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Tetraglycol - BioReagent Plus, high purity , CAS No.31692-85-0

2 Citations

COA

Grade & Purity:

UltraBio™

Ultra pure

Cas Number: 31692-85-0
PubChem CID: 110717

In stock

Item Number

T432615

Grouped product items
SKU	Size	Availability	Price	Qty
T432615-25g	25g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$49.90
T432615-100g	100g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$129.90

View related series

Biochemical Assay Reagents (928) Solubilizer (11)

Basic Description

Synonyms	Glycofurol \| Tetrahydrofurfuryl polyethylene glycol ether \| Tetrahydrofurfuryl alcohol polyethyleneglycol ethe
Specifications & Purity	UltraBio™, Ultra pure
Biochemical and Physiological Mechanisms	Liquid glycofurol can readily transform into gel systems with excellent elasticity due to which, it can be used as a medium to dissolve water-insoluble drugs.
Grade	Ultra pure, UltraBio™
Note	注意: 请勿与三缩四乙二醇混淆，其有时也称为四甘醇。
Product Description	Efficient solubilizer for glibenclamide (GBD)

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Tetrahydrofurans

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Tetrahydrofurans
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Tetrahydrofurans
Alternative Parents	Oxacyclic compounds Dialkyl ethers Primary alcohols Hydrocarbon derivatives
Molecular Framework	Aliphatic heteromonocyclic compounds
Substituents	Tetrahydrofuran - Oxacycle - Ether - Dialkyl ether - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as tetrahydrofurans. These are heterocyclic compounds containing a saturated, aliphatic, five-membered ring where a carbon is replaced by an oxygen.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

IUPAC Name	2-(oxolan-2-ylmethoxy)ethanol
INCHI	InChI=1S/C7H14O3/c8-3-5-9-6-7-2-1-4-10-7/h7-8H,1-6H2
InChIKey	CTPDSKVQLSDPLC-UHFFFAOYSA-N
Smiles	C1CC(OC1)COCCO
Isomeric SMILES	C1CC(OC1)COCCO
WGK Germany	3
RTECS	MD0907500

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

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4 results found

Lot Number	Certificate Type	Date	Item
H2409669	Certificate of Analysis	Jul 30, 2024	T432615
H2409670	Certificate of Analysis	Jul 30, 2024	T432615
H2409671	Certificate of Analysis	Jul 30, 2024	T432615
H2409672	Certificate of Analysis	Jul 30, 2024	T432615

Chemical and Physical Properties

Refractive Index	1.462
Specific Rotation[α]	+0.4°（C=0.5，methanol）
Flash Point(°F)	275.0 °F
Flash Point(°C)	135 °C
Melt Point(°C)	≤ -100 °C
Molecular Weight	146.180 g/mol
XLogP3	-0.200
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	4
Exact Mass	146.094 Da
Monoisotopic Mass	146.094 Da
Topological Polar Surface Area	38.700 Å²
Heavy Atom Count	10
Formal Charge	0
Complexity	84.900
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	1
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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