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| | 1,1,3,3-Tetramethoxypropane Basic information |
| Product Name: | 1,1,3,3-Tetramethoxypropane | | Synonyms: | Malonaldehyde bis(dimethyl acetal), 99+%;1,1,3,3-Tetramethoxypropane, 99+%;Malonaldehyde biscdimethyl;Propanedial bis(dimethyl acetal);Malonaldehyde tetramethyl cetal;malonaldehydebis(dimethy acetal);1,1,3,3-TetraMethoxypropane [for BiocheMical Research];Malonaldehyde bis(diMethyl acetal), 99+% 100GR | | CAS: | 102-52-3 | | MF: | C7H16O4 | | MW: | 164.2 | | EINECS: | 203-037-2 | | Product Categories: | Pyridines ,Halogenated Heterocycles;Intermediates;Fine Chemicals;YP00036 | | Mol File: | 102-52-3.mol |  |
| | 1,1,3,3-Tetramethoxypropane Chemical Properties |
| Boiling point | 183 °C (lit.)
70-75 °C/15 mmHg (lit.) | | density | 0.997 g/mL at 25 °C (lit.) | | vapor pressure | 1.7 hPa (20 °C) | | refractive index | n20/D 1.407(lit.) | | Fp | 130 °F | | storage temp. | Store below +30°C. | | solubility | Chloroform, Ethyl Acetate (Slightly) | | form | Liquid | | color | Clear colorless to yellow-brown | | PH | 7 (H2O, 20℃) | | Water Solubility | IMMISCIBLE | | Sensitive | Moisture Sensitive | | BRN | 1700020 | | CAS DataBase Reference | 102-52-3(CAS DataBase Reference) | | NIST Chemistry Reference | Propane, 1,1,3,3-tetramethoxy-(102-52-3) | | EPA Substance Registry System | Propane, 1,1,3,3-tetramethoxy- (102-52-3) |
| Hazard Codes | F | | Risk Statements | 10-36/37/38 | | Safety Statements | 16-26-36/37/39 | | RIDADR | UN 1993 3/PG 3 | | WGK Germany | 1 | | F | 21 | | Hazard Note | Irritant | | TSCA | Yes | | HazardClass | 3 | | PackingGroup | III | | HS Code | 29110000 | | Toxicity | LD50 orally in Rabbit: 2440 mg/kg |
| | 1,1,3,3-Tetramethoxypropane Usage And Synthesis |
| Chemical Properties | clear colourless to yellow-brown liquid | | Uses | 1,1,3,3-Tetramethoxypropane was used in preparing malondialdehyde standards during malondialdehyde assay on lung homogenates. It was used to study the effect of Salvianolic acid A on the migration and proliferation of vascular smooth muscle cells. | | Uses | Organic synthesis. | | General Description | 1,1,3,3-Tetramethoxypropane undergoes acid hydrolysis to yield malondialdehyde. |
| | 1,1,3,3-Tetramethoxypropane Preparation Products And Raw materials |
| Raw materials | 2-Propenal, 3-methoxy-, (2E)--->1,5-DIMETHYL-1,4-CYCLOHEXADIENE-->1,3-Propanediol, 1,3-dimethoxy-, 1,3-diacetate-->3,3-dimethoxypropanal | | Preparation Products | 2-Amino-5-bromonicotinic acid-->2-ACETAMIDOPYRIDINE-3-CARBOXYLIC ACID-->1H-Pyrazolo[3,4-b]pyridine-3-carboxylicacid(9CI)-->2-Bromomalonaldehyde-->3-Methyl-5-nitro-1H-pyrazolo[3,4-b]pyridine ,97%-->1H-Pyrazolo[3,4-b]pyridin-3-amine-->3-NITRO-1H-PYRAZOLO[3,4-B]PYRIDINE-->1-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDE-->1H-PYRAZOLO[3,4-B]PYRIDINE, 3-BROMO--->2-Aminonicotinic acid-->2-Amino-3-cyanopyridine-->1H-Pyrazolo[3,4-b]pyridine,3-methyl-(9CI)-->3-(1H-PYRAZOL-1-YL)BENZOIC ACID-->1H-PYRAZOLO[3,4-B]PYRIDINE-->1-PHENYLPYRAZOLE-->2-PHENYLPYRIMIDINE |
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