Quality Management Dossier; Operational Excellence Dossier; SDS; CoA; Certificates ; Material Qualification Dossier; Synonyms: Butanedioic acid Molar Mass: 118.09 g/mol Chemical Formula: HOOCCH₂CH₂COOH EC Number: 203-740-4 Hill Formula: C₄H₆O₄ CAS #: 110-15-6 … Help. Insoluble Solubility in chloroform: Soluble Related compounds Related Monomers. esters are used as flavouring base materials, plasticizers, solvent carriers and Help. Acid(Butanedioic Acid), 185 2. IDENTIFICATION, GENERAL c acid cycle. esters are used as in a variety of direct and indirect applications. Moderately toxic and an irritant. REQUIREMENTS Assay: 99.0% HOOCCH2CH2COOH Melting point: 185C-191C . (-)-4'-desmethyl-epipodophyllotoxin biosynthesis, 2-oxoglutarate + L-arginine + oxygen -> succinate + CO2 + guanidinium + (S)-1-pyrroline-5-carboxylate + H2O + H+, 3 2-oxoglutarate + L-arginine + 3 oxygen + 3 H+ -> 2 ethene + 7 CO2 + succinate + guanidinium + (S)-1-pyrroline-5-carboxylate + 3 H2O, a (2R,3S,4S)-leucoanthocyanidin + 2-oxoglutarate + oxygen + H+ -> an anthocyanidin with a 3-hydroxy group + succinate + CO2 + 2 H2O, aerobic respiration III (alternative oxidase pathway), anthocyanin biosynthesis (delphinidin 3-O-glucoside), anthocyanin biosynthesis (pelargonidin 3-O-glucoside), fumarate[in] + a menaquinol[membrane] -> succinate[in] + a menaquinone[membrane], fumarate[in] + a rhodoquinol[membrane] -> succinate[in] + a rhodoquinone[membrane], fumarate[in] + an electron-transfer quinol[membrane] -> succinate[in] + an electron-transfer quinone[membrane], gibberellin biosynthesis I (non C-3, non C-13 hydroxylation), gibberellin biosynthesis II (early C-3 hydroxylation), gibberellin biosynthesis III (early C-13 hydroxylation), gibberellin inactivation I (2beta-hydroxylation), homocysteine and cysteine interconversion, hydroxylated mugineic acid phytosiderophore biosynthesis, leucopelargonidin and leucocyanidin biosynthesis, pentalenolactone D + 2 2-oxoglutarate + 2 oxygen -> pentalenolactone F + 2 succinate + 2 CO2 + H2O, polymethylated quercetin glucoside biosynthesis I - quercetin series (Chrysosplenium), polymethylated quercetin glucoside biosynthesis II - quercetagetin series (Chrysosplenium), proanthocyanidins biosynthesis from flavanols, succinate[in] + a ubiquinone[membrane] -> fumarate[in] + an ubiquinol[membrane], succinate[in] + an electron-transfer quinone[membrane] -> fumarate[in] + an electron-transfer quinol[membrane], succinate[mitochondrial lumen] + a ubiquinone[mitochondrial lumen] -> fumarate[mitochondrial lumen] + an ubiquinol[mitochondrial lumen], superpathway of glyoxylate cycle and fatty acid degradation, superpathway of hyoscyamine and scopolamine biosynthesis, superpathway of scopolin and esculin biosynthesis, (-)-yatein + 2-oxoglutarate + oxygen -> (-)-deoxypodophyllotoxin + succinate + CO2 + H2O, (+)-dihydrokaempferol + 2-oxoglutarate + oxygen -> kaempferol + succinate + CO2 + H2O + H+, (+)-dihydromyricetin + 2-oxoglutarate + oxygen -> myricetin + succinate + CO2 + H2O, (+)-taxifolin + 2-oxoglutarate + oxygen -> quercetin + succinate + CO2 + H2O, (2R,3S,4S)-leucodelphinidin + 2-oxoglutarate + oxygen -> delphinidin + CO2 + succinate + H+ + 2 H2O, (2R,3S,4S)-leucopelargonidin + 2-oxoglutarate + oxygen -> (4S)-2,3-dehydroleucopelargonidin + succinate + CO2 + H2O + 2 H+, (2S)-dihydrotricetin + 2-oxoglutarate + oxygen -> (+)-dihydromyricetin + succinate + CO2, (2S)-eriodictyol + 2-oxoglutarate + oxygen -> (+)-taxifolin + CO2 + succinate, (2S)-eriodictyol + 2-oxoglutarate + oxygen -> (+)-taxifolin + succinate + CO2, (2S)-eriodictyol + 2-oxoglutarate + oxygen -> luteolin + succinate + CO2 + H2O, (2S)-naringenin + 2-oxoglutarate + oxygen -> (+)-dihydrokaempferol + succinate + CO2, (2S)-naringenin + 2-oxoglutarate + oxygen -> apigenin + succinate + CO2 + H2O + H+, (2S)-naringenin + 2-oxoglutarate + oxygen -> CO2 + succinate + (+)-dihydrokaempferol, (2S)-pinocembrin + 2-oxoglutarate + oxygen -> (+)-pinobanksin + CO2 + succinate, (2S)-pinocembrin + 2-oxoglutarate + oxygen -> (+)-pinobanksin + succinate + CO2, (2S)-pinocembrin + 2-oxoglutarate + oxygen -> chrysin + succinate + CO2 + H2O, (6S)-hydroxyhyoscyamine + 2-oxoglutarate + oxygen -> scopolamine + succinate + CO2 + H+ + H2O, (S)-atropinium + 2-oxoglutarate + oxygen -> (6S)-hydroxyhyoscyamine + succinate + CO2, (S)-dihydroorotate + fumarate -> orotate + succinate, 2'-deoxymugineate + 2-oxoglutarate + oxygen -> 3-epihydroxy-2'-deoxymugineate + succinate + CO2 + H+, 2'-deoxymugineate + 2-oxoglutarate + oxygen -> mugineate + succinate + CO2 + H+, 2-oxoglutarate + (S)-atropinium + oxygen -> CO2 + succinate + (6S)-hydroxyhyoscyamine, 2-oxoglutarate + 3,7,4'-trimethylquercetin + 3,7,4'-trimethylquercetin + 2-oxoglutarate + oxygen + oxygen -> CO2 + succinate + 3,7,4'-trimethylquercetagetin + succinate + CO2, 2-oxoglutarate + 3,7-dimethylquercetin + 3,7-dimethylquercetin + 2-oxoglutarate + oxygen + oxygen -> CO2 + succinate + 3,7-dimethylquercetagetin + 3,7-dimethylquercetagetin + succinate + CO2, 2-oxoglutarate + 8-hydroxy-salvigenin + 2-oxoglutarate + oxygen + oxygen -> CO2 + succinate + formaldehyde + pilosin + formaldehyde + succinate + CO2, 2-oxoglutarate + apiforol + 2-oxoglutarate + oxygen + oxygen -> CO2 + succinate + apigeninidin + succinate + CO2 + 2 H2O + 2 H2O, 2-oxoglutarate + desacetoxyvindoline + oxygen -> CO2 + succinate + 17-O-deacetylvindoline, 2-oxoglutarate + gardenin B + 2-oxoglutarate + oxygen + oxygen -> CO2 + succinate + formaldehyde + nevadensin + formaldehyde + succinate + CO2, 2-oxoglutarate + luteoforol + 2-oxoglutarate + H+ + oxygen + oxygen + H+ -> CO2 + succinate + luteolinidin + succinate + CO2 + 2 H2O + 2 H2O, 3,7,4'-trimethylquercetin + 2-oxoglutarate + oxygen -> 3,7,4'-trimethylquercetagetin + succinate + CO2, 4-coumaroyl-CoA + 2-oxoglutarate + oxygen -> 2,4-dihydroxycinnamoyl-CoA + succinate + CO2, a (2R,3S,4S)-leucoanthocyanidin + 2-oxoglutarate + oxygen -> a (4S)- 2,3-dehydroflavan-3,4-diol + succinate + CO2 + H2O, apiforol + 2-oxoglutarate + oxygen -> apigeninidin + succinate + CO2 + 2 H2O, codeine + 2-oxoglutarate + oxygen -> morphine + formaldehyde + succinate + CO2, desacetoxyvindoline + 2-oxoglutarate + oxygen -> 17-O-deacetylvindoline + succinate + CO2, desacetoxyvindorosine + 2-oxoglutarate + oxygen -> deacetylvindorosine + succinate + CO2, DIBOA-beta-D-glucoside + 2-oxoglutarate + oxygen -> TRIBOA-beta-D-glucoside + succinate + CO2, D-threo-isocitrate -> glyoxylate + succinate, ferulate + 2-oxoglutarate + oxygen -> (E)-6'-hydroxyferulate + succinate + CO2, feruloyl-CoA + 2-oxoglutarate + oxygen -> 6'-hydroxyferuloyl-CoA + succinate + CO2, fumarate[in] + 2 H+[in] + 2 e-[membrane] -> succinate[in], gamma-butyrobetaine + 2-oxoglutarate + oxygen -> L-carnitine + succinate + CO2, gibberellin A1 + 2-oxoglutarate + oxygen -> gibberellin A8 + succinate + CO2, gibberellin A12 + 2-oxoglutarate + oxygen -> gibberellin A110 + succinate + CO2, gibberellin A12 + 2-oxoglutarate + oxygen -> gibberellin A14 + succinate + CO2, gibberellin A12 + 2-oxoglutarate + oxygen -> gibberellin A15 (open lactone form) + CO2 + succinate, gibberellin A12 + 2-oxoglutarate + oxygen -> gibberellin A15 (open lactone form) + succinate + CO2, gibberellin A12 + 2-oxoglutarate + oxygen -> gibberellin A53 + succinate + CO2, gibberellin A14 + 2-oxoglutarate + oxygen -> gibberellin A37 + CO2 + succinate, gibberellin A15 (open lactone form) + 2-oxoglutarate + oxygen -> gibberellin A24 + CO2 + succinate + H2O, gibberellin A15 (open lactone form) + 2-oxoglutarate + oxygen -> gibberellin A24 + succinate + CO2 + H2O, gibberellin A15 (open lactone form) + 2-oxoglutarate + oxygen -> gibberellin A37 + succinate + CO2, gibberellin A19 + 2-oxoglutarate + oxygen -> gibberellin A17 + succinate + CO2 + H+, gibberellin A19 + 2-oxoglutarate + oxygen -> gibberellin A20 + 2 CO2 + succinate + H+, gibberellin A20 + 2-oxoglutarate + oxygen -> gibberellin A1 + succinate + CO2, gibberellin A20 + 2-oxoglutarate + oxygen -> gibberellin A29 + succinate + CO2, gibberellin A24 + 2-oxoglutarate + oxygen -> gibberellin A25 + CO2 + succinate + H+, gibberellin A24 + 2-oxoglutarate + oxygen -> gibberellin A36 + succinate + CO2, gibberellin A24 + 2-oxoglutarate + oxygen -> gibberellin A9 + 2 CO2 + succinate + H+, gibberellin A25 + 2-oxoglutarate + oxygen -> gibberellin A13 + succinate + CO2, gibberellin A29 + 2-oxoglutarate + oxygen -> gibberellin A29-catabolite + succinate + CO2 + H+ + H2O, gibberellin A34 + 2-oxoglutarate + oxygen -> gibberellin A34-catabolite + succinate + CO2 + H+ + H2O, gibberellin A36 + 2-oxoglutarate + NADP+ + oxygen -> gibberellin A4 + succinate + 2 CO2 + NADPH, gibberellin A37 + 2-oxoglutarate + oxygen -> gibberellin A36 + succinate + CO2 + H2O, gibberellin A4 + 2-oxoglutarate + oxygen -> gibberellin A34 + succinate + CO2, gibberellin A44 (closed lactone form) + 2-oxoglutarate + 2 H+ + oxygen -> gibberellin A98 + succinate + CO2, gibberellin A5 + 2-oxoglutarate + oxygen -> gibberellin A3 + succinate + CO2, gibberellin A5 + 2-oxoglutarate + oxygen -> gibberellin A6 + succinate + CO2, gibberellin A51 + 2-oxoglutarate + oxygen -> gibberellin A51-catabolite + succinate + CO2 + H+ + H2O, gibberellin A53 + 2-oxoglutarate + oxygen -> gibberellin A97 + succinate + CO2, gibberellin A53 + 2-oxoglutarate + oxygen -> gibberellin44 (open lactone form) + CO2 + succinate, gibberellin A8 + 2-oxoglutarate + oxygen -> gibberellin A8-catabolite + succinate + CO2 + H+ + H2O, gibberellin A9 + 2-oxoglutarate + oxygen -> gibberellin A4 + succinate + CO2, gibberellin A9 + 2-oxoglutarate + oxygen -> gibberellin A51 + succinate + CO2, gibberellin44 (open lactone form) + 2-oxoglutarate + H+ + oxygen -> gibberellin A38 + succinate + CO2 + H2O, gibberellin44 (open lactone form) + 2-oxoglutarate + oxygen -> gibberellin A19 + succinate + CO2 + H2O, L-arginine + 2-oxoglutarate + oxygen -> (3S)-3-hydroxy-L-arginine + succinate + CO2, L-cysteine + O-succinyl-L-homoserine <--> succinate + L-cystathionine + H+, luteoforol + 2-oxoglutarate + oxygen + H+ -> luteolinidin + succinate + CO2 + 2 H2O, mugineate + 2-oxoglutarate + oxygen -> 3-epihydroxymugineate + succinate + CO2, N6,N6,N6-trimethyl-L-lysine + 2-oxoglutarate + oxygen -> 3-hydroxy-N6,N6,N6-trimethyl-L-lysine + succinate + CO2, N-succinyl-L,L-2,6-diaminopimelate + H2O -> L,L-diaminopimelate + succinate, oripavine + 2-oxoglutarate + oxygen -> morphinone + formaldehyde + succinate + CO2, O-succinyl-L-homoserine + L-cysteine <--> L-cystathionine + succinate + H+, pentalenolactone D + 2-oxoglutarate + oxygen -> pentalenolactone E + succinate + CO2 + H2O, pentalenolactone E + 2-oxoglutarate + oxygen -> pentalenolactone F + succinate + CO2, succinate + ATP + coenzyme A <--> succinyl-CoA + ADP + phosphate, succinate + GTP + coenzyme A <--> succinyl-CoA + GDP + phosphate, succinate semialdehyde + NAD+ + H2O -> succinate + NADH + 2 H+, thebaine + 2-oxoglutarate + oxygen -> neopinone + formaldehyde + succinate + CO2, thebaine + 2-oxoglutarate + oxygen -> oripavine + formaldehyde + succinate + CO2, trans-caffeoyl-CoA + 2-oxoglutarate + oxygen -> 2,4,6-trihydroxycinnamoyl-CoA + succinate + CO2. Succinic acid is a dicarboxylic acid with the chemical formula (CH2)2(CO2H)2. Melting Point >186ºC (dec.) Molecular Weight: 122.06: Storage: Refrigerator: Solubility: Methanol (Slightly), Water (Slightly) Category: Building Blocks; Isotopic Labeled Analogues; Applications: Succinic Acid-13C4 is a compound useful in organic synthesis. Human Metabolome Database (HMDB)-21 °C. Succinic acid. 11, 109 Succinic acid, also called Butanedioic Acid, a dicarboxylic acid of molecular formula C 4 H 6 O 4 that is widely distributed in almost all plant and animal tissues and that plays a significant role in intermediary metabolism. C, 302 C, 265 - 110 C, C It has been replaced with USP Succinic Acid Melting Point Standard (Approximately 186 degrees) RS Catalog # 1623422. 99.0 % Melting point: 185.0 to 189.0 °C: Solubility in hot Water The name derives from Latin succinum, meaning amber. Higher chain compounds are used as components in metalworking at 100 mmHg, C It is marketed as food additive E363. SpectraBase Compound ID: l9lM5r2ysb: Mol Weight: 0.0 g/mol: Molecular Formula: C4H6O4: Exact Mass: 0.0 g/mol: Transmission Infrared (IR) Spectrum. Characteristics of "Succinic Acid" "Succinic Acid" is distributed widely through the natural world, where it is contained in bivalves, fossils, seaweed, lichen, bacteria and so on. - 129 C, 245 Environmental: Succinic acid is not expected to volatilize from water surfaces. Product Name & Other Names: Succinic Acid or Butanedioic acid. 1.3 Details of the supplier of the safety data sheet Company : Central Drug House (P) Ltd 7/28 Vardaan House New Delhi-10002 INDIA Telephone : +91 11 49404040 Email : care@cdhfinechemical.com 1.4 … CopyCopied, Validated by Experts, Validated by Users, Non-Validated, Removed by Users, Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module, Predicted data is generated using the US Environmental Protection Agency’s EPISuite™, Click to predict properties on the Chemicalize site, For medical information relating to Covid-19, please consult the, https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:15741, ACD/Labs Percepta Platform - PhysChem Module, US Environmental Protection Agency’s EPISuite™, Compounds with the same molecular formula, Search Google for structures with same skeleton, Soluble in water (increasing with temperature). Succinic Acid or Butanedioic Acid SDS, Safety Data Sheet MSDS, Material Safety Data Sheet 20-Nov-20. fluids, surfactants, lubricants, detergents, oiling agents, emulsifiers, wetting acid, arboxylic acid can An alpha,omega-dicarboxylic acid resulting from the formal oxidation of each of the terminal methyl groups of butane to the corresponding carboxy group. Substances to be avoided include strong bases,strong oxidizing agents. Krebs cycle (also called citric acid cycle; tricarboxylic acid cycle) is a Sign In. Succinic Acid is widely used in industry Like Food Inductry, Pharmaceutical Industry, Adhesive 19.1 mg/mL at 25 °C. EPA DSSTox. The full spectrum can only be viewed using a FREE account. 