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Merck

PHR1050

Supelco

Benzoic acid

Pharmaceutical Secondary Standard; Certified Reference Material

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About This Item

Wzór liniowy:
C6H5COOH
Numer CAS:
Masa cząsteczkowa:
122.12
Beilstein:
636131
Numer WE:
Numer MDL:
Kod UNSPSC:
41116107
eCl@ss:
39023903
Identyfikator substancji w PubChem:
NACRES:
NA.24

klasa czystości

certified reference material
pharmaceutical secondary standard

Poziom jakości

agency

traceable to USP 1055002

gęstość pary

4.21 (vs air)

ciśnienie pary

10 mmHg ( 132 °C)

opis

API family: benfluorex

rodzina API

metronidazole, benfluorex, mefenamic acid

Certyfikat analizy

current certificate can be downloaded

temp. samozapłonu

1061 °F

metody

HPLC: suitable
gas chromatography (GC): suitable

tw

249 °C (lit.)

mp

121-125 °C (lit.)

Zastosowanie

cleaning products
cosmetics
food and beverages
personal care
pharmaceutical (small molecule)

format

neat

temp. przechowywania

2-30°C

ciąg SMILES

OC(=O)c1ccccc1

InChI

1S/C7H6O2/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H,8,9)

Klucz InChI

WPYMKLBDIGXBTP-UHFFFAOYSA-N

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Opis ogólny

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.

Zastosowanie

Benzoic acid may be used as a reference standard in determining the concentration of benzoic acid in food and milk samples using high performance liquid chromatography coupled with photodiode array detector (HPLC).

Komentarz do analizy

These secondary standards offer multi-traceability to the USP, EP (PhEur) and BP primary standards, where they are available.

Inne uwagi

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Przypis

To see an example of a Certificate of Analysis for this material enter LRAB8257 in the slot below. This is an example certificate only and may not be the lot that you receive.

Polecane produkty

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
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produkt powiązany

Numer produktu
Opis
Cennik

Piktogramy

Health hazardCorrosion

Hasło ostrzegawcze

Danger

Zwroty wskazujące rodzaj zagrożenia

Zwroty wskazujące środki ostrożności

Klasyfikacja zagrożeń

Eye Dam. 1 - Skin Irrit. 2 - STOT RE 1 Inhalation

Organy docelowe

Lungs

Kod klasy składowania

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Klasa zagrożenia wodnego (WGK)

WGK 1

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable


Choose from one of the most recent versions:

Certyfikaty analizy (CoA)

Lot/Batch Number

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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Klienci oglądali również te produkty

Determination of benzoic and sorbic acids in Brazilian food
Qi P, et al.
Food Control, 20, 414-418 (2009)
Determination of benzoic and sorbic acids in Brazilian food
Tfouni.V.A.S and Toledo F.C.M
Food Control, 13, 117-123 (2002)
S Nacht et al.
Journal of the American Academy of Dermatology, 4(1), 31-37 (1981-01-01)
The transepidermal penetration and metabolic disposition of 14C-benzoyl peroxide were assessed in vitro (excised human skin) and in vivo (rhesus monkey). In vitro, the benzoyl peroxide penetrated into the skin, through the stratum corneum or the follicular openings, or both
Ly Dieu Tran et al.
Journal of the American Chemical Society, 134(44), 18237-18240 (2012-10-30)
An auxiliary-assisted, copper catalyzed or promoted sulfenylation of benzoic acid derivative β-C-H bonds and benzylamine derivative γ-C-H bonds has been developed. The method employs disulfide reagents, copper(II) acetate, and DMSO solvent at 90-130 °C. Application of this methodology to the
Copper-mediated C-H/C-H biaryl coupling of benzoic acid derivatives and 1,3-azoles.
Mayuko Nishino et al.
Angewandte Chemie (International ed. in English), 52(16), 4457-4461 (2013-03-21)

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Ascentis® C18 column facilitates LC-UV/MS analysis of extractables from single-use systems, ensuring reliable identification and quantification.

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