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1,2,4,5-tetrathiane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

291-22-5

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291-22-5 Usage

Molecular structure

Four carbon atoms and four sulfur atoms arranged in a ring

Physical state

Colorless liquid

Odor

Strong, unpleasant

Flammability

Highly flammable

Solvent

Commonly used in chemical reactions

Reagent

Used in organic synthesis

Corrosion inhibitor

Utilized to prevent corrosion

Pesticide production

Employed in the manufacturing process

Pharmaceutical potential

Studied for possible applications in the pharmaceutical industry

Materials science

Investigated for its unique structure and properties in materials science

Toxicity

Can be toxic and hazardous to health

Environmental impact

Hazardous to the environment

Safety precautions

Handle with care and follow safety guidelines

Check Digit Verification of cas no

The CAS Registry Mumber 291-22-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,9 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 291-22:
(5*2)+(4*9)+(3*1)+(2*2)+(1*2)=55
55 % 10 = 5
So 291-22-5 is a valid CAS Registry Number.

291-22-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,4,5-tetrathiane

1.2 Other means of identification

Product number -
Other names 1,2,4,5-Tetrathiacyclohexane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:291-22-5 SDS

291-22-5Downstream Products

291-22-5Relevant academic research and scientific papers

CYCLIC POLYSULPHIDES FROM PARKIA SPECIOSA

Gmelin, R.,Susilo, R.,Fenwick, G. R.

, p. 2521 - 2524 (1981)

Five polysulphides have been isolated from Parkia speciosa.The structures of four of these have been established as 1,2,4-trithiolane, 1,2,4,6-tetrathiepane, 1,2,3,5,6-pentathiepane (lenthionine) and 1,2,4,5,7,8-hexathionane.A further product has been tentatively assigned either the 1,2,4,6,7- or 1,2,4,5,7-pentathiocane structure.Key Word Index - Parkia speciosa; Mimosaceae; cyclic polysulphides; lenthionine.

Changes in the Key Aroma Compounds of Raw Shiitake Mushrooms (Lentinula edodes) Induced by Pan-Frying As Well As by Rehydration of Dry Mushrooms

Schmidberger, Philipp C.,Schieberle, Peter

, p. 4493 - 4506 (2020)

Application of the aroma extract dilution analysis (AEDA) on an extract/distillate from raw shiitake mushrooms revealed 32 odorants among which 3-(methylthio)propanal (cooked potato), 1-octen-3-one, and 1-octen-3-ol (both mushroom-like) showed the highest flavor dilution (FD) factors. An isotope enrichment experiment with raw shiitake tissue and either 13C18-linoleic acid or 2H4-1-octen-3-ol confirmed that both 1-octen-3-ol and 1-octen-3-one are direct degradation products of the fatty acid, but it could be proven for the first time that the ketone is not formed by an oxidation of the alcohol. After pan-frying, 42 odor-active compounds appeared among which 3-hydroxy-4,5-dimethylfuran-2(5H)-one (savory), 1,2,4,5-tetrathiane (burnt, sulfury), 4-hydroxy-2,5-dimethylfuran-3(2H)-one (caramel-like), phenylacetic acid (honey-like), 3-(methylthio)-propanal, and trans-4,5-epoxy-(E)-2-decenal (metallic) showed the highest FD factors. To get a deeper insight into their aroma contribution, 19 key odorants were quantitated in the raw shiitake and twenty-one in the pan-fried mushrooms by stable isotope dilution assays, and new methods for the quantitation of four sulfur compounds were developed. A calculation of odor activity values (OAV; ratio of concentration to odor threshold) showed that 1-octen-3-one was by far the most important odorant in raw shiitake. During pan-frying, in particular, four aroma compounds were significantly increased, i.e., 4-hydroxy-2,5-dimethylfuran-3(2H)-one, dimethyl trisulfide, 1,2,4,5-tetrathiane, and 1,2,3,5,6-pentathiepane. The overall aroma profile of pan-fried shiitake could very well be mimicked by an aroma recombinate consisting of 15 reference aroma compounds in the concentrations determined in the pan-fried mushrooms. Further results showed that the sulfur compounds were even higher in rehydrated dry shiitake as compared to the pan-fried mushrooms.

COMPOSITION FOR OPTICAL MATERIAL AND OPTICAL MATERIAL USING THE SAME

-

Paragraph 0100-0102, (2018/05/24)

The present invention provides a composition for an optical material containing a ring compound (a) represented by formula (1), an episulfide compound (b), and sulfur (c), wherein the content of the ring compound (a) in the composition for an optical material is in the range of 5-70 mass %, the content of the episulfide compound (b) is in the range of 20-90 mass %, and the content of the sulfur (c) is in the range of 1-39 mass %. (In the formula, X represents S, Se or Te. a to f=0 to 3, 8≥(a+c+e)≥1, 8≥(b+d+f)≥2, and (b+d+f)≥(a+c+e).) This composition for an optical material has a high refractive index as an optical characteristic, and has sufficient heat resistance and good mold release characteristics.

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