ChemicalBook > CAS DataBase List > 1,3,5-trioxane

1,3,5-trioxane

Product Name
1,3,5-trioxane
CAS No.
110-88-3
Chemical Name
1,3,5-trioxane
Synonyms
Trioxane;S-TRIOXANE;TRIOXYMETHYLENE;1,3,5-Trioxan;Trioxan;Paraformal;SYM-TRIOXANE;Trioxymethylen;1,3,5-TRIOXACYCLOHEXANE;Trioxin
CBNumber
CB5763739
Molecular Formula
C3H6O3
Formula Weight
90.08
MOL File
110-88-3.mol
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1,3,5-trioxane Property

Melting point:
59-62 °C(lit.)
Boiling point:
112-115 °C
Density 
1.17
vapor pressure 
7.5 hPa (20 °C)
refractive index 
1.4168 (estimate)
Flash point:
113 °F
storage temp. 
Store below +30°C.
solubility 
221g/l
form 
Crystals or Crystalline Flakes
color 
Colorless to white
explosive limit
3.6-28.7%(V)
Water Solubility 
221 g/L (25 ºC)
Sublimation 
115 ºC
Merck 
14,9734
BRN 
102769
InChIKey
BGJSXRVXTHVRSN-UHFFFAOYSA-N
CAS DataBase Reference
110-88-3(CAS DataBase Reference)
NIST Chemistry Reference
1,3,5-Trioxane(110-88-3)
EPA Substance Registry System
1,3,5-Trioxane (110-88-3)
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Safety

Hazard Codes 
F,Xn
Risk Statements 
11-37-63
Safety Statements 
36/37-46
RIDADR 
UN 1325 4.1/PG 2
WGK Germany 
1
RTECS 
YK0350000
Autoignition Temperature
777 °F
TSCA 
Yes
HS Code 
2912 50 00
HazardClass 
4.1
PackingGroup 
III
Hazardous Substances Data
110-88-3(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: 8190 mg/kg LD50 dermal Rabbit > 3980 mg/kg
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H228Flammable solid

H335May cause respiratory irritation

Precautionary statements

P201Obtain special instructions before use.

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P308+P313IF exposed or concerned: Get medical advice/attention.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
T81108
Product name
1,3,5-Trioxane
Purity
≥99%
Packaging
25g
Price
$24.6
Updated
2024/03/01
Sigma-Aldrich
Product number
T81108
Product name
1,3,5-Trioxane
Purity
≥99%
Packaging
2kg
Price
$153
Updated
2024/03/01
Sigma-Aldrich
Product number
8.21189
Product name
1,3,5-Trioxane
Purity
for synthesis
Packaging
100g
Price
$35.5
Updated
2024/03/01
Sigma-Aldrich
Product number
8.21189
Product name
1,3,5-Trioxane
Purity
for synthesis
Packaging
1kg
Price
$91.5
Updated
2024/03/01
Sigma-Aldrich
Product number
8.21189
Product name
1,3,5-Trioxane
Purity
for synthesis
Packaging
25kg
Price
$1200
Updated
2024/03/01
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1,3,5-trioxane Chemical Properties,Usage,Production

Chemical Properties

Paraformaldehyde is a white crystalline solid. Irritating odor. The term “trioxane” applies specifically to this trimer (CH2O)3 but paraformaldehyde is applied both to trioxane and other low polymers or oligomers of formaldehyde.

Chemical Properties

Trioxane is a most unusual chemical. It is an excellent solvent for many classes of materials. Concentrated aqueous solutions of trioxane have solvent properties which are not possessed by trioxane itself. Molten trioxane dissolves numerous organic compounds, such as naphthalene, urea, camphor, dichlorobenzene, etc. It is stable in alkaline or neutral solutions, yet it is depolymerized to formaldehyde by small amounts of strong acid or acid-forming materials, and the rate of depolymerization can be readily controlled.

Uses

1,3,5-Trioxane is used in organic chemical processes such as aldol condensation of amides and syntheses of chloromethyl esters or other plastics.

Uses

1,3,5-Trioxane is widely used as a source of anhydrous formaldehyde.
It can be used to synthesize:

  • Polyoxymethylene and hyperbranched polyesters.
  • Calixarenes such as calix[4]resorcinarene, calix[6]resorcinarene and para-tert-butylcalix[8] and [9]arene.
  • Various natural products including (?)-motuporin, (+)-sundiversifolide, (+)-lyconadin A and (?)-lyconadin B.

Definition

ChEBI: A saturated organic heteromonocyclic parent that is cyclohexane in which the carbon atoms at positions 1, 3 and 5 are replaced by oxygen atoms.

General Description

Transparent crystals or white crystalline solid with a pleasant odor resembling the odor of chloroform. Melts at 62°C; boils at 115°C without polymerization. The cyclic trimer of formaldehyde.

