2,2-Dimethoxypropane
2,2-Dimethoxypropane Basic information
- Product Name:
- 2,2-Dimethoxypropane
- Synonyms:
-
- Propane, 2,2-dimethoxy-
- Propane,2,2-dimethoxy-
- C.I. 77769
- Dimolybdenum trioxide
- Molybdenum oxide (Mo2O3)
- 2,2-Dimethoxypropane ,98%
- 2,2-DIMETHOXYPROPANE
- ACETONE DIMETHYL ACETAL
- CAS:
- 77-76-9
- MF:
- C5H12O2
- MW:
- 104.15
- EINECS:
- 201-056-0
- Product Categories:
-
- Organics
- Reagents for Oligosaccharide Synthesis
- Biochemistry
- bc0001
- K00001
- Mol File:
- 77-76-9.mol
2,2-Dimethoxypropane Chemical Properties
- Melting point:
- -47 °C
- Boiling point:
- 83 °C (lit.)
- Density
- 0.847 g/mL at 25 °C (lit.)
- vapor density
- 3.59 (vs air)
- vapor pressure
- 60 mm Hg ( 15.8 °C)
- refractive index
- n20/D 1.378(lit.)
- Flash point:
- 12 °F
- storage temp.
- Store below +30°C.
- solubility
- 180g/l
- form
- Liquid
- Specific Gravity
- 0.852 (20/4℃)
- color
- Clear colorless
- explosive limit
- 31%, 58°F
- Water Solubility
- 18 g/100 mL (25 ºC)
- BRN
- 635678
- Stability:
- Stable. Highly flammable - note low flash point. Vapour may form an explosive mixture with air. May form explosive peroxides when exposed to air. Incompatible with strong oxidizing agents.
- InChIKey
- HEWZVZIVELJPQZ-UHFFFAOYSA-N
- CAS DataBase Reference
- 77-76-9(CAS DataBase Reference)
- NIST Chemistry Reference
- 2,2-Dimethoxypropane(77-76-9)
- EPA Substance Registry System
- Propane, 2,2-dimethoxy- (77-76-9)
Safety Information
- Hazard Codes
- F,Xi
- Risk Statements
- 11-36-36/37/38
- Safety Statements
- 26-9-37/39-33-16-33,37/39
- RIDADR
- UN 1993 3/PG 2
- WGK Germany
- 2
- F
- 10-21
- TSCA
- Yes
- HazardClass
- 3
- PackingGroup
- II
- HS Code
- 29110000
- Toxicity
- LD50 orally in Rabbit: > 2260 mg/kg LD50 dermal Rat > 2100 mg/kg
MSDS
- Language:English Provider:Acetone dimethyl acetal
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
2,2-Dimethoxypropane Usage And Synthesis
Chemical Properties
colourless liquid; B.P. 83℃. Ethereal odor. Soluble in alcohol, miscible with ess, oils and perfume chemicals. Stable when pure and at room temp. Decomposes into Acetone and Methanol during heating in presence of moisture or traces of mineral acid. Presumably not used in flavors. Rarely used in perfumes - for ethereal top-notes and "alcohol-like" effects. Produced synthetically via orthoformic ester or vinyl ether. Also from formiminomethyl-ether hydrochloride.
Uses
2,2-Dimethoxypropane(DMP) is used in histology and considered to be more efficient than ethanol for the dehydration of animal tissue.
Uses
2,2-Dimethoxypropane acts as a dehydrating agent. It also serves as an intermediate in the synthesis of vitamin E, vitamin A and various carotenoids such as astaxanthin. It is used as a reagent for the preparation of 1,2-diols, acetonides, isopropylidene derivatives of sugars, nucleosides, methyl esters of amino acids and enol ethers.
General Description
2,2-Dimethoxypropane is an organic compound, which may be used as a protecting agent in the process of the synthesis of structurally related alkaloids like narciclasine and lycoricidine using phenylbromide as the starting material.
2,2-Dimethoxypropane Preparation Products And Raw materials
Preparation Products
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