Succinic acid BioXtra, ≥99.0%

Properties

Related Categories	Building Blocks, C1 to C5, Carbonyl Compounds, Carboxylic Acids, Chemical Synthesis, Organic Building Blocks More...
product line	BioXtra
assay	≥99.0%
impurities	≤0.0005% Phosphorus (P)
	≤0.01% Insoluble matter
ign. residue	≤0.02%
bp	235 °C(lit.)
mp	184-186 °C(lit.)
solubility	H₂O: soluble0.5 M, clear, colorless
anion traces	chloride (Cl^-): ≤0.001%
	sulfate (SO₄^2-): ≤0.003%
cation traces	Al: ≤0.0005%
	Ca: ≤0.001%
	Cu: ≤0.0005%
	Fe: ≤0.0005%
	K: ≤0.005%
	Mg: ≤0.0005%
	NH₄⁺: ≤0.05%
	Na: ≤0.005%
	Pb: ≤0.001%
	Zn: ≤0.0005%

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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)

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Certificate of Analysis

Certificate of Origin

Pressure-Temperature Nomograph

S3674 - Product Information Sheet (48 KB)

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

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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)

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

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

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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)

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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)

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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)

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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)

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

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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

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Succinic acid

BioXtra, ≥99.0%

Properties

Price and Availability

Related Papers

Documents

Safety Information

Papers

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