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670189

Sigma-Aldrich

Cholin acetate

≥95.0% (T)

Synonym(s):

2-Hydroxyethyl-trimethylammonium acetate, COL Acetate

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5 G
$169.00
50 G
$763.00

About This Item

Empirical Formula (Hill Notation):
C7H17NO3
CAS Number:
14586-35-7
Molecular Weight:
163.21
MDL number:
MFCD29072955
UNSPSC Code:
12352100
PubChem Substance ID:
24885068
NACRES:
NA.22

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Quality Level

100

assay

≥95.0% (T)

form

solid

impurities

≤1.0% water

functional group

amine
hydroxyl

SMILES string

CC([O-])=O.C[N+](C)(C)CCO

InChI

1S/C5H14NO.C2H4O2/c1-6(2,3)4-5-7;1-2(3)4/h7H,4-5H2,1-3H3;1H3,(H,3,4)/q+1;/p-1

Inchi Key

QLKGUVGAXDXFFW-UHFFFAOYSA-M

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General description

Cholin acetate is a choline-derivative-based ionic liquid (IL), which can efficiently dissolve microcrystalline cellulose.[1] This bioionic liquid can be prepared by reacting choline hydroxide with acetic acid.[2]

Application

Cholin acetate in combination with glycerol, a hydrogen-bond donor forms a eutectic ionic liquid mixture, which is less viscous, biodegradable and also shows high lipase compatibility. This eutectic ionic liquid mixture can be a desirable solvent for the enzymatic production of biodiesel.[3]

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

284.0 °F - closed cup

flash_point_c

140.00 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM7733
BCCL4030
BCCH5331
BCCH4157
BCCJ4614

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Bio ionic liquids: room temperature ionic liquids composed wholly of biomaterials.
Fukaya Y, et al.
Green Chemistry, 9(11), 1155-1157 (2007)
Low melting mixtures in organic synthesis-an alternative to ionic liquids?.
Ru? C and Konig B.
Green Chemistry, 14(11), 2969-2982 (2012)
Hua Zhao et al.
Organic & biomolecular chemistry, 9(6), 1908-1916 (2011-02-02)
The enzymatic preparation of biodiesel has been hampered by the lack of suitable solvents with desirable properties such as high lipase compatibility, low cost, low viscosity, high biodegradability, and ease of product separation. Recent interest in using ionic liquids (ILs)

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