Soluble in alcohol, methanol, colourless odourless prisms or white crystalline powder. in intermediary metabolism (Krebs cycle) in the body. The full spectrum can only be viewed using a FREE account. Acid (Butanedioic Acid) is a dicarboxylic
C(CC(=O)O)C(=O)O
Related Products. New Window. Acid(Heptanedioic Acid), 105
Colorless
More>> Succinic acid for synthesis. 8, Suberic
CAS Number: 110-15-6 EINECS EC Number: 203-740-4 Molecular Formula: HOOCCH2CH2COOH Molecular Weight: 118.09 Relevant uses and uses advised against (if any): Industrial Manufacturing. … rmediate metabolite in the citric acid cycle. Succinic acid CAS No. 110-15-6 Molecular formula C4H6O4 Molecular Weight 118.09 Appearance colorless to white crystal or white crystal powder Purity ≥ 99.5% Melting range 184.0~187.0°C Chloride ≤ 0.007% Sulphate (SO42-) Linear Formula: HOOCCH 2 CH 2 COOH. There are almost
The excess alkene is removed by distillation in vacuo, the resulting alkenyl succinic anhydride hydrolyzed with dilute sodium hydroxide solution and the disodium salt reacted with an acid to achieve an alkenebutanedioic acid. Succinic anhydride appears as colorless needles or white crystalline solid. 3.2.3 Melting Point. It is soluble in water and slightly soluble in ethanol for the preparation of pentaheterocyclic compounds.Specification:Test ItemsSp Articles of 2-Dodecen-1-yl succinic anhydride are included as well. Near Me. Physical: Vapor-phase succinic acid is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals; the half-life for this reaction in air is estimated to be about 5.8 days. Product Name & Other Names: Succinic Acid or Butanedioic acid. … infinite esters obtained from carboxylic
110-15-6. … Properties: Odorless, monoclinic prisms; very acid taste; d 1.56; mp 185-187°; bp 235° with partial conversion into the anhydride. - 110 C, C
2 Names and Identifiers Expand this section. Carboxylic acid
Help . Melting Point ℃ 185 min. 12, 128
DESCRIPTION. are formed by removal of water from an acid and an alcohol. Melting point 237°F. SECTION 1. Less<< Succinic acid MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents. coupling agents. - 106
- 134
(-)-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. compounds, Intermediate for dyes, perfumes, lacquers,
It does not dissolve in benzene, carbon sulfide, carbon tetrachloride or oil ether. CAS number. C, C
: 110-15-6 1.2 Relevant identified uses of the substance or mixture and uses advised against Identified uses : Laboratorychemicals, Industrial & for professional use only. Acid), 95
CopyCopied, CSID:1078, http://www.chemspider.com/Chemical-Structure.1078.html (accessed 23:41, Jan 7, 2021)
Succinic acid - cas 110-15-6, synthesis, structure, density, melting point, boiling point Human Metabolome Database (HMDB)-21 °C.
An alpha,omega-dicarboxylic acid resulting from the formal oxidation of each of the terminal methyl groups of butane to the corresponding carboxy group. agriculture, and food products, and other industrial
acid of four carbon atoms. acids. Insoluble Solubility in chloroform: Soluble Related compounds Related Monomers. MAXIMUM ALLOWABLE Insoluble matter: 0.01% Residue after ignition: 0.02% Chloride (Cl): 0.001% Phosphate (PO4): 0.001% Sulfate (SO4): 0.003% IndiaMART > Pharma Ingredients & Raw Materials > API Intermediate > Succinic Acid. MP of succinic acid is 188-190 C and MP of adipic acid is 152-154 C. I would think adipic acid has a higher melting point due to its higher molar mass, but this is … melting point” quickly, and then repeat with more care for a more precise reading. DL-Phenylsuccinic acid, 98+% alpha-Phenylsuccinic acid (S)-2-Phenylsuccinicacid. In pharm. 98.0 % Purity(Neutralization titration) min. esters are used as in a variety of direct and indirect applications. 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. Succinic acid is a kind of common natural organic acid, due to it’s from amber distilled in 1550 for the first time, so the Succinic acid is also known as Amber acid. Stable. Point, Boiling
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. 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 … New Window. photographic chemicals, alkyd resins, plasticizer, Metal
Location. Molecular Weight: 118.09 . Succinic acid is a dicarboxylic acid with the chemical formula (CH2)2(CO2H)2. Does anyone know? Under these conditions, it is possible to substitute succinic acid for its anhydride obtaining the same results. SPECIFICATION, FUMARIC
point, and other physical and chemical properties for the proper application
Preparation. C, 230
Sigma-Aldrich offers a number of Succinic acid products. - 128 C, C
industry, succinic acid high grade is used in the production of synthetic tranquilizer, contraceptive, cancer drugs, etc. Succinic acid can also be used as analytical reagent and flavoring agents. Acid). It does not dissolve in benzene, carbon sulfide, carbon tetrachloride or oil ether. The succinein has been obtained … Environmental: Succinic acid is not expected to volatilize from water surfaces. antiphogistic, anrhoter, contraception and cancer-curing. It derives from a succinic acid. Contents. 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. #, Melting
- 126 C, C
1 Structures Expand this section. MFCD00004256.alpha.-Phenylsuccinic acid. Packing: in 25kg bags It is a diprotic acid. Succinic acid is a colorless crystalline solid with a melting point of 185-187° C. It is soluble in water, slightly dissolves in ethanol, ether, acetone and glycerine. length (Straight), CAS
"Succinic Acid" is useful, non-toxic, stable and harmless to the human body. C at 15 mmHg, C
... Melting/freezing point at 101 325 Pa provides information on the substance melting/freezing point in °C at a pressure of 101 325 Pa. C, 302
C at 15 mmHg, C
soluble, REFRACTIVE
Succinic Acid CAS NO. Succinic Acid (75 products available) View by: Product | Supplier. Information on Registered Substances comes from registration dossiers which have been assigned a registration number. - 190 C, 235
0.11 M. EPA . acid, arboxylic acid can
One gram dissolves in 13 ml cold water, 1 ml boiling water, 18.5 ml alcohol, 6.3 ml methanol, 36 ml acetone, 20 ml glycerol, 113 ml ether. 2; Flammability: 1; Reactivity: 0, SALES
The carboxylate anion is called succinate and esters of succinic acid are called alkyl succinates. Acid(Pentanedioic
amides, and nitriles for the application of drug,
esters are used as flavouring base materials, plasticizers, solvent carriers and
The melting temperature of succinic acid is 185 - 187 °C. 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 … New Window-21.0 °C. Phenylsuccinate. Chemsrc provides Succinic acid(CAS#:110-15-6) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Combustible. Help. for the manufacture of a variety of target compounds. - 191
Butanedioic acid, phenyl-Succinic acid, phenyl-2-Phenylsuccinate. & MALEIC ACID, GENERAL
The common method of synthesis of succinic acid is the
Specifications of Succinic Acid Analytical Reagent Grade: Butanedioic Acid HOOCCH2CH2COOH --- Formula Weight 118.09 CAS Number 110-15-6. Help. Other names. 19.1 mg/mL at 25 °C. Acid), Pentanedioic
Succinic Acid of NIPPON SHOKUBAI has not only been used as food additives but also biodegradable polymers, bath additives, plating agents, photochemicals and so on. Physical: Vapor-phase succinic acid is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals; the half-life for this reaction in air is estimated to be about 5.8 days. Download MSDS File. An
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