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2,2-Dimethoxypropane structure

2,2-Dimethoxypropane

  • CAS:77-76-9
  • MW:104.14758
  • MF:C5H12O2
2,2-Dimethoxypropane(DMP) is used in histology and considered to be more efficient than ethanol for the dehydration of animal tissue. 2,2-Dimethoxypropane Preparation Products And Raw materials Preparation Products View more+
 
1. Names and Identifiers
1.1 Name
2,2-Dimethoxypropane
1.2 Synonyms
2,2-Dimethyoxypropane; ACETONE DIMETHYL ACETAL; ACETONE DIMETHYL KETAL; acetone dimethylacetal; Acetone-dimethyl acetal; C.I. 77769; Dimolybdenum trioxide; EINECS 201-056-0; MFCD00008479; Molybdenum oxide (Mo2O3); Propane, 2,2-dimethoxy-; Propane,2,2-dimethoxy-;
1.3 CAS No.
77-76-9
1.4 CID
6495
1.5 EINECS
201-056-0
1.6 Molecular Formula
C5H12O2
1.7 Inchi
InChI=1S/C5H12O2/c1-5(2,6-3)7-4/h1-4H3
1.8 InChkey
HEWZVZIVELJPQZ-UHFFFAOYSA-N
1.9 Canonical Smiles
CC(C)(OC)OC
1.10 Isomers Smiles
CC(C)(OC)OC
2. Properties
2.1 Vapour pressure
3.59 (vs air)
2.2 Solubility
180g/l
2.3 VaporDensity
3.59 (vs air)
2.4 Appearance
Clear colorless Liquid
2.5 Atmospheric OH Rate Constant
3.92e-12 cm3/molecule*sec
2.6 Storage
Ambient temperatures.
2.7 Chemical Properties
colourless liquid
2.8 Color/Form
Clear colorless
2.9 Water Solubility
H2O: 18 g/100 mL (25 oC)
2.10 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.
2.11 StorageTemp
Store below +30°C.
3. Use and Manufacturing
3.1 Description

colourless liquid


2,2-Dimethoxypropane or acetone dimethyl acetal or DMP is an organic compound and an alkylating reagent. The chemical formula is C5H12O2 and the molecular formula is (CH3)2C(OCH3)2. It is the acetalisation product of acetone and methanol. Dimethoxypropane is an intermediate for the synthesis of 2-methoxypropene. In histology, DMP is now considered to be more efficient than ethanol for the dehydration of animal tissue.

3.2 Usage
2,2-Dimethoxypropane(DMP) is used in histology and considered to be more efficient than ethanol for the dehydration of animal tissue. 2,2-Dimethoxypropane Preparation Products And Raw materials Preparation Products
4. Safety and Handling
4.1 Safety

A very dangerous fire hazard when exposed to heat, flame or oxidizers. When heated to 210°C it burns with a cool flame and then explodes. Explosive reaction with metal perchlorates (e.g., manganese(II) perchlorate; nickel(II) perchlorate) above 65°C. When heated to decomposition it emits acrid smoke and fumes.
Hazard Codes? FFlammable,XiIrritant
Risk Statements? 11-36-36/37/38?
R11:Highly flammable.?
R36:Irritating to eyes.?
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements? 26-9-37/39-33-16-33,37/39?
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.?
S9:Keep container in a well-ventilated place.?
S37/39:Wear suitable gloves and eye/face protection.?
S33:Take precautionary measures against static discharges.?
S16:Keep away from sources of ignition.?
S37/39:Wear suitable gloves and eye/face protection.
RIDADR? UN 1993 3/PG 2
WGK Germany? 2
F? 10-21
HazardClass? 3
PackingGroup? II
HS Code? 29110000

4.2 Specification

?2,2-Dimethoxypropane , its CAS NO. is 77-76-9, the synonyms are Acetone dimethyl acetal ; Acetone dimethyl ketal ; Propane, 2,2-dimethoxy- .

