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Tris(2-carboxyethyl)phosphine hydrochloride solution_Molecular_structure_CAS_51805-45-9)
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Tris(2-carboxyethyl)phosphine hydrochloride solution

Catalog No. 646547 Name Sigma Aldrich
CAS Number 51805-45-9 Website http://www.sigmaaldrich.com
M. F. C9H16ClO6P Telephone 1-800-521-8956
M. W. 286.646501 Fax
Purity Email
Storage Chembase ID: 144570

SYNONYMS

Title
三(2-羧乙基)膦 盐酸盐 溶液
IUPAC name
3-[bis(2-carboxyethyl)phosphanyl]propanoic acid hydrochloride
IUPAC Traditional name
tris(2-carboxyethyl)phosphine hydrochloride
Synonyms
TCEP

DATABASE IDS

MDL Number MFCD00145469
PubChem SID 24883469
CAS Number 51805-45-9

PROPERTIES

Concentration 0.5 M
Empirical Formula (Hill Notation) C9H15O6P · HCl
Density 1.041 g/mL at 25 °C
pH 7.0
Refractive Index n20/D 1.367
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Precautionary statements P305 + P351 + P338
Risk Statements 36
Safety Statements 26
German water hazard class 2

DETAILS

Description (English)
Packaging
1, 10×1 mL in ampule
Application
TCEP is an effective reducing agent for protein analysis. As a non-mercaptan reducing agent, it avoids the toxicity inherent in thiol-containing compounds. It is capable of disrupting the botulinum neurotoxin B heavy-chain/light-chain complex that is held together by a single disulfide bond, and that is responsible for endocytosis, and ultimately the toxicity, of the toxin. Since disulfide-coupled subunits are characteristic of many toxins (e.g., ricin, snake venom, and all BoNT serotypes), it may be useful as a rescue prophylactic in cases of toxin administration.1
Description (简体中文)
包装
1, 10×1 mL in ampule
Application
TCEP is an effective reducing agent for protein analysis. As a non-mercaptan reducing agent, it avoids the toxicity inherent in thiol-containing compounds. It is capable of disrupting the botulinum neurotoxin B heavy-chain/light-chain complex that is held together by a single disulfide bond, and that is responsible for endocytosis, and ultimately the toxicity, of the toxin. Since disulfide-coupled subunits are characteristic of many toxins (e.g., ricin, snake venom, and all BoNT serotypes), it may be useful as a rescue prophylactic in cases of toxin administration.1

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