Description: colorless acicular crystal or white crystal powder. Tasteless, slight special smell. Melting point:132~135℃; Boiling point:228℃(resolve); Flash point: 127℃.Difficultly soluble in water(0.16g/100ml,20℃),soluble in alcohol(1g/10ml),in di
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Classification: 2,4-Hexadienoic acid CAS No.: 110-44-1 Other Names: Sorbic acid MF: C6H8O2 EINECS No.: 203-768-7 Place of Origin: China (Mainl… Appearance:white crystal powder Storage:cool and dry place Package:25kg/bag/carton Application:fo
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Cas:110-44-1
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inquiryAnalysis tests Standard Results Appearance White to yellowish white crystalline powder, has special odor. yellowish white crystalline
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inquiryFood grade preservative powder 2 4-Hexadienoic acid, CAS:110-44-1 Product Description Product Name Sorbic acid
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inquiryProduct description: Product name Sorbic acid CAS number 110-44-1 Assay ≥99% Appearance White crystalline powder Capacity 1000mt/year Application Food, beverage, pickles, tob
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PRODUCT DETAILS Sorbic Acid Chemical Name: Sorbic acid.2,4-di-ethene acid Molecular
Cas:110-44-1
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inquiryIdentification: Chemical Name: Sorbic acid Synonyms: Sorbinsäure; 2,4-Hexadienoic acid; 2-Propenylacrylic acid; Hexa-2,4-dienoic acid CAS No.: 110-44-1 Molecular Formula: C6H8O2 E-Code: E200 Properties: Color less needle cry
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inquiryProduct Name: Sorbic acid MF: C6H8O2 MW: 112.13 EINECS: 203-768-7 Mol File: 110-44-1.mol Sorbic acid Structure Sorbic acid Chemical Properties Melting point 132-135 °C (lit.) Boiling point 228°C density 1.2 g/cm3
integrates independent research and development, production and sales. We have established famous brands at home and abroad. At present, our customers have spread all over the world, we have rich Transportation experience, we aim to serve custome
Sorbic acid CAS:110-44-1 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic intermediates,
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Min.Order:1 Gram
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Type:Lab/Research institutions
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Sorbyl alcohol
sorbic Acid
Conditions | Yield |
---|---|
With Acetobacter aceti MIM2000/28 In phosphate buffer; ethanol for 2h; pH=6.8; | 100% |
sorbic Acid
Conditions | Yield |
---|---|
Stage #1: C12H22O2Si; carbon tetrabromide In methanol at 20℃; for 0.5h; Irradiation; Stage #2: In methanol at 20℃; for 1h; | 98% |
Conditions | Yield |
---|---|
With C4H11FeMo6NO24(3-)*3C16H36N(1+); water; oxygen; sodium carbonate at 50℃; under 760.051 Torr; for 8h; Green chemistry; | 97% |
With 4H3N*4H(1+)*CuMo6O18(OH)6(4-); water; oxygen; sodium carbonate at 50℃; under 760.051 Torr; for 12h; | 95% |
With Acetobacter aceti MIM2000/28 In phosphate buffer; ethanol for 2h; pH=6.8; | 86% |
With sodium hydroxide; triethanolamine; ethylene diamine tetraacetic acid tetrasodium salt Reagens 4:Silber;Leiten von Luft druch ein Gemisch; |
sorbic Acid
Conditions | Yield |
---|---|
Stage #1: C15H28O2Si; carbon tetrabromide In methanol at 20℃; for 0.5h; Irradiation; Stage #2: In methanol at 20℃; for 2.5h; | 92% |
sorbic Acid
Conditions | Yield |
---|---|
Stage #1: C22H26O2Si; carbon tetrabromide In methanol at 20℃; for 0.5h; Irradiation; Stage #2: In methanol at 20℃; for 5h; | 91% |
trans-Crotonaldehyde
(trimethylsilyl)ketene bis(trimethylsilyl) acetal
sorbic Acid
Conditions | Yield |
---|---|
With zinc dibromide In tetrahydrofuran for 3h; Ambient temperature; | 85% |
(E)-2-(Toluene-4-sulfonyloxy)-hex-4-enoic acid
sorbic Acid
Conditions | Yield |
---|---|
With potassium tert-butylate In dimethyl sulfoxide at 25 - 30℃; for 1h; | 81% |
Conditions | Yield |
---|---|
With pyridine Heating; | 80% |
sorbic Acid
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene In acetonitrile at 20℃; | 77% |
4-hydroxy-6-methyl-tetrahydro-2H-pyran-2-one
sorbic Acid
Conditions | Yield |
---|---|