4.3 Toxicity
LD50 orally in Rabbit: > 2260 mg/kg LD50 dermal Rat > 2100 mg/kg
5. MSDS

2.Hazard identification

2.1 Classification of the substance or mixture

Flammable liquids, Category 2

Skin irritation, Category 2

Eye irritation, Category 2

Specific target organ toxicity \u2013 single exposure, Category 3

2.2 GHS label elements, including precautionary statements

Pictogram(s)
Signal word

Danger

Hazard statement(s)

H225 Highly flammable liquid and vapour

H315 Causes skin irritation

H319 Causes serious eye irritation

H335 May cause respiratory irritation

Precautionary statement(s)
Prevention

P210 Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking.

P233 Keep container tightly closed.

P240 Ground and bond container and receiving equipment.

P241 Use explosion-proof [electrical/ventilating/lighting/...] equipment.

P242 Use non-sparking tools.

P243 Take action to prevent static discharges.

P280 Wear protective gloves/protective clothing/eye protection/face protection.

P264 Wash ... thoroughly after handling.

P261 Avoid breathing dust/fume/gas/mist/vapours/spray.

P271 Use only outdoors or in a well-ventilated area.

Response

P303+P361+P353 IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water [or shower].

P370+P378 In case of fire: Use ... to extinguish.

P302+P352 IF ON SKIN: Wash with plenty of water/...

P321 Specific treatment (see ... on this label).

P332+P313 If skin irritation occurs: Get medical advice/attention.

P362+P364 Take off contaminated clothing and wash it before reuse.

P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.

P337+P313 If eye irritation persists: Get medical advice/attention.

P304+P340 IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P312 Call a POISON CENTER/doctor/\u2026if you feel unwell.

Storage

P403+P235 Store in a well-ventilated place. Keep cool.

P403+P233 Store in a well-ventilated place. Keep container tightly closed.

P405 Store locked up.

Disposal

P501 Dispose of contents/container to ...

2.3 Other hazards which do not result in classification

none

6. NMR Spectrum
13C NMR : in CDCl3  
1H NMR : parameter in CDCl3  
IR : CCl4 solution  
IR : liquid film  
Raman : 4880 A,200 M,liquid  
Mass  
7. Synthesis Route
77-76-9Total: 33 Synthesis Route
 
58-56-0
58-56-0 268 Suppliers
 
 
77-76-9
77-76-9 170 Suppliers
   
77-76-9
77-76-9 170 Suppliers
8. Precursor and Product
precursor:
product:
9. Computed Properties
10.Other Information
Usage
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.
BRN
635678
Chemical Properties
colourless liquid
Uses
2,2-Dimethoxypropane(DMP) is used in histology and considered to be more efficient than ethanol for the dehydration of animal tissue.
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.
Mesh Entry Terms
2,2-dimethoxypropane
Manufacturing Info
Propane, 2,2-dimethoxy-: ACTIVE
11. Toltal 158 Suppliers View more
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12. Related Questions
What are the applications of 2,2-Dimethoxypropane?2,2-Dimethoxypropane has various applications in the preparation of acetal, acetone compounds, isopropyl derivatives, amino acid esters, and enol ethers. It is also used in the synthesis of phosphate ..
Introduction of 2,2-DimethoxypropaneFormation of Acetals. The reagent can be used to prepare a variety of acetals via transacetalization. This involves interchanging the alkoxy or ketone groups in an acidic medium. Both symmetrical [R1R..
What is 2,2-Dimethoxypropane and its Applications? 【中文名称】 2,2-Dimethoxypropane 【英文名称】2,2-Dimethoxypropane 【分子式】C5H12O2 【分子量】104.15 【CAS登录号】[77-76-9] 【缩写和别名】Acetone Dimethyl Acetal 【结构式】 【物理性质】2,2-Dimethoxy..
13. Realated Product Infomation
 
 
 
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