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[ CAS No. 1002-67-1 ]

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Cat. No.: {[proInfo.prAm]}
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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
Excepted Quantity Free
Inaccessible (Haz class 6.1), Domestic USD 41.00
Inaccessible (Haz class 6.1), International USD 64.00
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 83.00
Accessible (Haz class 3, 4, 5 or 8), International USD 133.00
Chemical Structure| 1002-67-1
Chemical Structure| 1002-67-1
Structure of 1002-67-1 * Storage: {[proInfo.prStorage]}

Quality Control of [ 1002-67-1 ]

Related Doc. of [ 1002-67-1 ]

SDS
Alternatived Products of [ 1002-67-1 ]
Alternatived Products of [ 1002-67-1 ]

Product Details of [ 1002-67-1 ]

CAS No. :1002-67-1 MDL No. :MFCD01727263
Formula : C7H16O3 Boiling Point : 167.9°C at 760 mmHg
Linear Structure Formula :- InChI Key :N/A
M.W :148.20 g/mol Pubchem ID :-
Synonyms :

Safety of [ 1002-67-1 ]

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:
GHS Pictogram:

Application In Synthesis of [ 1002-67-1 ]

  • Downstream synthetic route of [ 1002-67-1 ]

[ 1002-67-1 ] Synthesis Path-Downstream   1~16

YieldReaction ConditionsOperation in experiment
With nickel at 170 - 210℃; Hydrogenation.unter Druck;
  • 2
  • [ 66854-10-2 ]
  • [ 111-77-3 ]
  • [ 1002-67-1 ]
YieldReaction ConditionsOperation in experiment
at 170 - 210℃; Hydrogenation;
YieldReaction ConditionsOperation 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.
YieldReaction ConditionsOperation 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.
YieldReaction ConditionsOperation 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.
  • 6
  • [ 1002-67-1 ]
  • C13H20O5 [ No CAS ]
  • [ 1254055-77-0 ]
YieldReaction ConditionsOperation in experiment
55% In chloroform at 20℃; for 48h; Molecular sieve; Inert atmosphere;
  • 7
  • [ 1002-67-1 ]
  • C15H24O5 [ No CAS ]
  • [ 1254055-79-2 ]
YieldReaction ConditionsOperation in experiment
86% In chloroform at 20℃; for 48h; Molecular sieve; Inert atmosphere;
  • 8
  • [ 1002-67-1 ]
  • 2,5-dioxotetrahydrofuran-3-yl n-dodecanoate [ No CAS ]
  • [ 1254055-63-4 ]
YieldReaction ConditionsOperation in experiment
89% In chloroform at 20℃; for 48h; Molecular sieve; Inert atmosphere;
  • 9
  • [ 1002-67-1 ]
  • C19H32O5 [ No CAS ]
  • [ 1254055-80-5 ]
YieldReaction ConditionsOperation in experiment
88% In chloroform at 20℃; for 48h; Molecular sieve; Inert atmosphere;
  • 10
  • [ 1002-67-1 ]
  • C21H36O5 [ No CAS ]
  • [ 1254055-81-6 ]
YieldReaction ConditionsOperation in experiment
95% In chloroform at 20℃; for 48h; Molecular sieve; Inert atmosphere;
  • 11
  • [ 1002-67-1 ]
  • C23H40O5 [ No CAS ]
  • [ 1254055-83-8 ]
YieldReaction ConditionsOperation in experiment
91% In chloroform at 60℃; for 48h; Molecular sieve; Inert atmosphere;
  • 12
  • [ 1002-67-1 ]
  • C20H36O5 [ No CAS ]
  • [ 1254055-93-0 ]
YieldReaction ConditionsOperation in experiment
59% In chloroform at 60℃; for 48h; Molecular sieve; Inert atmosphere;
  • 13
  • [ 1002-67-1 ]
  • C24H44O5 [ No CAS ]
  • [ 1254055-95-2 ]
YieldReaction ConditionsOperation in experiment
84% In chloroform at 60℃; for 48h; Molecular sieve; Inert atmosphere;
  • 14
  • [ 1002-67-1 ]
  • C32H60O5 [ No CAS ]
  • [ 1254055-97-4 ]
YieldReaction ConditionsOperation in experiment
83% In chloroform at 60℃; for 48h; Molecular sieve; Inert atmosphere;
  • 15
  • [ 1002-67-1 ]
  • C36H68O5 [ No CAS ]
  • [ 1254055-99-6 ]
YieldReaction ConditionsOperation in experiment
96% In chloroform at 60℃; for 48h; Molecular sieve; Inert atmosphere;
  • 16
  • [ 1002-67-1 ]
  • C40H76O5 [ No CAS ]
  • [ 1254056-01-3 ]
YieldReaction ConditionsOperation in experiment
92% In chloroform at 60℃; for 48h; Molecular sieve; Inert atmosphere;
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