Amberlyst-70 In tetrahydrofuran; water at 169.84℃; under 15514.9 Torr; for 12h; Product distribution / selectivity; Inert atmosphere; | 64.1% |
A
sorbic Acid
B
β-Amino-propionamidin
Conditions | Yield |
---|---|
With hydrogenchloride for 6h; Heating; | A 15% B n/a C n/a |
Conditions | Yield |
---|---|
With toluene; zinc bis(3-methylbutanoate) Erhitzen des dabei erhaltenen Reaktionsprodukts mit wenig Natriumhydroxid in Diaethylenglykol; | |
With zinc disorbate Erhitzen des Reaktionsprodukts mit wss.Natronlauge; | |
With toluene; zinc bis(3-methylbutanoate) Erhitzen des dabei erhaltenen Reaktionsprodukts ohne Zusatz auf 205grad; | |
With toluene; zinc bis(3-methylbutanoate) Erhitzen des dabei erhaltenen Reaktionsprodukts mit wss.Natronlauge und anschliessend mit wss.Schwefelsaeure; |
tetrachloromethane
N-Bromosuccinimide
6-methyl-2-oxo-tetrahydro-pyran-3-carboxylic acid ethyl ester
sorbic Acid
Conditions | Yield |
---|---|
Erhitzen des mit N,N-Diaethyl-anilin auf 140grad und Erhitzen des Reaktionsprodukts mit wss. Natronlauge; |
6-methyl-2-oxo-tetrahydro-pyran-3-carboxylic acid ethyl ester
sorbic Acid
Conditions | Yield |
---|---|
With tetrachloromethane; N-Bromosuccinimide Erhitzen des Reaktionsprodukts mit N,N-Diaethyl-anilin auf 140grad und Erhitzen des erhaltenen Sorbinsaeure-aethylesters mit wss.Natronlauge; |
Conditions | Yield |
---|---|
at 140℃; Erhitzen des Reaktionsprodukts mit wss. Natronlauge; |
(2Z)-2,5-hexadienoic acid
sorbic Acid
Conditions | Yield |
---|---|
With alkaline solution |
hex-4-ynoic acid
sorbic Acid
Conditions | Yield |
---|---|
With potassium hydroxide; ethylene glycol at 160℃; |
Conditions | Yield |
---|---|
at 145℃; |
(but-2-enylidene)malonic acid
A
sorbic Acid
B
methylammonium carbonate
sorbic Acid
Conditions | Yield |
---|---|
bei der Kalischmelze; |
Conditions | Yield |
---|---|
With zinc(II) chloride at 50 - 60℃; und Destillation des Reaktionsprodukts unter vermindertem Druck; | |
With boron trioxide; diethyl ether; oxalic acid at -15 - 15℃; und Erwaermen des Reaktionsprodukts mit 35prozentiger H2SO4 auf 70-80grad; | |
With boron trioxide; diethyl ether; salicylic acid at -15 - 15℃; und Erwaermen des Reaktionsprodukts mit 35prozentiger H2SO4 auf 70-80grad; |
trans-Crotonaldehyde
malonic acid
A
sorbic Acid
B
(2Z,4E)-hexa-2,4-dienoic acid
Conditions | Yield |
---|---|
With pyridine at 98℃; for 1h; Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
(but-2-enylidene)malonic acid
A
sorbic Acid
B
(2Z,4E)-hexa-2,4-dienoic acid
Conditions | Yield |
---|---|
With pyridine at 100℃; for 3h; Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
Conditions | Yield |
---|---|
With thionyl chloride In N,N-dimethyl-formamide for 0.666667h; Heating; | 100% |
With thionyl chloride; N,N-dimethyl-formamide at 80℃; for 0.666667h; Inert atmosphere; | 98% |
With thionyl chloride In N,N-dimethyl-formamide at 80℃; for 0.666667h; Inert atmosphere; | 98% |
sorbic Acid
(E)-3,5-hexadienoic acid
Conditions | Yield |
---|---|
With lithium diisopropyl amide for 1h; Ambient temperature; | 100% |
With lithium diisopropyl amide In tetrahydrofuran for 1h; Ambient temperature; | 100% |
With n-butyllithium; diisopropylamine In tetrahydrofuran at -10 - 20℃; for 1h; | 98% |
styrene
sorbic Acid
hexanal
(1RS,2SR)-2-(1-hydroxyhexyl)-3,5-hexadienoic acid
Conditions | Yield |
---|---|
In tetrahydrofuran; water; diisopropylamine; pentane | 100% |
sorbic Acid
1-hydroxy-pyrrolidine-2,5-dione
(2E,4E)-2,5-dioxopyrrolidin-1-yl hexa-2,4-dienoate
Conditions | Yield |
---|---|
With dicyclohexyl-carbodiimide In tetrahydrofuran for 2.5h; Inert atmosphere; | 100% |
sorbic Acid
Conditions | Yield |
---|---|
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 1.5h; | 100% |
Conditions | Yield |
---|---|
With thionyl chloride at -10℃; for 2h; Reflux; Inert atmosphere; | 99% |
With chloro-trimethyl-silane In dichloromethane for 16h; | 99% |
Stage #1: sorbic Acid With oxalyl dichloride In dichloromethane; N,N-dimethyl-formamide at 0℃; for 1h; Inert atmosphere; Stage #2: methanol In dichloromethane; N,N-dimethyl-formamide at 0 - 20℃; | 95% |
sorbic Acid
(+)-(1S,2R,5R)-isomenthol
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane for 3h; Ambient temperature; | 99% |
Conditions | Yield |
---|---|
tetrachlorobis(tetrahydrofuran)hafnium(IV) In benzene for 38h; Heating; | 99% |
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; for 12.0833h; | 94% |
