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96-45-7

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96-45-7 Usage

Description

Ethylenethiourea, a thiourea derivative, is a rubber chemical. It has caused contact dermatitis mainly in rubber workers.

Chemical Properties

Ethylene thiourea is a white to light green, needle-like crystalline solid with a faint amine odor. It is very soluble in hot water;slightly soluble in cold water, methanol, ethanol, ethylene glycol, pyridine, acetic acid, and naphtha; and insoluble in acetone, ether, chloroform, and benzene.When heated to decomposition, ethylene thiourea emits toxic fumes of nitrogen oxides (NOx) and sulfur oxides (SOx). Ethylene thiourea is available in the United States as crystals, as a powder, as an 80% dispersion of the powder in oil, or encapsulated in a matrix of compatible elastomers.

Uses

Different sources of media describe the Uses of 96-45-7 differently. You can refer to the following data:
1. Accelerator in the curing of polychloroprene (neoprene) and polyacrylate rubber; intermediate in the manufacture of antioxidants, insecticides, fungicides, dyes, pharmaceuticals, and synthetic resins
2. elastomer accelerator;chlorinated polyethylene (CPE) rubber vulcanizing accelerator agent. Ethylene thiourea is used primarily as an accelerator for vulcanizing polychloroprene (Neoprene?) and polyacrylate rubbers. Neoprene rubbers are used almost exclusively in industrial applications,e.g.. for mechanical and automotive products, in wire and cable production, in construction,and in adhesives. Polyacrylate rubbers are used in products such as seals, o-rings, and gaskets for automotive and aircraft applications. Ethylene thiourea is used in the manufacture of ethylene-bisdithiocarbamate pesticides, such as Maneb?, Mancozeb?, Metiram?,and Zineb?.Ethylene thiourea is also used in electroplating baths, as an intermediate in antioxidant production, in dyes, pharmaceuticals,and synthetic resins. However, there is no evidence that the compound is used commercially for any of these purposes (IARC V.7, 1974; Sax, 1987).
3. 2-Imidazolidinethione is a pesticide used in production of fruits and vegetables. It is also used as a new contrast agent for MRI studies based on proton chemical exchange dependent saturation transfe r. 2-Imidazolidinethione is also a corrosion inhibitor due to the adsorption of the mol. species.

General Description

White to pale green crystals or an off-white solid. Odorless when pure, but technical product may have an amine odor.

Air & Water Reactions

Slightly soluble in water.

Reactivity Profile

Ethlenethiourea may be sensitive to prolonged exposure to light. Incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials generate heat and in many cases hydrogen gas. May react with acids to liberate hydrogen sulfide.

Hazard

Questionable carcinogen.

Health Hazard

Ethylene thiourea (ETU) is an antithyroid substance and animal carcinogen.

Fire Hazard

Ethylene thiourea is combustible.

Flammability and Explosibility

Nonflammable

Contact allergens

Ethylene thiourea, a thiourea derivative, is a rubber chemical. It caused contact dermatitis mainly in rubber workers.

Potential Exposure

Ethylene thiourea is used extensively as an accelerator in the curing of polychloroprene (Neoprene) and other elastomers; as a vulcanizing accelerator in rubber processing; in electroplating baths. In addition, exposure to ethylene thiourea also results from the very widely used ethylene bisdithiocarbamate fungicides. Ethylene thiourea may be present as a contaminant in the ethylene bisdithiocarbamate fungicides and can also be formed when food containing the fungicides is cooked

Carcinogenicity

Ethylene thiourea is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals.

Purification Methods

Crystallise it from EtOH or amyl alcohol. [Beilstein 24 III/IV 22.]

Incompatibilities

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

Waste Disposal

Incineration in a furnace equipped with afterburner and scrubber.

Check Digit Verification of cas no

The CAS Registry Mumber 96-45-7 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 96-45:
(4*9)+(3*6)+(2*4)+(1*5)=67
67 % 10 = 7
So 96-45-7 is a valid CAS Registry Number.
InChI:InChI=1/C3H6N2S/c6-5-2-1-4-3-5/h3,6H,1-2H2

96-45-7 Well-known Company Product Price

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

  • (I504)  2-Imidazolidinethione  98%

  • 96-45-7

  • I504-100G

  • 479.70CNY

  • Detail
  • Aldrich

  • (I504)  2-Imidazolidinethione  98%

  • 96-45-7

  • I504-1KG

  • 1,937.52CNY

  • Detail
  • Sigma-Aldrich

  • (45531)  2-Imidazolidinethione  PESTANAL®, analytical standard

  • 96-45-7

  • 45531-250MG

  • 360.36CNY

  • Detail
  • Sigma-Aldrich

  • (03940)  2-Imidazolidinethione  purum, ≥98.0% (HPLC)

  • 96-45-7

  • 03940-100G

  • 519.48CNY

  • Detail
  • Sigma-Aldrich

  • (03940)  2-Imidazolidinethione  purum, ≥98.0% (HPLC)

