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+ |
Purity | Size | Price | VIP Price | USA Stock *0-1 Day | Global Stock *5-7 Days | Quantity | |||||
{[ item.p_purity ]} | {[ item.pr_size ]} |
{[ getRatePrice(item.pr_usd, 1,1) ]} {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate) ]} |
{[ getRatePrice(item.pr_usd, 1,1) ]} | {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate) ]} {[ getRatePrice(item.pr_usd,1,item.mem_rate) ]} | {[ item.pr_usastock ]} | Inquiry - | {[ item.pr_chinastock ]} | Inquiry - |
* Storage: {[proInfo.prStorage]}
CAS No. : | 1002-67-1 | MDL No. : | MFCD01727263 |
Formula : | C7H16O3 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | CNJRPYFBORAQAU-UHFFFAOYSA-N |
M.W : | 148.20 g/mol | Pubchem ID : | 13847 |
Synonyms : |
|
Signal Word: | Danger | Class: | 3 |
Precautionary Statements: | P501-P240-P210-P233-P243-P241-P242-P280-P370+P378-P303+P361+P353-P403+P235 | UN#: | 3271 |
Hazard Statements: | H225 | Packing Group: | Ⅲ |
GHS Pictogram: |
![]() |
* 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.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With nickel at 170 - 210℃; Hydrogenation.unter Druck; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
at 170 - 210℃; Hydrogenation; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With barium dihydroxide; carbon dioxide In mineral spirits at 140℃; for 1 - 1.5h; | 7 A one-liter resin kettle, equipped with a mechanical stirrer, distillation condenser and a thermometer, was charged with 160 g of mineral spirits, 83 g of 2-ethyl hexanoic acid, 70 g of triethylene glycol, 70 g of methyl carbitol and 331 g of barium hydroxide monohydrate. The reactor contents were then heated slowly to 140C, and water was removed. Carbon dioxide was then turned on at a rate of 1 LPM (liter per minute) for 1 to 1.5 hours, and water of the reaction was removed. The product was filtered using a filter aid at 140C and a very light colored liquid product containing 31% barium was obtained. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With barium dihydroxide; carbon dioxide In mineral spirits at 140℃; for 1 - 1.5h; | 1 A one-liter resin kettle, equipped with a mechanical stirrer, distillation condenser and a thermometer, was charged with 173 g of mineral spirits, 83 g of 2-ethyl hexanoic acid, 34 g of oleyl alcohol, 21 g of methyl carbitol and 331 g of barium hydroxide monohydrate. The reactor contents were then heated slowly to 140C, and water was removed. Carbon dioxide was then turned on at a rate of 1 LPM (liter per minute) for 1 to 1.5 hours, and water of the reaction was removed. Mineral spirits was then replaced with a mineral oil. The product was filtered using a filter aid at 140C and a very light colored liquid product containing 40% barium was obtained. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With barium dihydroxide; carbon dioxide In mineral spirits at 140℃; for 1 - 1.5h; | 4 A one-liter resin kettle, equipped with a mechanical stirrer, distillation condenser and a thermometer, was charged with 160 g of mineral spirits, 83 G OF 2-ethyl hexanoic acid, 70 g of a glycol ester of a fatty acid, 70 g of methyl carbitol and 331 g of barium hydroxide monohydrate. The reactor contents were then heated slowly to 140C, and water was removed. Carbon dioxide was then turned on at a rate of 1 LPM (liter per minute) for 1 to 1.5 hours, and water of the reaction was removed. The product was filtered using a filter aid at 140C and a very light colored liquid product containing 36% barium was obtained. | |
With barium dihydroxide; carbon dioxide In mineral spirits at 140℃; for 1 - 1.5h; | 6 A one-liter resin kettle, equipped with a mechanical stirrer, distillation condenser and a thermometer, was charged with 160 g of mineral spirits, 83 g of 2-ethyl hexanoic acid, 70 g of dipropylene glycol methyl ether, 70 g of methyl carbitol and 331 g of barium hydroxide monohydrate. The reactor contents were then heated slowly to 140C, and water was removed. Carbon dioxide was then turned on at a rate of 1 LPM (liter per minute) for 1 to 1.5 hours, and water of the reaction was removed. The product was filtered using a filter aid at 140C and a very light colored liquid product containing 34% barium was obtained. | |
