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Merck

1083008

USP

2-tert-Butyl-4-hydroxyanisole

United States Pharmacopeia (USP) Reference Standard

Synonim(y):

2-BHA, 3-(1,1-Dimethylethyl)-4-methoxyphenol, 3-tert-Butyl-4-methoxyphenol

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Wybierz wielkość

200 MG

2290,00 zł

2290,00 zł


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Informacje o tej pozycji

Wzór empiryczny (zapis Hilla):
C11H16O2
Numer CAS:
Masa cząsteczkowa:
180.24
MDL number:
UNSPSC Code:
41116107
NACRES:
NA.24

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SMILES string

O(C)c1c(cc(cc1)O)C(C)(C)C

InChI

1S/C11H16O2/c1-11(2,3)9-7-8(12)5-6-10(9)13-4/h5-7,12H,1-4H3

InChI key

IMOYOUMVYICGCA-UHFFFAOYSA-N

grade

pharmaceutical primary standard

API family

butylhydroxyanisole

manufacturer/tradename

USP

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

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Ta pozycja
PHR2336PHR130620021
grade

pharmaceutical primary standard

grade

certified reference material, pharmaceutical secondary standard

grade

certified reference material, pharmaceutical secondary standard

grade

-

manufacturer/tradename

USP

manufacturer/tradename

-

manufacturer/tradename

-

manufacturer/tradename

-

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical small molecule

application(s)

pharmaceutical (small molecule)

application(s)

-

format

neat

format

-

format

neat

format

-

API family

butylhydroxyanisole

API family

butylhydroxyanisole

API family

bha

API family

-

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-30°C

storage temp.

-

General description

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

Application

2-tert-Butyl-4-hydroxyanisole USP reference standard, intended for use in specified quality tests and assays as specified in the USP compendia.

Analysis Note

These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.  ​

Other Notes

Sales restrictions may apply.
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comparable product

Numer produktu
Opis
Cennik

related product

pictograms

Environment

hcodes

Hazard Classifications

Aquatic Chronic 2

Klasa składowania

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable


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Certyfikaty analizy (CoA)

Lot/Batch Number

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Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

P A Schilderman et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 29(2), 79-85 (1991-02-01)
To determine the effects of dietary ethanol or fibre on 2(3)-tert-butyl-4-hydroxyanisole (BHA)-induced alterations in cell kinetics in gastro-intestinal tract tissues, groups of six male Wistar rats were fed diets containing 0% (control) or 1.5% BHA for 2 wk. One group
H Nishiya et al.
Pharmacology, 39(4), 213-223 (1989-01-01)
Binding of cefpiramide (CPM) and other beta-lactam antimicrobial agents to 2(3)-tert-butyl-4-hydroxyanisole (BHA)-induced liver glutathione (GSH) S-transferases (EC 2.5.1.18) from CD-1 mice was studied. A marked induction of hepatic GSH S-transferase from mice fed BHA was observed. Gel chromatography of liver
Laura Romero et al.
Molecular pharmacology, 70(1), 277-286 (2006-04-13)
The regulation of human GSTA1 by chemical inducers of rodent glutathione S-transferases (GSTs) and the regulatory role of hepatic nuclear factor (HNF) 1 was investigated in Caco-2 cells. Treatment of preconfluent and confluent cells with 12-O-tetra-decanoyl phorbol-13-acetate (TPA), 3-methylcholanthrene (3-MC)
J M Menter et al.
Melanoma research, 3(6), 443-449 (1993-12-01)
Certain mono- and dihydroxybenzene derivatives are selectively cytotoxic for melanocytes in vivo, and can cause depigmentation of skin and hair. We produced selective melanocytotoxicity/hair depigmentation in C57Bl mice by injection of 0.032-1.0% p-t-butylcatechol (tBC) or p-hydroxyanisole (MMEH) in physiological saline.
H S Mahal et al.
Free radical biology & medicine, 26(5-6), 557-565 (1999-04-28)
Various one-electron oxidants such as OH*, tert-BuO*, CCl3OO*, Br2*- and N3*, generated pulse radiolytically in aqueous solutions at pH 7, were scavenged by melatonin to form two main absorption bands with lambda(max) = 335 nm and 500 nm. The assignment

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