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T1375

Sigma-Aldrich

TES

≥99% (titration)

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Synonym(s):
2-[(2-Hydroxy-1,1-bis(hydroxymethyl)ethyl)amino]ethanesulfonic acid, N-[Tris(hydroxymethyl)methyl]-2-aminoethanesulfonic acid, TES free acid
Empirical Formula (Hill Notation):
C6H15NO6S
CAS Number:
Molecular Weight:
229.25
Beilstein:
1957061
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.25

Quality Level

Assay

≥99% (titration)

form

crystalline powder

useful pH range

6.8-8.2

pKa (25 °C)

7.5

mp

~225 °C (dec.)

solubility

H2O: 25 g plus 50 mL, clear, colorless

application(s)

diagnostic assay manufacturing

SMILES string

OCC(CO)(CO)NCCS(O)(=O)=O

InChI

1S/C6H15NO6S/c8-3-6(4-9,5-10)7-1-2-14(11,12)13/h7-10H,1-5H2,(H,11,12,13)

InChI key

JOCBASBOOFNAJA-UHFFFAOYSA-N

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Application

TES has been used in TES buffer to determine anti-collagenase activity of Marula stems. It has also been used in buffers for cell culture medium.

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Palmelloids formation in Chlamydomonas reinhardtii: defence against rotifer predators?
Lurling M and Beekman W
Annales de Limnologie-International Journal of Limnology, 42(2), 65-72 (2006)
Anti-aging potential of extracts from Sclerocarya birrea (A. Rich.) Hochst and its chemical profiling by UPLC-Q-TOF-MS
Shoko T, et al.
BMC Complementary and Alternative Medicine, 18(1), 54-54 (2018)
Isolation of Tomato Fruit Chromoplasts and Determination of ATP Levels
Hernandez-Gras F, et al.
The Plant Journal, 18(1), 54-54 (2013)
Carmen Hierro-Bujalance et al.
Frontiers in cell and developmental biology, 8, 571258-571258 (2020-10-13)
The germinal matrix-intraventricular hemorrhage (GM-IVH) is one of the most devastating complications of prematurity. The short- and long-term neurodevelopmental consequences after severe GM-IVH are a major concern for neonatologists. These kids are at high risk of psychomotor alterations and cerebral
Yikang Wu et al.
Organic letters, 4(13), 2141-2144 (2002-06-21)
[reaction: see text] In DMSO cleavage of triethylsilyl (TES) ethers by o-iodoxybenzoic acid (IBX) was significantly faster than cleavage of tert-butyldimethylsilyl (TBS) ethers or further oxidation into carbonyl compounds. In most cases, TES protecting groups could be removed in good

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