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828-26-2

2,2,4,4,6,6-Hexamethyl-S-trithiane is a clear colorless to light yellow liquid with a fruity, sulfurous, tangy berry, cooling catty minty black currant, and tropical nuances. It has a taste threshold value of 0.35 to 0.50 ppm and an aroma threshold value of 1.0% EtoH.
Used in Flavor Industry:
2,2,4,4,6,6-Hexamethyl-S-trithiane is used as a flavoring agent for its unique taste and aroma characteristics. It is particularly suitable for enhancing the flavor of fruity, sulfurous, and tangy berry notes in food and beverage products.
Used in Fragrance Industry:
2,2,4,4,6,6-Hexamethyl-S-trithiane is used as a fragrance ingredient for its cooling, catty, and tropical nuances. It can be used in perfumes, colognes, and other scented products to add depth and complexity to the overall scent profile.
Used in Chemical Industry:
2,2,4,4,6,6-Hexamethyl-S-trithiane can be used as a chemical intermediate in the synthesis of various organic compounds. Its unique sulfur-containing structure makes it a valuable building block for the development of new pharmaceuticals, agrochemicals, and other specialty chemicals.

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  • 828-26-2 Structure

  • Basic information

    1. Product Name: 2,2,4,4,6,6-Hexamethyl-S-trithiane
    2. Synonyms: 2,2,4,4,6,6-hexamethyl-s-trithian;2,2,4,4,6,6-Hexamethyl-s-trithiane (trithioacetone);5-trithiane,2,2,4,4,6,6-hexamethyl-3;Hexamethyl-1,3,5-trithiane;Hexamethyl-s-trithiane;s-Trithiane, 2,2,4,4,6,6-hexamethyl-;TRITHIOACETONE;FEMA 3475
    3. CAS NO:828-26-2
    4. Molecular Formula: C9H18S3
    5. Molecular Weight: 222.43
    6. EINECS: 212-582-5
    7. Product Categories: Flavor
    8. Mol File: 828-26-2.mol

  • Chemical Properties

    1. Melting Point: 24 °C(lit.)
    2. Boiling Point: 105-107 °C10 mm Hg(lit.)
    3. Flash Point: 207 °F
    4. Appearance: clear colorless to light yellow liquid
    5. Density: 1.065 g/mL at 25 °C(lit.)
    6. Vapor Pressure: 0.0165mmHg at 25°C
    7. Refractive Index: n20/D 1.54(lit.)
    8. Storage Temp.: Flammables area
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,2,4,4,6,6-Hexamethyl-S-trithiane(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,2,4,4,6,6-Hexamethyl-S-trithiane(828-26-2)
    12. EPA Substance Registry System: 2,2,4,4,6,6-Hexamethyl-S-trithiane(828-26-2)

  • Safety Data

    1. Hazard Codes: Xi,F
    2. Statements: 36/37/38-36/38-11
    3. Safety Statements: 26-37/39-9-33-16
    4. RIDADR: UN 3334
    5. WGK Germany: 2
    6. RTECS: YL8350000
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 828-26-2(Hazardous Substances Data)

828-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 828-26-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 828-26:
(5*8)+(4*2)+(3*8)+(2*2)+(1*6)=82
82 % 10 = 2
So 828-26-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H18S3/c1-7(2)10-8(3,4)12-9(5,6)11-7/h1-6H3

828-26-2SDS

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 2,2,4,4,6,6-Hexamethyl-S-trithiane

1.2 Other means of identification

Product number -
Other names 2,2,4,4,6,6-hexamethyl-1,3,5-trithiane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:828-26-2 SDS

828-26-2Relevant articles and documents

Bis(trimethylsilyl)sulfide based thionation of carbonyl compounds: Synthesis of thioketones

Degl'Innocenti,Capperucci,Mordini,Reginato,Ricci,Cerreta

, p. 873 - 876 (2007/10/02)

A wide range of thioketones may be conveniently obtained by silyl triflate promoted bis(trimethylsilyl)sulfide thionation of ketones.

Thiocyanohydrins, a new class of compounds, precursors of unstabilized thiocarbonyl derivatives

Gaumont,Wazneh,Denis

, p. 4927 - 4940 (2007/10/02)

Mono- and dialkylated thiocyanohydrins are prepared by alkylation of the parent compound 2 (NCCH2SH) under mild conditions. Some examples of the reactivity of this new class of compounds are also given.

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