122174-81-6

Basic information

• Product Name: O¹,O⁶-dibenzoyl-O²,O⁴;O³,O⁵-dimethanediyl-D-iditol
• CAS NO: 122174-81-6
• Molecular Weight: 414.412
• Mol File: 122174-81-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: O¹,O⁶-dibenzoyl-O²,O⁴;O³,O⁵-dimethanediyl-D-iditol(CAS DataBase Reference)
• NIST Chemistry Reference: O¹,O⁶-dibenzoyl-O²,O⁴;O³,O⁵-dimethanediyl-D-iditol(122174-81-6)
• EPA Substance Registry System: O¹,O⁶-dibenzoyl-O²,O⁴;O³,O⁵-dimethanediyl-D-iditol(122174-81-6)

Safety Data

• Hazardous Substances Data: 122174-81-6(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 7226-27-9 1,6-di-O-benzoyl-D-mannitol 
• 98-88-4 benzoyl chloride 
• 5334-20-3 2,4:3,5-di-O-methylene-D-glucitol 
• 886597-56-4 O²,O⁴;O³,O⁵-dimethanediyl-allitol 
• 488-44-8 allitol 
• 5334-20-3 2,4:3,5-di-O-methylene-L-iditol 

Downstream Products

• 5349-04-2 O¹,O⁶-diacetyl-O²,O⁴;O³,O⁵-dimethanediyl-D-mannitol 
• 114202-83-4 O¹,O⁶-dibenzoyl-O²,O⁴-methanediyl-D-glucitol 
• 4539-77-9 2,4:3,5-Di-O-methylen-D-glucarsaeure-dimethylester 
• 5349-04-2 O¹,O⁶-diacetyl-O²,O⁴;O³,O⁵-dimethanediyl-D-glucitol 
• 3013-59-0 (4R,5R,6S)-4-<(1R)-1,2-Dihydroxyethyl>-5-hydroxy-6-hydroxymethyl-1,3-dioxane 
• 119659-39-1 O⁵-acetyl-O¹,O³,O⁶-tribenzoyl-O²,O⁴-methanediyl-D-glucitol 
• 122147-88-0 O³,O⁵-diacetyl-O¹,O⁶-dibenzoyl-O²,O⁴-methanediyl-D-glucitol 
• 124107-94-4 O⁵-acetyl-O¹,O⁶-dibenzoyl-O²,O⁴-methanediyl-O³-methyl-D-glucitol 
• 121965-38-6 O³-acetoxymethyl-O⁵-acetyl-O¹,O⁶-dibenzoyl-O²,O⁴-methanediyl-D-glucitol 
• 5334-20-3 2,4:3,5-di-O-methylene-D-glucitol 
• 121315-58-0 O¹,O⁵,O⁶-tribenzoyl-O²,O⁴-methanediyl-D-glucitol 
• 114843-20-8 O⁵-acetyl-O¹,O⁶-dibenzoyl-O²,O⁴-methanediyl-D-glucitol 

Relevant articles and documents

Partially renewable copolyesters prepared from acetalized d -glucitol by solid-state modification of poly(butylene terephthalate)

The backbone of poly(butylene terephthalate) (PBT) was modified with 2,4:3,5-di-O-methylene-D-glucitol (Glux) using solid-state modification (SSM). The obtained copolyesters proved to have a non-random overall chemical microstructure. The thermal properties of these semicrystalline, block-like, Glux-based materials were extraordinary, showing higher melting points, and glass transition temperatures compared with other sugar-based copolyesters prepared by SSM. These remarkable thermal properties were a direct result of the inherently rigid structure of Glux and the relatively slow randomization of the block-like chemical microstructure of the Glux-based copolyesters in the melt. SSM proved to be a versatile tool for preparing partially biobased copolyesters with superior thermal properties. Copyright