FEMA 2129

FEMA 2129 Suppliers list
Company Name: Nanjing Dolon Biotechnology Co.,Ltd.
Tel: 18905173768
Email: sales@dolonchem.com
Products Intro: CAS:1319-88-6
Company Name: CONIER CHEM AND PHARMA LIMITED
Tel: +8618523575427
Email: sales@conier.com
Products Intro: Product Name:BENZALDEHYDE GLYCERYL ACETAL
CAS:1319-88-6
Purity:99% Package:1kg
Company Name: SIMAGCHEM CORP
Tel: +86-13806087780
Email: sale@simagchem.com
Products Intro: Product Name:Benzaldehyde Glycrol Acetal
CAS:1319-88-6
Purity:0.99 Package:1kg,5kg,25kgs,200kgs;bulk
Company Name: Career Henan Chemica Co
Tel: +86-0371-86658258 15093356674;
Email: laboratory@coreychem.com
Products Intro: Product Name:FEMA 2129
CAS:1319-88-6
Purity:99% Package:1KG;9.20USD
Company Name: ANHUI WITOP BIOTECH CO., LTD
Tel: +8615255079626
Email: eric@witopchemical.com
Products Intro: Product Name:Benzaldehyde, cyclic acetal with 1,2,3-propanetriol
CAS:1319-88-6
FEMA 2129 Basic information
Product Name:FEMA 2129
Synonyms:Benzaldehyde,cyclicacetalwith1,2,3-propanetriol;BENZAL GLYCERYL ACETAL;BENZALDEHYDE GLYCERYL ACETAL;FEMA 2129;Benzyl glyceryl acetal;5-Hydroxy-2-phenyl-1,3-dioxan;Benzalglycerin;Benzaldehyde glycrol acetal
CAS:1319-88-6
MF:C10H12O3
MW:180.2
EINECS:215-294-8
Product Categories:
Mol File:1319-88-6.mol
FEMA 2129 Structure
FEMA 2129 Chemical Properties
Boiling point 152-154 °C(Press: 12 Torr)
density 1.2115 g/cm3(Temp: 25 °C)
FEMA 2129 | BENZALDEHYDE GLYCERYL ACETAL
color A colourless viscous liquid.
Odorat 100.00 %. cherry bitter almond sweet
Odor Typefruity
JECFA Number838
LogP1.98
EPA Substance Registry SystemBenzaldehyde, cyclic acetal with 1,2,3-propanetriol (1319-88-6)
Safety Information
toxicityThe acute oral LD50 value in rats was reported as 3?5 ml/kg (2.42-4.09 ml/kg) and the acute dermal LD50 value in rabbits as 5 ml/kg
MSDS Information
FEMA 2129 Usage And Synthesis
OccurrenceHas apparently not been reported to occur in nature
PreparationThe α, α?- and α, β-isomers are obtained in mixture by heating glycerol and benzaldehyde to 145 to 170°C under a stream of CO2; the isomers are subsequently isolated, exploiting the solubility differences; the α, α?-isomer is readily converted to the α, β-form by heating in the presence of HCl.
FEMA 2129 Preparation Products And Raw materials
Tag:FEMA 2129(1319-88-6) Related Product Information
Ketoconazole FEMA 2129 (+)-2,3-O-BENZYLIDENE-D-THREITOL cis-[2-(2,4-Dichlorophenyl)-2-(1H-imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methyl-4-methylbenzenesulphonate 1,3-Dioxolane-4-methanol (-)-DIMETHYL 2,3-O-BENZYLIDENE-L-TARTRATE (+)-4,5-BIS[HYDROXY(DIPHENYL)METHYL]-2-METHYL-2-PHENYL-1,3-DIOXOLANE THYMELEATOXIN MEZEREIN (2R,3R)-2,3-O-(1-PHENYLETHYLIDENE)-L-TARTARIC ACID DIMETHYL ESTER Methyl 2,3:4,6-Di-O-benzylidene-α-D-mannopryanoside 2-(2,4-DICHLOROPHENYL)-2-(1H-IMIDAZOL-1-YL METHYL)-1,3-DIOXOLANE-4-METHANOL 2-(2,4-DICHLOROPHENYL)-2-(1,2,4-TRIAZOL-1-YL METHYL)-1,3-DIOXALANE-4-YL METHYL METHANE SULFONATE (-)-2,3-O-BENZYLIDENE-L-THREITOL Doconazole BENZYLIDENE CBZ-NEURAMINIC ACID 2-METHYL-2-PHENYL-4-[(PROP-2-YNYLOXY)METHYL]-1,3-DIOXOLANE 2-PHENYL-4-[(PROP-2-YNYLOXY)METHYL]-1,3-DIOXOLANE