Air & Water Reactions

Highly flammable. Water soluble.

Reactivity Profile

s-Trioxane is stable under normal laboratory conditions but is unstable in the presence of acids, which initiate polymerization. Sublimes readily. May react with oxidizing matter . A stable polymeric product of formaldehyde that in the presence of strong aqueous acids will depolymerize (reforming the parent formaldehyde). Inert to strong alkalis. Readily converted in non aqueous solutions to the monomeric formaldehyde by small concentrations of acid---the rate of conversion is directly proportional to the concentration of the acid.

Health Hazard

ACUTE/CHRONIC HAZARDS: s-Trioxane is toxic and flammable. It can emit toxic fumes on contact with acid or acid fumes.

Fire Hazard

s-Trioxane is combustible.

Safety Profile

Mutation data reported. Can evolve toxic formaldehyde fumes when heated strongly or in contact with strong acids or acid fumes. Flammable liquid when exposed to heat, flame, or oxidzers. May explode when heated. Explosive in the form of vapor when exposed to heat or flame. Explodes on impact, possibly due to peroxide contamination. Mixtures with hydrogen peroxide are explosives sensitive to heat, shock, or contact with lead. Mixtures with liquid oxygen are highly explosive. Incompatible with oxidizing materials. To fight fire, use foam, CO2, or dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes. See also FORMALDEHYDE.

Potential Exposure

Paraformaldehyde is used in polyacetal resin manufacture; as a food additive; and as an odorless fuel.

Shipping

UN2213 Paraformaldehyde, Hazard Class: 4.1; Labels: 4.1-Flammable solid.

Purification Methods

Crystallise 1,3,4-trioxane from sodium-dried diethyl ether or water, and dry it over CaCl2. It can also be purified by zone refining. [Beilstein 19 H 381, 19 II 392, 19 III/IV 4710, 19/9 V 103.]

Incompatibilities

Paraformaldehyde dust forms an explosive mixture with air. Decomposes on contact with oxidizers, strong acids; acid fumes; and bases; with elevated temperatures, forming formaldehyde. May explode when heated. May explode on impact if peroxide contamination develops. Mixtures with hydrogen peroxide or liquid oxygen are explosives sensitive to heat, shock, or contact with lead.

Waste Disposal

Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.

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View Lastest Price from 1,3,5-trioxane manufacturers

Hebei Fengqiang Trading Co., LTD
Product
1,3,5-trioxane 110-88-3
Price
US $100.00/drum
Min. Order
1drum
Purity
99
Supply Ability
5000
Release date
2023-09-12
Hebei Guanlang Biotechnology Co., Ltd.
Product
1,3,5-trioxane 110-88-3
Price
US $10.00/KG
Min. Order
100KG
Purity
99%
Supply Ability
100 mt
Release date
2021-08-09
Zhuozhou Wenxi import and Export Co., Ltd
Product
1,3,5-Trioxane 110-88-3
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-06-27

110-88-3, 1,3,5-trioxaneRelated Search:


  • 1,3,5-Trioxan
  • 1,3,5-TRIOXACYCLOHEXANE
  • 1,3,5-TRIOXANE
  • TRIOXYMETHYLENE
  • TRIFORMOL
  • 1,3,5-trioxane (sym.)
  • Formaldehyde trimer~s-Trioxan
  • METAFORMALDEHYDE
  • S-TRIOXAN
  • S-TRIOXANE
  • SYM-TRIOXANE
  • 1,3,5-TRIOXANE, 99+%
  • s-Trioxane, 99.5+%
  • 1,3,5-trioxan trioxymethylene
  • Metaformaldehyde, sym.-Trioxane, Trioxymethylene
  • s-Trioxane, 99+%
  • s-Trioxane, 99.5+% 2KG
  • s-Trioxane, 99.5+% 500GR
  • 1,3,5-Trioxane 〔Trioxymethylene〕
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  • Formaldehyde, trimer
  • formaldehyde,trimer
  • Marvosan
  • Metaformaldehyd
  • Paraformal
  • s-Tioxane
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  • Triossimetilene
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  • Trioxin
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  • Trioxymethylen
  • 1,3,5-Trioxane&gt
  • 1,3,5-TRIOXANE FOR SYNTHESIS 1 KG
  • 1,3,5-TRIOXANE FOR SYNTHESIS 100 G
  • 1,3,5-trioxane ISO 9001:2015 REACH
  • 1,3,5-TRIOXANE For Synthesis
  • 1,3,5-Trioxane, ≥ 99.0%
  • 110-88-3
  • 110883
  • HCHO3
  • Acetals/Ketals/Ortho Esters
  • Organic Building Blocks
  • Oxygen Compounds
  • Building Blocks
  • Acetals/Ketals/Ortho Esters
  • Building Blocks
  • Chemical Synthesis
  • Organic Building Blocks
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