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T1375

Sigma-Aldrich

TES

≥99% (titration)

Synonym(s):

2-[(2-Hydroxy-1,1-bis(hydroxymethyl)ethyl)amino]ethanesulfonic acid, N-[Tris(hydroxymethyl)methyl]-2-aminoethanesulfonic acid, TES free acid

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About This Item

Empirical Formula (Hill Notation):
C6H15NO6S
CAS Number:
7365-44-8
Molecular Weight:
229.25
Beilstein:
1957061
EC Number:
230-906-3
MDL number:
MFCD00007532
UNSPSC Code:
12161700
PubChem Substance ID:
24899960
NACRES:
NA.25

Quality Level

200

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Palmelloids formation in Chlamydomonas reinhardtii: defence against rotifer predators?
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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
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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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Protocols

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This procedure may be used for Mutanolysin products.

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