Succinic acid, ACS reagent, ≥99.0% | HOOCCH2CH2COOH

Properties

Related Categories	ACS Grade, Building Blocks, C1 to C5, Carbonyl Compounds, Carboxylic Acids, Chemical Synthesis, Essential Chemicals, Inorganic Salts, Solutions and Reagents, Organic Building Blocks, Research Essentials More...
grade	ACS reagent
assay	≥99.0%
impurities	≤0.001% N compounds
	≤0.01% insolubles
ign. residue	≤0.02%
bp	235 °C(lit.)
mp	184-186 °C(lit.)
anion traces	chloride (Cl^-): ≤0.001%
	phosphate (PO₄^3-): ≤0.001%
	sulfate (SO₄^2-): ≤0.003%
cation traces	Fe: ≤5 ppm
	heavy metals (as Pb): ≤5 ppm

Show More (13)

Description

Packaging

1 kg in poly bottle

500 g in poly bottle

Price and Availability

Related Papers

Hexylitaconic acid: a new inhibitor of p53-HDM2 interaction isolated from a marine-derived fungus, Arthrinium sp. Sachiko Tsukamoto et al Bioorg. Med. Chem. Lett. 16, 69-71, (2006)

Documents

Certificate of Analysis

Certificate of Origin

398039 Product Infromation Sheet (26 KB )

Pressure-Temperature Nomograph

Safety Information

Symbol	GHS05, GHS07
Signal word	Danger
Hazard statements	H315-H318-H335
Precautionary statements	P261-P280-P305 + P351 + P338
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes (Europe)	Xi
Risk Statements (Europe)	37/38-41
Safety Statements (Europe)	26-36/37/39
WGK Germany	1
RTECS	WM4900000

Technical information & documentation associated with this product is available in the Safety & Documentation tab.

Papers

Set your institution to view full text papers.

Hexylitaconic acid: a new inhibitor of p53-HDM2 interaction isolated from a marine-derived fungus, Arthrinium sp. Sachiko Tsukamoto et al Bioorg. Med. Chem. Lett. 16, 69-71, (2006)

Loading...

Coupling substrate and ion binding to extracellular gate of a sodium-dependent aspartate transporter. Olga Boudker et al Nature 445, 387-93, (2007)

Loading...

Inhibitor scaffolds for 2-oxoglutarate-dependent histone lysine demethylases. Nathan R Rose et al J. Med. Chem. 51, 7053-6, (2008)

Loading...

Development of a phospholipidosis database and predictive quantitative structure-activity relationship (QSAR) models. Naomi L Kruhlak et al Toxicol. Mech. Methods 18, 217-27, (2008)

Loading...

Application of a proteolysis/mass spectrometry method for investigating the effects of inhibitors on hydroxylase structure. Christopher J Stubbs et al J. Med. Chem. 52, 2799-805, (2009)

Loading...

Molecular modifications on carboxylic acid derivatives as potent histone deacetylase inhibitors: Activity and docking studies. Gamze Bora-Tatar et al Bioorg. Med. Chem. 17, 5219-28, (2009)

Loading...

Effects of structural analogues of the substrate and allosteric regulator of the human mitochondrial NAD(P)+-dependent malic enzyme. Kuo-Liang Su et al Bioorg. Med. Chem. 17, 5414-9, (2009)

Loading...

Using NMR solvent water relaxation to investigate metalloenzyme-ligand binding interactions. Ivanhoe K H Leung et al J. Med. Chem. 53, 867-75, (2010)

Loading...

Merck 14,8869

Beil. 2,IV,1908

Aldrich MSDS 1, 1624:B / Arctander, 2867 / Corp MSDS 1 (2), 3188:C / FT-IR 1 (1), 492:A / FT-IR 2 (1), 769:D / FT-NMR 1 (1), 766:B / IR-Spectra (2), 260:H / IR-Spectra (3), 289:E / NMR-Reference 2 (1), 428:C / RegBook 1 (1), 541:J / RegBook 67 (1), 541:J / Sax 6, 2476 / Sigma FT-IR 1 (2), 892:D / Structure Index 1, 76:B:7

EMAIL THIS PAGE TO A FRIEND

Succinic acid

ACS reagent, ≥99.0%

Properties

Description

Packaging

Price and Availability

Related Papers

Documents

Safety Information

Papers

Technical Service:

Bulk Ordering & Pricing: