PARAFORMALDEHYDE

HCID 178665535CAS 25231-38-3

Basic information

Standard SMILES
CC(=O)OCOC(C)=O
InChIKey
BPGDAMSIGCZZLK-UHFFFAOYSA-N
Molecular formula
C3H6O3X2
Average molar mass
90.08 g/mol

Names & identifiers

Preferred name
PARAFORMALDEHYDE
English name
PARAFORMALDEHYDE
Molecular formula
C3H6O3X2
Molecular weight
90.08

Names & synonyms

POLYFORMALDEHYDEPOLYACETALPARAFORMACETAL RESINPOLY(TRIOXANE)POLYOXMETHYLENEPOLYACETAL RESINFORMALDEHYDE RESINPolyoxymethylenediacetateoxymethylene homopolymer diacetate

Database identifiers

CAS
25231-38-3

Properties

Physicochemical properties

Melting point
175 °C · 175 °C
Density
1.42 g/mL · 1.42 g/mL at 25 °C
vapor density
1.03 · 1.03 (vs air)
vapor pressure
1.45 mm · <1.45 mm Hg ( 25 °C)
Flash point
158 °F · 158 °F
solubility
70 °C: · chlorophenol above 70°C: soluble

Safety & regulation

Safety data

wgk
3
tsca
TSCA listed
rtecs
RV0540000
ridadr
UN 2213 4.1/PG 3
risk_code
31
hazard_code
Xn

Chemistry & industry

Preparation methods · 1 item

Preparation(a) Homopolymers In the preparation of high molecular weight polyformaldehyde the initial operation consists of the production of pure formaldehyde, free from low molecular weight polymers and other hydroxy compounds which cause chain transfer. In a typical process potassium hydroxide-precipitated paraformaldehyde (degree of polymerization approximately 200) is carefully washed with water and dried for several hours in vacuo at 80C. The dried polymer is then decomposed in nitrogen at 150-160C; the product is passed through several traps at -15C to remove water, glycols, and other impurities. The resulting formaldehyde has a water content (free and combined) of less than 0.1 %.The formaldehyde is then introduced into a reactor where it passes over the surface of a rapidly stirred solution of initiator (either a Lewis acid or base; triphenylphosphine appears to be favoured) in a carefully dried inert medium such as heptane at about 40C. The process is designed to give a very low concentration of formaldehyde to minimize transfer from polymer to monomer. To the initiator solution may be added a polymer stabilizer (e.g. diphenylamine) and transfer agents (e.g. traces of water or methanol). Polymerization is continued until the concentration of polymer in the slurry is about 20% and then the polymer is collected by filtration.In the final stage the polymer is subjected to an esterification reaction to improve its thermal stability. The esterification may be effected with a number of anhydrides, but acetic anhydride is generally preferred. Typically, the polyformaldehyde is heated under slight pressure to about 160C with acetic anhydride and a small amount of sodium acetate (catalyst). The polymer is soluble in acetic anhydride at this temperature but is precipitated when the solution is cooled. The acetylated polymer is collected by filtration, washed with water (to remove the anhydride and catalyst) and then acetone (containing di-fi-naphthyl-p-phenylenediamine as antioxidant), and dried in vacuo at 70C. The product is then extruded and chopped into granules. The average molecular weight (Mn) of the polyformaldehyde produced by these methods is generally in the range 30000-100000.The polymerization of formaldehyde by Lewis bases such as triaryl amines (R3N), arsines, and phosphines proceeds by the following anionic mechanism:The polymerization of formaldehyde by Lewis acids such as boron trifluoride proceeds according to following cationic mechanism:The hydroxy-terminated polymers have poor thermal stability. Loss of a proton, possibly to an initiator residue, from a chain end gives an anion

Suppliers9 total

上海赛可锐生物科技有限公司021-58000709 13120558703 · [email protected]
上海维亦特生物科技有限公司15317051735 · [email protected]
广东元丰化学试剂有限公司0751-2829979 13376591640 · [email protected]
广东翁江化学试剂有限公司0751-2815987 13927875076 · [email protected]
陕西缔都医药化工有限公司029-029-81120477 17792793610 · [email protected]

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