Home Cart Sign in  
HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 122-31-6 Chemical Structure| 122-31-6
Chemical Structure| 122-31-6

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of 1,1,3,3-Tetraethoxypropane

CAS No. :122-31-6
Formula : C11H24O4
M.W : 220.31
SMILES Code : CCOC(OCC)CC(OCC)OCC
MDL No. :MFCD00009240
InChI Key :KVJHGPAAOUGYJX-UHFFFAOYSA-N
Pubchem ID :67147

Safety of 1,1,3,3-Tetraethoxypropane

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H225-H302
Precautionary Statements:P210-P233-P240-P241-P242-P243-P264-P270-P280-P301+P312+P330-P303+P361+P353-P370+P378-P403+P235-P501
Class:3
UN#:3271
Packing Group:

Application In Synthesis of 1,1,3,3-Tetraethoxypropane

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 122-31-6 ]

[ 122-31-6 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 122-31-6 ]
  • [ 33906-30-8 ]
  • [ 55317-53-8 ]
  • 2
  • [ 122-31-6 ]
  • [ 1450-93-7 ]
  • [ 274-95-3 ]
  • 3
  • [ 122-31-6 ]
  • [ 658-27-5 ]
  • 1-(3-fluorophenyl)-1H-pyrazole [ No CAS ]
  • 4
  • [ 122-31-6 ]
  • [ 504-02-9 ]
  • [ 53400-41-2 ]
YieldReaction ConditionsOperation in experiment
With ammonium acetate; In xylene; at 160℃; for 18h; In a nitrogen atmosphere, 24 mL of malonaldehyde tetraethyl acetal and 7.71 g of ammonium acetate were added in that order to xylene (80 mL) solution of 11.2 g of 1,3-cyclohexadione, and a reflux condenser tube fitted with a Dean-Stark water separator was attached to the reactor, and this was stirred at 160C for 18 hours. The reaction liquid was cooled to room temperature, the solvent was evaporated off under reduced pressure, the residue was extracted with chloroform, and the chloroform layer was washed with saturated saline water and dried with anhydrous sodium sulfate. The solvent was evaporated off under reduced pressure, and the residue was separated and purified through silica gel column chromatography (chloroform/methanol = 97/3) to obtain 2.21 g of the entitled compound.
  • 5
  • [ 122-31-6 ]
  • [ 5220-49-5 ]
  • [ 53400-41-2 ]
YieldReaction ConditionsOperation in experiment
7% toluene-4-sulfonic acid; In N,N-dimethyl-formamide; for 16h;Heating / reflux; A mixture of 3-aminocyclohex-2-enone (100 mmol), 1 ,1 , 3,3- tetraethoxypropane (1 10 mmol), and 4-methylbenzenesulfonic acid (2.91 mmol) is diluted with lambda/,lambda/-dimethylformamide (40 ml_) and the reaction mixture is heated at reflux for 16 h. The reaction mixture is allowed to cool to rt, neutralized with sodium bicarbonate, diluted with water (400 ml_), and is extracted with ethyl acetate (3 x 100 ml_). The combined organic layers are dried (sodium sulfate) and concentrated. The residue is purified by chromatography (10/1 petroleum ether/ethyl acetate) to provide 5,6,7,8-tetrahydroquinolin-5-one in 7% yield as a colorless oil.
toluene-4-sulfonic acid; In N,N-dimethyl-formamide; at 140℃; for 18h; To a solution of 10.12 g (0.14 mmol) 3-aminocyclohex-2-en-l-one and 22 mL 1,1,3,3- tetraethoxypropane in 40 mL dry DMF under nitrogen atmosphere was added 0.5 g (cat.) p- toluenesulfonic acid. The reaction mixture was heated at 140 0C for 18 hr. The volatiles were removed under vacuum and the residue distilled under vacuum to give an oil. This material was further purified by column chromatography on silica gel eluting with hexanes/EtOAc (3/1) then EtOAc (100%) afford 1.75 g of the title compound. LC-MS: (MH)+: 148.2.
 

Historical Records

Technical Information

Categories