2,4-Difluoro-3-(methoxymethyl)benzoic+acid
Supplier:
AOB CHEM USA
Description:
1-(5-Bromo-2,3-difluoro-4-methylphenyl)ethanone ≥95%
Supplier:
AOB CHEM USA
Description:
2,3-Difluoro-4-(methylthio)benzaldehyde ≥95%
Catalog Number:
(89514-684)
Supplier:
Abgent
Description:
LEAF (Low Endotoxin, Azide-Free)
Supplier:
AOB CHEM USA
Description:
2-(2,6-Difluoro-4-isopropoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane ≥97%
Supplier:
AOB CHEM USA
Description:
Ethyl 2,3-difluoro-4-methoxybenzoate ≥97%
Supplier:
AMBEED, INC
Description:
2,3-Difluoro-4-iodoaniline 95%
Supplier:
TCI America
Description:
CAS Number: 2207-75-2
MDL Number: MFCD00010565 Molecular Formula: C4H3N3O4 Molecular Weight: 195.18 Purity/Analysis Method: >98.0% (HPLC,T) Form: Crystal Melting point (°C): 300
Supplier:
TCI America
Description:
Trans,Trans-4-(2,3-Difluoro-4-Methylphenyl)-4'-Ethylbicyclohexyl, Purity: >98.0%(GC), Cas no: 174350-08-4, Molecular formula : C21H30F2, Molecular weight : 320.47, Size: 5G
Supplier:
AMBEED, INC
Description:
1-Bromo-2,5-difluoro-4-(trifluoromethyl)benzene, Purity: 98%, CAS Number: 261945-75-9, Appearance: Colorless to Yellow Liquid, Storage: Sealed in dry, 2-8 deg C, Size: 250mg
Catalog Number:
(101833-582)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 032369-1G , MDL Number: MFCD11100522
Supplier:
AOB CHEM USA
Description:
Ethyl 2-(2-bromo-5,6-difluoro-3-methylphenyl)-2-oxoacetate ≥95%
Supplier:
Bachem Americas
Description:
Please see also α-MSH (corresponds to acetyl-ACTH (1-13) amide, H-1075), α-MSH (free acid) (acetyl-ACTH (1-13), H-1070), and (Des-acetyl)-α-MSH (H-4390). Wied: Pituitary Adrenal System Hormones and Behaviour. Symposium on Developments in Endocrinology (1976) / Anon.: ACTH and Related Peptides: Structure, Regulation, and Action. Ann. N.Y. Acad. Sci. 297, 1 (1977) / A.V.Schally: Aspects of Hypothalamic Regulation of the Pituitary Gland. Science 202, 18 (1978) / R.Schwyzer: Studies on Polypeptide Receptors. A Critical View on the Mechanism of ACTH Action. Bull. Schweiz. Acad. Med. Wiss. 34, 263 (1978).
Supplier:
MP Biomedicals
Description:
Storage: +4 °C
Pyruvic acid is an intermediate in sugar metabolism and in enzymatic carbohydrate degradation (alcoholic fermentation) where it is converted to acetaldehyde and CO2 by carboxylase. In muscle, pyruvic acid (derived from glycogen) is reduced to lactic acid during exertion, which is reoxidized and partially retransformed to glycogen during rest. It improves coliform recovery when present in culture medium. It is involved in a metabolic regulatory pathway activated by mitochondrial oxidants. Pyruvate is involved in respiratory regulation in plants by interacting with alternative oxidase at a conserved cysteine residue. It may help prevent hydrogen peroxide mediated cell death. Sodium pyruvate is utilized as a component in culture broth and media. Sodium pyruvate is used in Wallen fermentation medium to enhance the conversion of oleic acid to 10-ketostearic acid by Bacillus sphaericus. Sodium pyruvate has also been used to establish stably transfected human B cell lines. Sodium Pyruvate has shown antioxidant properties and protective effects against oxygen radicals. Pyruvate is produced as part of glycolysis and is an intermediate in many metabolic pathways. It can be converted into acetyl CoA and enter the TCA Cycle.
Supplier:
AOB CHEM USA
Description:
Ethyl 2-(2,6-difluoro-3-(methylthio)phenyl)-2-oxoacetate ≥95%
Catalog Number:
(76076-006)
Supplier:
Prosci
Description:
For WB starting dilution is: 1:1000 For IHC-P starting dilution is: 1:50~100
Supplier:
AOB CHEM USA
Description:
2,2-Difluoro-1-(2-methyl-3-(trifluoromethyl)phenyl)ethanone ≥95%
Inquire for Price
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
![]()
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
![]()
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at 1-800-932-5000.
|
|||||||||