pd/g-C3N4 to improve the charge dynamics for efficient photocatalytic hydrogen evolution.  Nano Research,  15  (4): (2928-2934). 
4. Heping Wang, Bang Feng, Qianwen Zhang, Qiang Du, Qiuhong Bai, Cong Li, Yehua Shen.  (2021)  Amidinothiourea-linked covalent organic framework for the adsorption of heavy metal ions.  POLYMER INTERNATIONAL,  71  (1): (38-46). 
5. Fangxiang Song, Xianquan Ao, Qianlin Chen.  (2022)  Effect of heteroatom doping on the charge storage and operating voltage window of nickel-based sulfide composite electrodes in alkaline electrolytes.  CHEMICAL ENGINEERING JOURNAL,  427  (130885). 
6. Chaokun Yang, Yanglin Chen, Ping Xu, Li Yang, Jiaxu Zhang, Jianmin Sun.  (2020)  Facile synthesis of zinc halide-based ionic liquid for efficient conversion of carbon dioxide to cyclic carbonates.  Molecular Catalysis,  480  (110637). 
7. Huicai Wang, Zhenwen Wang, Ruirui Yue, Feng Gao, Ruili Ren, Junfu Wei, Xiaolei Wang, Zhiyun Kong.  (2020)  Functional group-rich hyperbranched magnetic material for simultaneous efficient removal of heavy metal ions from aqueous solution.  JOURNAL OF HAZARDOUS MATERIALS,  384  (121288). 
8. Lei Guo, Lei Zhu, Savaş Kaya, Rui Sun, Alessandra Gilda Ritacca, Kai Wang, Jun Chang.  (2024)  Electrochemical and surface investigations of N, S codoped carbon dots as effective corrosion inhibitor for mild steel in acidic solution.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,  702  (135062). 

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