1779-19-7

• 

• Basic information

  1. Product Name: 1,3,6-TRIOXACYCLOOCTANE
  2. Synonyms: 1,3,6-Trioxocane;1,3,6-Trioxocin, tetrahydro-;Diethylene glycol formal;Diglycol formal;1,3,6-TRIOXACYCLOOCTANE
  3. CAS NO:1779-19-7
  4. Molecular Formula: C₅H₁₀O₃
  5. Molecular Weight: 118.13
  6. EINECS: 217-215-2
  7. Product Categories: N/A
  8. Mol File: 1779-19-7.mol
  9. Article Data: 7

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 165℃
  3. Flash Point: 51.3oC
  4. Appearance: /
  5. Density: 1.026g/cm3
  6. Vapor Pressure: 2.54mmHg at 25°C
  7. Refractive Index: 1.4423 (589.3 nm 20℃)
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 1,3,6-TRIOXACYCLOOCTANE(CAS DataBase Reference)
  11. NIST Chemistry Reference: 1,3,6-TRIOXACYCLOOCTANE(1779-19-7)
  12. EPA Substance Registry System: 1,3,6-TRIOXACYCLOOCTANE(1779-19-7)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 1779-19-7(Hazardous Substances Data)

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• 1,3,6-TRIOXACYCLOOCTANE CAS 1779-19-7

  Cas No: 1779-19-7

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• 1,3,6-TRIOXACYCLOOCTANE CAS:1779-19-7

  Cas No: 1779-19-7

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1779-19-7 Usage

General Description

1,3,6-Trioxacyclooctane, also known as 1,3,6-Trioxacyclooctane or cyclotrioxane, is a cyclic ether compound with the chemical formula C6H12O3. It is a colorless liquid with a faint odor, and it is not soluble in water but is miscible with most organic solvents. This chemical is mainly used as a solvent and as a starting material for the synthesis of other organic compounds. It is also used as a reagent in organic chemistry reactions. 1,3,6-Trioxacyclooctane is considered to be a relatively stable compound and does not pose significant health risks or environmental concerns. Overall, it is a versatile chemical with various industrial and laboratory applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1779-19-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,7 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1779-19:
(6*1)+(5*7)+(4*7)+(3*9)+(2*1)+(1*9)=107
107 % 10 = 7
So 1779-19-7 is a valid CAS Registry Number.

InChI:InChI=1/C5H10O3/c1-3-7-5-8-4-2-6-1/h1-5H2

1779-19-7SDS

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	1,3,6-trioxocane

1.2 Other means of identification

Product number	-
Other names	1,3,6-Trioxacyclooctane

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:1779-19-7 SDS

1779-19-7Upstream product

• 50-00-0 formaldehyd 
• 111-46-6 diethylene glycol 
• 75-21-8 oxirane 
• 646-06-0 1,3-DIOXOLANE 

1779-19-7Downstream Products

1779-19-7Relevant articles and documents

Miscible Polyether/Poly(ether-acetal) Electrolyte Blends

Gao, Kevin W.,Loo, Whitney S.,Snyder, Rachel L.,Abel, Brooks A.,Choo, Youngwoo,Lee, Andrew,Teixeira, Susana C. M.,Garetz, Bruce A.,Coates, Geoffrey W.,Balsara, Nitash P.

, p. 5728 - 5739 (2020)

This study shows that it is possible to obtain homogeneous mixtures of two chemically distinct polymers with a lithium salt for electrolytic applications. This approach is motivated by the success of using mixtures of organic solvents in modern lithium-io

A method for preparing 1, 3 - oxa naphthenic (by machine translation)

-

Paragraph 0096-0099; 0102; 0106; 0110; 0114; 0118; 0123, (2019/05/16)

The invention discloses a 1, 3 - oxa naphthenic preparation method, the method comprises: diol, poly formaldehyde in water and ionic liquid catalyst in the presence of a cyclization reaction, containing the reaction product of the compound; wherein said diol is ethylene glycol or diethylene glycol; when the diol is ethylene glycol when, the target compound is 1, 3 - dioxolo; when the diol is diethylene glycol when, the target compound is 1, 3, 6 - heterocyclic octane; the ionic liquid catalyst comprises a cation and anion, the cation is selected from the isoquinoline kind of positive ion, quinoline kind of positive ion and benzimidazole in at least one of the kind of positive ion. The method of the invention the kind of positive ion cation is isoquinoline, quinoline kind of positive ion or benzimidazole kind of positive ion of the ionic liquid as catalyst to prepare 1, 3 - oxa naphthenic, mild reaction conditions, high product yield, catalyst is environment-friendly. (by machine translation)

Novel ring-expansion reaction between cyclic formal and ethylene oxide

Yamasaki, Naoaki,Nagahara, Hajime,Masamoto, Junzo

, p. 271 - 274 (2007/10/03)

Novel direct reactions between trioxane and ethylene oxide were discovered, and three novel cyclic formals were isolated and identified. These novel cyclic compounds clarified the initiation mechanism of the copolymerization of trioxane and ethylene oxide

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