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Sigma-Aldrich

2,6-Bis(hydroxymethyl)-p-cresol

95%

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Linear Formula:
CH3C6H2(CH2OH)2OH
CAS Number:
Molecular Weight:
168.19
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

vapor density

5.8 (vs air)

Quality Level

Assay

95%

impurities

<3% sodium hydroxide

mp

128-130 °C (lit.)

SMILES string

Cc1cc(CO)c(O)c(CO)c1

InChI

1S/C9H12O3/c1-6-2-7(4-10)9(12)8(3-6)5-11/h2-3,10-12H,4-5H2,1H3

InChI key

KUMMBDBTERQYCG-UHFFFAOYSA-N

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1 of 4

This Item
D4879649546554693
(2-Hydroxyethyl)urea 95%

Sigma-Aldrich

554693

(2-Hydroxyethyl)urea

mp

128-130 °C (lit.)

mp

125 °C (dec.) (lit.)

mp

183-187 °C (lit.)

mp

164-169 °C (lit.)

vapor density

5.8 (vs air)

vapor density

-

vapor density

-

vapor density

-

impurities

<3% sodium hydroxide

impurities

-

impurities

-

impurities

-

Application

2,6-Bis(hydroxymethyl)-p-cresol was used as a bridging ligand in binuclear oxovanadium(V) compound, which on exposure to white light and aerial oxygen forms an oligomeric compound.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Customers Also Viewed

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Zehong Xiang et al.
Biomaterials science, 8(21), 6025-6036 (2020-10-01)
Thrombotic and inflammatory complications induced by vascular implants remain a challenge to treat cardiovascular disease due to the lack of self-adaption and functional integrity of implants. Inspired by the dynamic remodeling of the extracellular matrix (ECM), we constructed a bio-mimic
Pabitra Baran Chatterjee et al.
Journal of the American Chemical Society, 132(45), 15842-15845 (2010-10-23)
An unprecedented single crystal-to-single crystal transformation occurs when a binuclear oxovanadium(V) compound [V(V)(2)O(2)(L)(2)] 1 involving 2,6-bis(hydroxymethyl)-p-cresol (H(3)L) as a bridging ligand is exposed simultaneously to white light and aerial oxygen to generate an oligomeric compound [V(IV)(2)O(2)(L*)(2)] 2 (H(2)L* is 3-hydroxymethyl-5-methylsalicylaldehyde).
Youngkeun Lee et al.
The Analyst, 143(8), 1780-1785 (2018-01-31)
The development of artificial peroxidases has attracted great interest because of their applications in various fields such as the chemical industry and biosensing. In this study, 2,6-bis[(bis(2-pyridylmethyl)amino)-methyl]-4-methylphenol (H-bpmp) complexes with various transition metal ions have been investigated as artificial peroxidases.

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