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BHT

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    BHT
  • BHT
Cat No: 89910
Biochemicals - Ox Stress Reagents
Cayman

BHT is a synthetic antioxidant.{56221,56222} It scavenges peroxide, 2,2-diphenyl-1-picrylhydrazyl (DPPH; Item No. 14805), superoxide, and ABTS (Item No. 27317) radicals in cell-free assays, as well as inhibits lipid peroxidation of linoleic acid (Item...

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This product can only be bought through Cayman Chemical. Please contact us.

Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 2,6-di-tert-butyl-4-hydroxytoluene
Correlated keywords:
  • 2,6-di-tert-butyl-4-methylphenol butylhydroxytoluene ferroptosis 246 264 29 30 4 4K 501 DBPC KB MPJ OC T 501 T501 QT B-NOX BHT-P BAT Swanox CAO 1 3 Chemanox 11 Chinox Dalpac DBPC Deenax Dibunol Dibutyl paracresol Dibutylcresol Dibutylhydroxytoluene E 321 FG Grindox H-BHT Impruvol Ionol K-NOX-BHT Kerabit Lavinix Lowinox M 4801 Lubrizol 817 M 4801 Na-Lube AO 220 Naugard Nipanox NK Nocrac 200 2000 SP-N TBC Ralox NSC6347 P 21 parabar 441 permanax PN 01 popol selosol stavox sumilizer sustane swanox T 501 T501 T 502A T502A tenox tenamene 3 tonarol topanol C O O-FG OC OL ultranox 226 vanlube PCPCX vanox vianol vulkanox yoshinox
Product Overview:
BHT is a synthetic antioxidant.{56221,56222} It scavenges peroxide, 2,2-diphenyl-1-picrylhydrazyl (DPPH; Item No. 14805), superoxide, and ABTS (Item No. 27317) radicals in cell-free assays, as well as inhibits lipid peroxidation of linoleic acid (Item Nos. 90150
90150.1
21909) in vitro when used at a concentration of 45 µg/ml.{56221} BHT (0.025-3.2 mM) reduces freeze-thaw-induced malondialdehyde (MDA) production and increases sperm viability in boar spermatozoa preparations.{56222} Formulations containing BHT have been used as antioxidant cosmetic and food additives.
Size 500 mg
Shipping room temp.
CAS Number 128-37-0
Molecular Formula C15H24O
SMILES Cc1cc(c(O)c(c1)C(C)(C)C)C(C)(C)C
Molecular Weight 220,4
Formulation A crystalline solid
Purity ≥98%
Custom Code 2907.19
UNSPSC code 12352100

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Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

Accreditations
ISO/IEC 17025:2005
ISO Guide 34:2009

Cayman is a leader in the field of emerging drugs of abuse, providing high-purity Schedule I-V Controlled Substances to federally-licensed laboratories and qualified academic research institutions for forensic analyses. We are certified by ACLASS Accreditation Services with dual accreditation to ISO/IEC 17025:2005 and ISO Guide 34:2009.

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