With barium dihydroxide; carbon dioxide In mineral spirits at 140℃; for 1 - 1.5h; | 5 A one-liter resin kettle, equipped with a mechanical stirrer, distillation condenser and a thermometer, was charged with 160 g of mineral spirits, 83 g of 2-ethyl hexanoic acid, 70 g of propylene glycol butyl ether, 70 g of methyl carbitol and 331 g of barium hydroxide monohydrate. The reactor contents were then heated slowly to 140C, and water was removed. Carbon dioxide was then turned on at a rate of 1 LPM (liter per minute) for 1 to 1.5 hours, and water of the reaction was removed. The product was filtered using a filter aid at 140C and a very light colored liquid product containing 37% barium was obtained. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
55% | In chloroform at 20℃; for 48h; Molecular sieve; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
86% | In chloroform at 20℃; for 48h; Molecular sieve; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
89% | In chloroform at 20℃; for 48h; Molecular sieve; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
88% | In chloroform at 20℃; for 48h; Molecular sieve; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
95% | In chloroform at 20℃; for 48h; Molecular sieve; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
91% | In chloroform at 60℃; for 48h; Molecular sieve; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
59% | In chloroform at 60℃; for 48h; Molecular sieve; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
84% | In chloroform at 60℃; for 48h; Molecular sieve; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
83% | In chloroform at 60℃; for 48h; Molecular sieve; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
96% | In chloroform at 60℃; for 48h; Molecular sieve; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
92% | In chloroform at 60℃; for 48h; Molecular sieve; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
85% | In chloroform for 48h; Molecular sieve; Inert atmosphere; Reflux; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With H-type ZSM-5(SiO2/Al2O3=280) at 180℃; for 8h; | 7 5 parts of H-type ZSM-5 (SiO2 / Al2O3 = 280), 50 parts of diethylene glycol monomethyl ether, and diethylene glycol monoethyl ether 50 parts were charged into a reaction vessel and heated up to 180 ° C. under stirring for 8 hours It stirred. After cooling to room temperature, the reaction solution was measured the relative amounts of products were analyzed by gas chromatography. The composition of the resulting diethylene glycol ethyl methyl ether was 7.7%. Further, resulting in the product, diethylene glycol dimethyl ether and diethylene glycol diethyl ether, were contained in 3.7% and 5.2% of the composition ratio, respectively as by-products. By the diethylene glycol dimethyl ether exchange reaction together diethylene glycol monomethyl ether of the raw material, the diethylene glycol diethyl ether by ether exchange reaction together diethylene glycol monoethyl ether starting material, believed to be respectively obtained |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
1: 26 %Spectr. 2: 23 %Spectr. | In benzene-d6 at 80℃; for 24h; |
[ 112-60-7 ]
2,2'-((Oxybis(ethane-2,1-diyl))bis(oxy))diethanol
Similarity: 1.00
[ 112-35-6 ]
2-(2-(2-Methoxyethoxy)ethoxy)ethanol
Similarity: 1.00
[ 6809-70-7 ]
3,6,9,12,15,18,21,24,27,30-Decaoxadotriacontane-1,32-diol
Similarity: 1.00
[ 112-60-7 ]
2,2'-((Oxybis(ethane-2,1-diyl))bis(oxy))diethanol
Similarity: 1.00
[ 112-35-6 ]
2-(2-(2-Methoxyethoxy)ethoxy)ethanol
Similarity: 1.00
[ 6809-70-7 ]
3,6,9,12,15,18,21,24,27,30-Decaoxadotriacontane-1,32-diol
Similarity: 1.00