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Merck
CN

8S61336

SS苯甲酸

2000 μg/mL in dichloromethane, analytical standard

别名:

苯甲酸 溶液

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关于此项目

经验公式（希尔记法）:
C7H6O2
化学文摘社编号:
65-85-0
分子量:
122.12
NACRES:
NA.24
UNSPSC Code:
41116107
EC Number:
200-838-9
MDL number:
MFCD00002398

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InChI key

WPYMKLBDIGXBTP-UHFFFAOYSA-N

InChI

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

grade

analytical standard

agency

EPA 8270

assay

99.90%

form

liquid

CofA

current certificate can be downloaded

packaging

ampule of 2.5 mL

concentration

2000 μg/mL in dichloromethane

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

cleaning products
cosmetics
food and beverages
personal care

format

single component solution

storage temp.

2-8°C

Other Notes

该产品即将下线。产品PHR1050-1G是其替代品。

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Warning

Hazard Classifications

Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Central nervous system

存储类别

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
LC25955V
LC23335V
LC11312
LC00786
LB75779

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  1. Which document(s) contains shelf-life or expiration date information for a given product?

    If available for a given product, the recommended re-test date or the expiration date can be found on the Certificate of Analysis.

  2. How do I get lot-specific information or a Certificate of Analysis?

    The lot specific COA document can be found by entering the lot number above under the "Documents" section.

  3. What does the "S" in Product No. 8S61336, Benzoic Acid, signify?

    The "S" signifies that 8S61336 is a Separate Source standard.  Separate Source standards are pairs of Supelco brand products having identical composition, in this case, 47508-U and 8S61336.  Each standard is prepared from independently sourced raw materials and are independently quality controlled.

  4. How is Product 8S61336, Benzoic Acid, Separate Source, packaged?

    The standard 8S61336 comes in a 5 mL amber ampule and contains slightly more than 2.5 mL.  This is to insure you that you can remove 2.5 mL from the container.

  5. How do I find price and availability?

    There are several ways to find pricing and availability for our products. Once you log onto our website, you will find the price and availability displayed on the product detail page. You can contact any of our Customer Sales and Service offices to receive a quote.  USA customers:  1-800-325-3010 or view local office numbers.

  6. What is the Department of Transportation shipping information for this product?

    Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product. 

  7. My question is not addressed here, how can I contact Technical Service for assistance?

    Ask a Scientist here.

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
Dajie Lin et al.
Biosensors & bioelectronics, 45, 195-200 (2013-03-19)
An amplification strategy for signal tracing was developed by introducing a host-guest binding reaction into the assembly process of gold nanorods (AuNRs) superstructure. The amplification pathway firstly used a thio-β-cyclodextrin (SH-β-CD) functionalized gold nanoparticles to label signal antibody, and then
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)
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
Deepankar Das et al.
Organic letters, 15(17), 4358-4361 (2013-08-21)
Redox-neutral formation of C-P bonds in the α-position of amines was achieved via a process that features a combination of an oxidative α-C-H bond functionalization and a reductive N-alkylation. Benzoic acid functions as an efficient catalyst in this three-component reaction
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