16, 124 treatment chemical, vehicle water cooling systems and Succinate is a component of the citric acid cycle and is capable of donating electrons to the electron … PRODUCT IDENTIFICATION. Download MSDS File. Phenylsuccinate. 1 Structures Expand this section. Stable. catalytic hydrogenation of maleic acid or its anhydride. Chemsrc provides Succinic acid(CAS#:110-15-6) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. # DEREK, a knowledge-based systemr epeatedly cited in the Guidance on information requirements and chemical safety assessment, Chapter R.6 "QSARs and grouping of chemicals" was applied to succinic acid and also to the chemically analogous substances fumaric acid and maleic acid. The melting temperature of succinic acid is 185 - 187 °C. It is a diprotic acid. - 134 Appearance: White powder to crystal: Purity(GC) min. Succinic acid is a colourless crystalline solid with a melting point of 185 -187 C soluble in water slightly dissolved in ethanol, ether, acetone and glycerine not dissolved in benzene, carbon sulfide, carbon tetrachloride and oil ether. vitamins) and agrochemicals … AND CHEMICAL PROPERTIES, moderately CopyCopied, KDYFGRWQOYBRFD-UHFFFAOYSA-N acid of four carbon atoms. carbon sulfide, carbon tetrachloride and oil ether. & MALEIC ACID, GENERAL Does anyone know? 18, Octadecanedioic infinite esters obtained from carboxylic Combustible. Get info of suppliers, manufacturers, exporters, traders of Succinic Acid for buying in India. Tetrahydrofuran (THF) was used as an eluent at a flow rate of 1.0 mL/min at 40 °C. Other names. ILO International Chemical Safety Cards (ICSC) 3.2.5 Solubility. It occurs naturally in plant Sulfapyridine Melting Point Standard (1 g) (Approximately 191 degrees) DISCONTINUED: This item has been discontinued and is no longer available for purchase. Often you don’t even need to prepare a fresh sample, because after cooling the melted sample ... Succinic acid 184-185 Learning goals: • Learn how to run a melting point device and measure melting range EPA DSSTox-21°C. Acid(Heptanedioic Acid), 105 length (Straight), CAS It is soluble in water and slightly soluble in ethanol for the preparation of pentaheterocyclic compounds.Specification:Test ItemsSp Acid). C at 15 mmHg, C Acid), C CopyCopied, InChI=1S/C4H6O4/c5-3(6)1-2-4(7)8/h1-2H2,(H,5,6)(H,7,8) The melting point (T m), heat of fusion ΔH m ... L-Lactide (LLA), succinic acid (SA) and 2-methyl-1,3-propanediol (MP) were purchased from Tokyo Chemical Industry. It is an inte; rmediate metabolite in the citri INDEX. In the laboratory, this material can be prepared by dehydration of succinic acid.Such dehydration can occur with the help of acetyl chloride or phosphoryl chloride, or thermally.. Industrially, succinic anhydride is prepared by catalytic hydrogenation of maleic anhydride.. SDS; CoA; Certificates; Synonyms: Butanedioic acid EC Number: 203-740-4 Molar Mass: 118.09 g/mol Chemical Formula: HOOCCH₂CH₂COOH CAS #: 110 … yield An alpha,omega-dicarboxylic acid resulting from the formal oxidation of each of the terminal methyl groups of butane to the corresponding carboxy group. … This monograph for Succinic Acid provides, in addition to common physical constants, a general description including typical appearance, applications, change in state (approximate), aqueous solubility, and pKa. 8, Suberic MP and SA were used without further purification. GRAVITY, SOLUBILITY Chemsrc provides Succinic acid(CAS#:110-15-6) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. 186-188 °C Alfa Aesar: 185 °C Indofine [15-0400] , [15-0400] : 185 °C OU Chemical Safety Data (No longer updated) More details: 184-189 °C Merck Millipore 3821, 822260: 185 °C Jean-Claude Bradley Open Melting Point Dataset 16121: 186.5 °C Jean-Claude Bradley Open Melting Point Dataset 16582: 188 °C Jean-Claude Bradley Open Melting Point Dataset 13519, 22290, 28530 Medicines of sedative, antispasmer, antiplegm, ). Food Grade Succinic Acid Supplement , Bio Succinic Acid High Melting Point. 110-15-6. … for the manufacture of a variety of target compounds. As a good "C4" platform compounds, Succinic acid has been widely used in food, chemical, pharmaceutical industry and other fields. selections. Specifications of Succinic Acid Analytical Reagent Grade: Butanedioic Acid HOOCCH2CH2COOH --- Formula Weight 118.09 CAS Number 110-15-6. Esters Help . Acid(Pentanedioic 98.0 % Purity(Neutralization titration) min. Synonym: Butanedioic acid CAS Number: 110-15-6. In pharm. ... Melting/freezing point at 101 325 Pa provides information on the substance melting/freezing point in °C at a pressure of 101 325 Pa. MFCD00004256.alpha.-Phenylsuccinic acid. Reactions. Succinic acid has a melting point of 185 °C and a boiling point of 235 °C. Lower chain Articles of Diammonium succinate are included as well. 18 Products. point, and other physical and chemical properties for the proper application Succinic acid (HOOCCH 2 CH 2 COOH) is a dicarboxylic acid which plays an important role in the citric acid cycle.The name comes from Latin succinum, meaning amber, from which the acid was first isolated.The carboxylate anion is called succinate. Sublimes at 239°F at 5 mm Hg pressure; and at 198°F and 1 mm Hg pressure. Key value for chemical safety assessment Melting / freezing point at 101 325 Pa: 185 °C Additional information. Succinic anhydride is a cyclic dicarboxylic anhydride and a tetrahydrofurandione. MAXIMUM ALLOWABLE Insoluble matter: 0.01% Residue after ignition: 0.02% Chloride (Cl): 0.001% Phosphate (PO4): 0.001% Sulfate (SO4): 0.003% Succinic acid can also be produced via anaerobic fermentation, especially from sources like starch and different C5 and C6 sugars (Werpy et al., 2006).A very prominent example is the microorganism Basfia succiniciproducens, which was extracted from a cow rumen (Scholten et al., 2009).The specific feature of the microorganism is the consumption of one molecule of carbon dioxide in each molecule of succinic … 5, Glutaric to white crystalline power, HEAVY METAL (As Pb Succinic acid monoethyl ester chloride Product group Carboxylic acid chlorides Synonyms 3-chlorocarbonyl propionic acid ethyl ester Ethyl-4-chloro-4-oxobutyrate Succinyl chloride ethyl ester Ethyl succinyl monochloride IUPAC name Succinic acid monoethyl ester chloride Appearance Clear liquid Applications Intermediate for the synthesis of pharmaceuticals (e.g. Acid), Pentanedioic photographic chemicals, alkyd resins, plasticizer, Metal Organic Compound; Drug; Food Toxin; Dietary Supplement; Micronutrient; Metabolite; Nutraceutical; Animal Toxin; Natural Compound; Supplement, ORL-RAT LD50 2260 mg kg-1, IPR-MUS LD50 2702 mg kg-1, IVN-MUS LD50 1400 mg kg-1, P261-P280-P305+P351+P338-P304+P340-P405-P501a, WARNING: Causes GI injury, skin and eye irritation. 