  • 96-45-7

  • 03940-500G

  • 1,120.86CNY

  • Detail

96-45-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Imidazolidinethione

1.2 Other means of identification

Product number -
Other names 2-Imidazolidinethione

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Ethylene thiourea is used as an accelerator in synthetic rubber production and as a curing agent for epichlorohydrin elastomers. Ethylene thiourea is also a component of ethylenebisdithiocarbamate fungicides.
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:96-45-7 SDS

96-45-7Relevant articles and documents

Solar-light driven photocatalytic conversion of p-nitrophenol to p-aminophenol on CdS nanosheets and nanorods

Khan, Azam,Rehman, Zia-ur-,Khan, Abdullah,Ambareen, Hina,Ullah, Haseeb,Abbas, Syed Mustansar,Khan, Yaqoob,Khan, Rajwali

, p. 99 - 103 (2017)

A simple synthetic protocol devoid of toxic surfactants was applied for the synthesis of CdS nanosheets and nanorods by thermolyzing bis(4-benzylpiperadine-1-carbodithioate-κ2 S, S′) cadmium(II) (1) and propane-1,3-diyl bis (piperidincarbamodithioate)cadmium(II) (2) using ethylenediamine (en) as a solvent. The as obtained products were characterized by TEM, PXRD, and UV–Visible spectroscopy. The nanosheets (1) and nanorods (2) were confirmed by HR-TEM with a lattice spacing of 0.33?nm which corresponds to the 002 plane of hexagonal CdS, observations in consonance with XRD. Based upon the band gap obtained from UV–Vis, 2.91?eV (nanosheets) and 2.65?eV (nanorods), these nanoparticles (NPs) were used as solar light driven photocatalyst for the conversion of p-nitrophenol to p-aminophenol. The nanorods (8?min) were found slightly more efficient than nanosheets (10?min), and the conversion efficiency of both remained above 92% even after 3rd cycle without any structural damage as revealed by the afterward PXRD. The better catalytic activity of both morphologies can be attributed to quantum size effect and good optical absorbance.

Synthesis method of heterocyclic compound containing bis (trimethylsilyl)

-

Paragraph 0047; 0052-0053; 0056; 0061-0062; 0071; 0073; ..., (2021/09/29)

The method comprises the following steps: first adopting bis (trichloromethyl) carbonate, ethylenediamine, an aqueous sodium hydroxide solution, chloroform and a supported catalyst to obtain 2 - imidazolidinone. Or, ethylenediamine, ethanol, distilled water, a supported catalyst, carbon disulfide and hydrochloric acid are prepared to obtain ethylene thiourea. The trimethylchlorosilane is dissolved in an organic solvent, ammonia gas is introduced, and heated to reflux until no white precipitate is generated and filtered to obtain the filtrate. The raw material 2 - imidazolidinone or ethylidene thiourea is then dissolved to obtain the raw material solution, ammonium sulfate is added, and the filtrate is added dropwise, heated and refluxed 5 - 6h, cooled to room temperature, filtered, and the product is obtained. The molar ratio of the raw material to the trimethyl chlorosilane is 1: (2.1 - 2.5), the quality of ammonium sulfate is 1.5 - 2% of the raw material. The preparation method is simple and high in yield.

An environmentally benign and efficient synthesis of substituted benzothiazole-2-thiols, benzoxazole-2-thiols, and benzimidazoline-2-thiones in water

Liu, Xing,Liu, Min,Xu, Wan,Zeng, Meng-Tian,Zhu, Hui,Chang, Cai-Zhu,Dong, Zhi-Bing

, p. 5591 - 5598 (2017/12/06)

An efficient and practical method for the one-step synthesis of benzothiazole-2-thiols, benzoxazole-2-thiols and benzimidazoline-2-thiones by cyclization of 2-aminothiophenols, 2-aminophenols, and 1,2-phenylenediamines with tetramethylthiuram disulfide (TMTD) in water was described. The features of this method include metal/ligand-free, excellent yield, short reaction time and broad substrate scope. The method provides a facile and convenient preparation of some potentially biologically active compounds.

Synthesis, spectroscopic characterization and in vitro anticancer activity of new platinum(II) complexes with some thione ligands?in the presence of triethylphosphine

Jomaa, Mohammed Yagoub,Altaf, Muhammed,Ahmad, Saeed,Bhatia, Gaurav,Singh, Jatinder,Altuwaijri, Saleh,Isab, Anvarhusein A.

, p. 787 - 795 (2017/10/13)

Seven new platinum(II) complexes (1–7) of triethylphosphine (Et3P) and thiones (L) with general formula, cis-[Pt(Et3P)2(L)2]Cl2 were prepared and characterized by elemental analysis, FTIR and NMR (1H, 13C & 31P) measurements. The analytical and spectroscopic data suggested the formation of the desired complexes. The complexes were tested for in vitro cytotoxicity against four cell lines: Hela (human cervical adenocarcinoma), MCF-7 (human breast carcinoma), A549 (human lung carcinoma), and HTC15 (human colon carcinoma). The anticancer activity values of compounds 1–6 are much better than cisplatin and carboplatin as indicated by their IC50 values.

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