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Sigma-Aldrich

Tris(2-carboxyéthyl)phosphine hydrochloride

BioUltra, ≥98% (NMR)

Synonyme(s) :

TCEP

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About This Item

Formule empirique (notation de Hill):
C9H15O6P · HCl
Numéro CAS:
51805-45-9
Poids moléculaire :
286.65
Numéro Beilstein :
3724376
Numéro MDL:
MFCD00145469
Code UNSPSC :
12352128
ID de substance PubChem :
329766294
Nomenclature NACRES :
NA.25

Gamme de produits

BioUltra

Pureté

≥98% (NMR)

Forme

crystals

Pertinence de la réaction

reagent type: reductant

Perte

≤1.0% loss on drying

pH

1.2-1.5

Solubilité

H2O: 1 M, clear, colorless (no residue)

Traces d'anions

sulfate (SO42-): ≤50 mg/kg

Traces de cations

Al: ≤5 mg/kg
As: ≤0.05 mg/kg
Ba: ≤5 mg/kg
Bi: ≤5 mg/kg
Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤50 mg/kg
Li: ≤5 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Mo: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Sr: ≤5 mg/kg
Zn: ≤5 mg/kg

λ

0.1 M in H2O

Absorption UV

λ: 260 nm Amax: 0.05
λ: 280 nm Amax: 0.03

Température de stockage

2-8°C

Chaîne SMILES 

Cl[H].OC(=O)CCP(CCC(O)=O)CCC(O)=O

InChI

1S/C9H15O6P.ClH/c10-7(11)1-4-16(5-2-8(12)13)6-3-9(14)15;/h1-6H2,(H,10,11)(H,12,13)(H,14,15);1H

Clé InChI

PBVAJRFEEOIAGW-UHFFFAOYSA-N

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Description générale

Tris(2-carboxyethyl)-phosphine hydrochloride (TCEP) is a strong reducing agent that is stable in an aqueous solution. It readily and stoichiometrically reduces disulfides with high specificity. TCEP exhibits reducing activity at pH 1.5 to pH 9.0 and reduces dehydroascorbic acid (DHA) at pH 4.

Application

Tris(2-carboxyethyl)phosphine hydrochloride has been used:
  • as a component of IRE1 dialysis buffer, RNA cleavage buffer, and in in vitro cleavage assay of in vitro transcribed RNA
  • in reducing sulfhydryl groups to obtain total thiol fraction
  • to reduce protein samples

Water soluble reagent, used for selective reduction of disulfides. More stable than DTT and useful in mass spectrometry applications.

Pictogrammes

Corrosion
GHS05

Mention d'avertissement

Danger

Mentions de danger

H314

Classification des risques

Eye Dam. 1 - Skin Corr. 1B

Code de la classe de stockage

8A - Combustible corrosive hazardous materials

Classe de danger pour l'eau (WGK)

WGK 1

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Consulter la Bibliothèque de documents

G Elif Karagöz et al.
Bio-protocol, 9(14), e3307-e3307 (2019-07-20)
The kinase/RNase IRE1 is a key effector of the cellular response to endoplasmic reticulum stress. The RNase activity of IRE1 can be measured in cells or in the test tube. Here we describe a protocol for the in vitro cleavage
Yasunori Sato et al.
Biological & pharmaceutical bulletin, 33(3), 364-369 (2010-03-02)
Ascorbic acid (AA) has a strong anti-oxidant function evident as its ability to scavenge superoxide radicals in vitro. Moreover, AA is an essential ingredient for post-translational proline hydroxylation of collagen molecules. Dehydroascorbic acid (DHA), the oxidized form of AA, is
Lena Munzel et al.
Autophagy, 17(6), 1458-1478 (2020-06-10)
Coupling of Atg8 to phosphatidylethanolamine is crucial for the expansion of the crescent-shaped phagophore during cargo engulfment. Atg21, a PtdIns3P-binding beta-propeller protein, scaffolds Atg8 and its E3-like complex Atg12-Atg5-Atg16 during lipidation. The crystal structure of Atg21, in complex with the
Maria João Correia et al.
Antioxidants (Basel, Switzerland), 10(9) (2021-09-29)
We hypothesized that an interplay between aryl hydrocarbon receptor (AhR) and cysteine-related thiolome at the kidney cortex underlies the mechanisms of (mal)adaptation to chronic intermittent hypoxia (CIH), promoting arterial hypertension (HTN). Using a rat model of CIH-HTN, we investigated the
Lucas B Harrington et al.
Molecular cell, 79(3), 416-424 (2020-07-10)
CRISPR-Cas12c/d proteins share limited homology with Cas12a and Cas9 bacterial CRISPR RNA (crRNA)-guided nucleases used widely for genome editing and DNA detection. However, Cas12c (C2c3)- and Cas12d (CasY)-catalyzed DNA cleavage and genome editing activities have not been directly observed. We
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