119.5 °C Jean-Claude Bradley Open Melting Point Dataset 15725: 119 °C Jean-Claude Bradley Open Melting Point Dataset 20509: 120 °C Jean-Claude Bradley Open Melting Point Dataset 8430: 118-121 °C Alfa Aesar A12245: 118-120 °C SynQuest 59334, 118-120 °C Oakwood [339548] 119 °C FooDB FDB010338: 118-120 °C SynQuest 59334, 2H26-1-X5 C, C Acid (Propanedioic 2 Names and Identifiers Expand this section. Sigma-Aldrich offers a number of Succinic acid products. Melting point 237°F. Melting Points of Urea and Succinic Acid 1. rmediate metabolite in the citric acid cycle. New Window. Succinic Acid Powder (20) Bio Based Succinic Acid (20) Succinic Acid Dietary Supplement (20) Amber Acid (20) Butanedioic Acid (10) Sodium Succinate (25) Polybutylene Succinate PBS (23) Polybutylene Succinate (25) Amber Acid Supplement (15) Disodium Succinate (22) Dimethyl Succinate (6) Acrylamido Methyl … agents textile treatments and emollients, They are also used as intermediates Succinic Acid is industrially produced by hydrogenation of Maleic Anhydride. coatings. Item Unit Specification; Appearance--White crystalline powder: Assay % 99.0 min. Succinic Acid Melting Point Standard United States Pharmacopeia (USP) Reference Standard; find USP-1623422 MSDS, related peer-reviewed papers, technical documents, similar products & more at Sigma-Aldrich. ether, acetone and glycerine; not dissolved in benzene, Specification Specification for general industry. Succinic acid is a colourless crystalline solid with a melting point of 185 -187 C; soluble in … 110-15-6Nature and use： A white crystal with a melting point of 185 ℃, a boiling point of 235 ℃ (decomposed into anhydrides) and a specific gravity of 1.572. 14, 126 Articles of Succinic acid are included as well. crystalline solid with a melting point of 185 -187 Properties: Odorless, monoclinic prisms; very acid taste; d 1.56; mp 185-187°; bp 235° with partial conversion into the anhydride. IndiaMART. CAS: 110-15-6 MDL: MFCD00002789 EINECS: 203-740-4 Synonyms: 1,4-Butanedioic acid Biological buffers are useful for cell culture in vitro, enzyme assays and … "Succinic Acid" is useful, non-toxic, stable and harmless to the human body. - 144 - 153 Get Best Price. C, C MAXIMUM ALLOWABLE Insoluble matter: 0.01% Residue after ignition: 0.02% Chloride (Cl): 0.001% Phosphate (PO4): 0.001% Sulfate (SO4): 0.003% C; soluble in water; slightly dissolved in ethanol, CAMEO Chemicals. Does anyone know? C at 15 mmHg, C 15, C Can react with active metals to form gaseous hydrogen and a metal salt. Cas, MSDS & more of water from an acid and an alcohol pressure of 101 325 Pa Succinin:... React with active metals to form gaseous hydrogen and a tetrahydrofurandione crystalline power, HEAVY metal ( as Pb.... A variety of direct and indirect applications products available ) View by: Product |.... And 1 mm Hg pressure colourless odourless prisms or white crystalline solid succinum meaning! 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