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448958

Sigma-Aldrich

Thymine-1-acetic acid

98%

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About This Item

Empirical Formula (Hill Notation):
C7H8N2O4
CAS Number:
20924-05-4
Molecular Weight:
184.15
MDL number:
MFCD00274250
UNSPSC Code:
12352100
PubChem Substance ID:
24868444
NACRES:
NA.22

assay

98%

form

solid

mp

272-278 °C (dec.) (lit.)

SMILES string

CC1=CN(CC(O)=O)C(=O)NC1=O

InChI

1S/C7H8N2O4/c1-4-2-9(3-5(10)11)7(13)8-6(4)12/h2H,3H2,1H3,(H,10,11)(H,8,12,13)

InChI key

TZDMCKHDYUDRMB-UHFFFAOYSA-N

Related Categories

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Giant vesicle formation through self-assembly of complementary random copolymers.
Ilhan F, et al.
Journal of the American Chemical Society, 122(24), 5895-5896 (2000)
Ojodomo J Achadu et al.
Mikrochimica acta, 185(10), 461-461 (2018-09-17)
A microwave-assisted hydrothermal method was employed to prepare thymine-modified graphitic carbon nitride quantum dots (T-gCNQDs) which are shown to be a novel fluorescent nanoprobe for Hg(II). They exhibit excellent optical properties (blue emission with a fluorescence quantum yield of 46%)
Pilar Amo-Ochoa et al.
Inorganic chemistry, 52(19), 11428-11437 (2013-09-18)
Four new copper(II) coordination complexes, obtained by reaction of CuX2 (X = acetate or chloride) with thymine-1-acetic acid and uracil-1-propionic acid as ligands, of formulas [Cu(TAcO)2(H2O)4]·4H2O (1), [Cu(TAcO)2(H2O)2]n (2), [Cu3(TAcO)4(H2O)2(OH)2]n·4H2O (3), and [Cu3(UPrO)2Cl2(OH)2(H2O)2]n (4) (TAcOH = thymine-1-acetic acid, UPrOH =
Nan Wang et al.
Biosensors & bioelectronics, 79, 320-326 (2016-01-01)
A sensitive, selective and reusable electrochemical biosensor for the determination of mercury ions (Hg(2+)) has been developed based on thymine (T) modified gold nanoparticles/reduced graphene oxide (AuNPs/rGO) nanocomposites. Graphene oxide (GO) was electrochemically reduced on a glassy carbon substrate. Subsequently
P J Finn et al.
Nucleic acids research, 24(17), 3357-3363 (1996-09-01)
Adenine, thymine and cytosine PNA monomers have been prepared using 3-amino-1,2-propanediol as a starting material. The benzoyl group was used to protect the exocyclic amines of the heterocyclic bases of A and C PNA monomers and the backbone primary amine
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