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2,6-Di-tert-butyl-4-methylphenol - Ultra pure,>99.5%(GC), high purity , CAS No.128-37-0

  • Ultra pure
  • ≥99.5%(GC)
Item Number
D104366
Grouped product items
SKUSizeAvailabilityPrice Qty
D104366-500g
500g
In stock
$58.90

Basic Description

Synonyms2,6-Di-tert-butyl-4-methylphenol|128-37-0|Butylhydroxytoluene|2,6-Di-tert-butyl-p-cresol|2,6-Di-t-butyl-4-methylphenol|Ionol|DBPC|Stavox|BHT|Impruvol|Ionol CP|Dalpac|Deenax|Dibunol|Ionole|Kerabit|Topanol|Vianol|Antioxidant KB|Antioxidant 4K|Sumilizer BHT|
Specifications & PurityUltra pure, ≥99.5%(GC)
Biochemical and Physiological Mechanisms二丁基羟基甲苯 (BHT) 是一种酚类抗氧化剂。它可以抑制脂类过氧化。它会导致小鼠肺部损伤以及促进肿瘤生长,这可能是由于 BHT 的代谢产物造成,即 6-叔丁基-2-[2′-(2′-羟基甲基)-丙基]-4-甲基苯酚。还报道了 BHT 的代谢产物会引起培养细胞中的 DNA 链断裂以及核小体间 DNA 断裂(细胞凋亡的典型特征)。向大鼠进行单次 BHT 腹腔注射(60mg/kg 体重)会引起肝、肾、心脏、脾、大脑和肺部的核 DNA 甲基转移酶活动的显著提高。用 BHT 孵育肺泡巨噬细胞可以显著降低 TNF-α
Storage TempProtected from light,Argon charged
Shipped InNormal
GradeUltra pure
Product Description

An antioxidant shown to be chemopreventive against a variety of carcinogens.

Associated Targets

CYP1A2 Tchem Cytochrome P450 1A2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP2D6 Tclin Cytochrome P450 2D6 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP2C19 Tchem Cytochrome P450 2C19 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP3A4 Tclin Cytochrome P450 3A4 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

POLB Tchem DNA polymerase beta 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP2C9 Tchem Cytochrome P450 2C9 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GMNN Tbio Geminin 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PTH1R Tclin Parathyroid hormone/parathyroid hormone-related peptide receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

VDR Tclin Vitamin D3 receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HDAC6 Tclin Histone deacetylase 6 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TXNRD1 Tclin Thioredoxin reductase 1, cytoplasmic 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SMN1 Tchem Survival motor neuron protein 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

RXRA Tclin Retinoic acid receptor RXR-alpha 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

UGT1A9 Tbio UDP-glucuronosyltransferase 1-9 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PLK1 Tchem Serine/threonine-protein kinase PLK1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NR1H4 Tclin Bile acid receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA1 Tclin Carbonic anhydrase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA2 Tclin Carbonic anhydrase 2 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CAPN1 Tchem Calpain-1 catalytic subunit 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ALDH1A1 Tchem Retinal dehydrogenase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

UGT1A6 Tbio UDP-glucuronosyltransferase 1-6 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KCNH2 Tclin Potassium voltage-gated channel subfamily H member 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PPARA Tclin Peroxisome proliferator-activated receptor alpha 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NFE2L2 Tchem Nuclear factor erythroid 2-related factor 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CXCL8 Tchem Interleukin-8 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NOS1 Tchem Nitric oxide synthase, brain 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NFKB1 Tclin Nuclear factor NF-kappa-B p105 subunit 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NOS3 Tchem Nitric oxide synthase, endothelial 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 2,6-ditert-butyl-4-methylphenol
INCHI InChI=1S/C15H24O/c1-10-8-11(14(2,3)4)13(16)12(9-10)15(5,6)7/h8-9,16H,1-7H3
InChi Key NLZUEZXRPGMBCV-UHFFFAOYSA-N
Canonical SMILES CC1=CC(=C(C(=C1)C(C)(C)C)O)C(C)(C)C
Isomeric SMILES CC1=CC(=C(C(=C1)C(C)(C)C)O)C(C)(C)C
RTECS GO7875000
PubChem CID 31404
Molecular Weight 220.35
Beilstein 6(3)2073
Reaxy-Rn 1911640

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

11 results found

Lot NumberCertificate TypeDateItem
I2403305Certificate of AnalysisAug 27, 2024 D104366
I2403311Certificate of AnalysisAug 27, 2024 D104366
G2205459Certificate of AnalysisApr 03, 2024 D104366
B2429221Certificate of AnalysisFeb 18, 2024 D104366
B2429224Certificate of AnalysisFeb 18, 2024 D104366
A2425011Certificate of AnalysisJan 30, 2024 D104366
J2320216Certificate of AnalysisOct 11, 2023 D104366
G2205108Certificate of AnalysisJun 08, 2022 D104366
C2208179Certificate of AnalysisFeb 18, 2022 D104366
C2208183Certificate of AnalysisFeb 18, 2022 D104366
G2115173Certificate of AnalysisJun 29, 2021 D104366

more

Chemical and Physical Properties

SolubilitySoluble in ethanol (100 mg/ml), chloroform, DMSO (≥30 mg/ml), and DMF (≥ 30 mg/ml). Insoluble in water(0.6 mg/ml),toluene, isopropanol, methyl ethyl ketone, acetone, benzene, petroleum ether and ethanol.
SensitivityLight sensitive;Air sensitive
Refractive Index1.4859
Flash Point(°F)260°F
Flash Point(°C)(open)127℃
Boil Point(°C)265°C
Melt Point(°C)70°C

Safety and Hazards(GHS)

Pictogram(s) GHS09
Signal Warning
Hazard Statements

H400:Very toxic to aquatic life

H410:Very toxic to aquatic life with long lasting effects

Precautionary Statements

P273:Avoid release to the environment.

P501:Dispose of contents/container to ...

P391:Collect spillage.

RTECS GO7875000
Reaxy-Rn 1911640
Class 9
Merck Index 1548

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