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane for 48h; | 90% |
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane for 48h; | 90% |
With mineral acid Heating; | 40.2% |
sorbic Acid
Conditions | Yield |
---|---|
Stage #1: Wang resin-bound Fmoc-L-Tyr(t-Bu) With piperidine In N,N-dimethyl-formamide at 20℃; Stage #2: sorbic Acid With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine In N,N-dimethyl acetamide at 20℃; for 18h; Stage #3: With trifluoroacetic acid In dichloromethane at 20℃; for 18h; | 99% |
sorbic Acid
(6S,7S,12S,E)-6-hydroxy-12-isopropyl-7,9-dimethyloxacyclododec-9-en-2-one
(6S,7S,12S,E)-12-isopropyl-7,9-dimethyl-2-oxooxacyclododec-9-en-6-yl 4,15-dioxo-19-(2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)-8,11-dioxa-5,14-diazanonadecan-1-oate
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 15h; Höfle-Steglich esterification; | 99% |
sorbic Acid
Conditions | Yield |
---|---|
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 1.5h; | 99% |
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; Inert atmosphere; | 99% |
sorbic Acid
methyl 10-hydroxydecanoate
methyl 10-((2E,4E)-hexa-2,4-dienoyloxy)decanoate
Conditions | Yield |
---|---|
Stage #1: sorbic Acid With 2,4,6-trichlorobenzoyl chloride; triethylamine In dichloromethane at 20℃; Yamaguchi reaction; Cooling with ice; Stage #2: methyl 10-hydroxydecanoate With dmap In dichloromethane at 20℃; Yamaguchi reaction; | 98% |
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; | 98% |
sorbic Acid
Sorbyl alcohol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether for 1h; Heating; | 97% |
Stage #1: sorbic Acid With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 0.5h; Stage #2: With sodium tetrahydroborate; water In tetrahydrofuran at 0℃; for 0.5h; | 75% |
With strain of the zygomycete fungus S. racemosum MUT 770 In dimethyl sulfoxide for 72h; Enzymatic reaction; | 74% |
sorbic Acid
(2S,3R)-2-((2E,4E)-Hexa-2,4-dienoylamino)-3-hydroxy-butyric acid tert-butyl ester
(2E,4E)-Hexa-2,4-dienoic acid (1R,2S)-2-tert-butoxycarbonyl-2-((2E,4E)-hexa-2,4-dienoylamino)-1-methyl-ethyl ester
Conditions | Yield |
---|---|
With dmap; 4-(dimethylamino)pyridine hydrochloride; dacarbazine In dichloromethane at 20℃; for 6h; | 97% |
sorbic Acid
aluminum isopropoxide
aluminium(III) sorbate bis(isopropoxide)
Conditions | Yield |
---|---|
In benzene byproducts: isoprpopanol; to Al(OCH(CH3)2)3 in benzene was added acid (molar ratio 1:1), mixt. was heated under reflux; i-PrOH was fractionated, solvent was removed under reduced pressure; elem. anal.; | 97% |
sorbic Acid
(E)-3-(4-Methoxy-7-methyl-bicyclo[4.2.0]octa-1(6),2,4-trien-7-yl)-but-2-en-1-ol
(2E,4E)-Hexa-2,4-dienoic acid (E)-3-(4-methoxy-7-methyl-bicyclo[4.2.0]octa-1(6),2,4-trien-7-yl)-but-2-enyl ester
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide | 96% |
sorbic Acid
O-methylresorcine
3-methoxyphenyl (2E,4E)-2,4-hexanedienoate
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 24h; | 96% |
sorbic Acid
(2S,3R)-2-((2E,4E)-Hexa-2,4-dienoylamino)-3-hydroxy-butyric acid tert-butyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 5h; | 96% |
Conditions | Yield |
---|---|
In benzene byproducts: isoprpopanol; to Al(OCH(CH3)2)3 in benzene was added acid (molar ratio 1:2), mixt. was heated under reflux; i-PrOH was fractionated, solvent was removed under reduced pressure; elem. anal.; | 96% |
sorbic Acid
Conditions | Yield |
---|---|
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 1.5h; | 96% |
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; Inert atmosphere; | 96% |
Conditions | Yield |
---|---|
Stage #1: sorbic Acid With thionyl chloride In methanol at 0℃; for 3h; Reflux; Inert atmosphere; Stage #2: Inert atmosphere; | 95% |
Multi-step reaction with 2 steps 1: phosphorus pentachloride / man fraktioniert das Produkt im Vakuum View Scheme |
Conditions | Yield |
---|---|
Stage #1: sorbic Acid With 4-(dimethylamino)pyridine N-oxide; phenylboronic acid In fluorobenzene at 20℃; for 0.0833333h; Molecular sieve; Reflux; Stage #2: phenethylamine In fluorobenzene for 16h; Molecular sieve; Reflux; | 95% |
sorbic Acid
Conditions | Yield |
---|---|
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 1.5h; | 95% |
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