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Min.Order:1 Kilogram
Negotiable
Type:Manufacturers
inquiryDayangChem exported this product to many countries and regions at best price in China. If you are looking for the product’s supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product specifica
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inquiryOur main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block
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Type:Manufacturers
inquiryTianfu Chemical, built in 2009, is a professional supplier for API materials in China. With 10 years development, we have bulit our own factory and lab to produce a certain of products. And we have established stable business relationship
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Min.Order:1 Kilogram
FOB Price: $139.0 / 210.0
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inquiryAppearance:White to off-white powder Storage:room temperature Package:25kg/drum Application:chemicals Transportation:Express/Sea/Air Port:any port in china
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryDL-3-Aminoisobutyric acid CAS:10569-72-9 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
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Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
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Min.Order:1 Kilogram
Negotiable
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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
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inquiryA substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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inquiryZibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
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inquiryThe above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providing h
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Min.Order:1 Gram
Negotiable
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inquiryfactory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
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inquiryShandong Mopai Biotechnology Co., LTD is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemicals. W
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Min.Order:1 Gram
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inquiryHigh quality,stable supply chain.Appearance:white/off-white or light yellow Storage:Store in cool and dry place, keep away from strong light and heat. Package:aluminum bottle,glass bottle,PTFE bottle,cardboard drum Application:This product can be use
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inquiryWe are a Union of chemistry in China, consists of chemists,engineers, laboratories,factories in China. We organize surplus capacity of R&D and production as well as custom synthesis for chemical products and chemical business project. We are supp
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inquiryhigh purity,in stock Package:25kg/drum,or as per customers'demand Application:API,or Intermediates,fine chemicals Transportation:air,sea,courier
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inquiryTAIHO Unique Advantages:1.We're factory2.Free samples available3.Commodity inspection can be done4.ISO9001,Kosher certifications5.10 years experiences Storage:Store in cool &dry place Package:aluminium foil bag/fiber can/plastic drum Application:comp
BOC Sciences provides a wide range of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell. https://aapep.bocsci.com/product/dl-
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Min.Order:1 Gram
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inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
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inquiryDL-3-Aminoisobutyric acid Application:DL-3-Aminoisobutyric acid
Supply top quality products with a reasonable price Application:api
5,6-dihydrothymine
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
With phosphoric acid; dihydropyrimidinase; N-carbamoyl- -alanine amidohydrolase; nickel dichloride In aq. phosphate buffer at 30℃; pH=8; Enzymatic reaction; |
2-benzyl-4-methylisoxazolidin-5-one
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
With palladium on activated charcoal; hydrogen In 1,4-dioxane; water at 85℃; for 16h; | 95% |
4-methyl-N-(S)-1-phenylethylisoxazolidin-5-one
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
With palladium on activated charcoal; hydrogen In 1,4-dioxane; water at 85℃; for 16h; | 87% |
trans-1-benzoyl-2-tert-butyl-3,5-dimethylperhydropyrimidin-4-one
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
With hydrogenchloride at 180℃; for 8h; | 69% |
2-methyl-3-benzylaminopropanoic acid
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethanol | |
With hydrogen; PdCl2/C In acetic acid |
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
With ammonium formate; palladium on activated charcoal In tetrahydrofuran; methanol |
B
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
With naphthalene; sodium In 1,2-dimethoxyethane at -78℃; for 0.5h; | A 31 mg B n/a |
B
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
With naphthalene; sodium In 1,2-dimethoxyethane at -78℃; for 0.5h; | A 67 mg B n/a |
ethyl 2-cyanopropionate
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
With sulfuric acid; acetic acid; platinum Hydrogenation.wiederholtes Eindampfen des Reaktionsprodukts mit Wasser; |
N,N,O-Tris-(trimethylsilyl)-β-aminoisobuttersaeure
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
With water; triethylamine In tetrahydrofuran; pentane at 20℃; |
methyl methacrylate
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
With ethanol; ammonia; water; hydroquinone at 125 - 130℃; und Erwaermen des Reaktionsprodukts mit wss.HCl; |
β-amino-α-methyl propionic acid methyl ester
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
With lithium hydroxide In water |
A
DL-3-aminoisobutyric acid
B
α-aminoacrylic acid
C
2-amino-4-hydroxypentanedioic acid
Conditions | Yield |
---|---|
With hydrogenchloride at 110℃; for 17h; Hydrolysis; |
formamide
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
With Canyon Diablo iron meteorites at 140℃; for 24h; Reagent/catalyst; Temperature; |
methacrylonitrile
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
With sulfuric acid; sulfur trioxide |
propylamine
formic acid
A
DL-3-aminoisobutyric acid
B
rac-Ala-OH
C
2-aminobutanoic acid
D
4-amino-n-butyric acid
Conditions | Yield |
---|---|
In water at 10 - 20℃; for 1h; contact glow discharge electrolysis (500-600 V, 45 mA); Further byproducts given; | A 9.8% B 3.4% C 0.9% D 8.1% |
propylamine
formic acid
A
DL-3-aminoisobutyric acid
B
2-aminobutanoic acid
C
3-amino propanoic acid
D
4-amino-n-butyric acid
Conditions | Yield |
---|---|
In water at 10 - 20℃; for 1h; contact glow discharge electrolysis (500-600 V, 45 mA); Further byproducts given; | A 9.8% B 0.9% C 3.4% D 8.1% |
Sodium; 2-methyl-3-ureido-propionate
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
With hydrogen cation Yield given; |
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
With hydrogen iodide; acetic acid |
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
With water wiederholtes Eindampfen; |
(benzoylamino-methyl)-methyl-malonic acid diethyl ester
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
With hydrogen bromide |
methacrylic acid methyl ester
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
(i) NH3, MeOH, (ii) aq. HCl; Multistep reaction; |
formic acid
1-amino-2-propene
A
propylamine
B
DL-3-aminoisobutyric acid
C
glycine
D
3-amino propanoic acid
E
4-amino-n-butyric acid
Conditions | Yield |
---|---|
With hydrogen; oxygen In water for 3h; Product distribution; various unsaturated amines; investigation of the direct carboxylation of C=C bond, the effect of formic acid concentration as well as the flame composition on product(s); radical mechanism is proposed; | A n/a B 38% C n/a D n/a E 5% |
2-cyanopropanoic acid
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
Hydrogenation; |
sulfuric acid
ethyl 2-cyanopropionate
acetic acid
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
beim folgenden Verseifen.Hydrogenation; |
propylamine
formic acid
A
DL-3-aminoisobutyric acid
B
glycine
C
2-aminobutanoic acid
D
3-amino propanoic acid
E
4-amino-n-butyric acid
Conditions | Yield |
---|---|
In water at 10 - 20℃; for 1h; Product distribution; contact glow discharge electrolysis; variation of pH, effect of time; | A 9.8% B 0.2% C 0.9% D 3.4% E 8.1% |
Conditions | Yield |
---|---|
With hydrogen azide for 5h; Quantum yield; Ambient temperature; Irradiation; |
Conditions | Yield |
---|---|
With hydrogenchloride | 100% |
With thionyl chloride for 4.5h; | 85% |
Stage #1: ethanol; DL-3-aminoisobutyric acid With thionyl chloride at 0 - 90℃; for 6h; Stage #2: With ammonium hydroxide In dichloromethane at 20℃; for 2h; |
methanol
DL-3-aminoisobutyric acid
β-amino-α-methyl propionic acid methyl ester
Conditions | Yield |
---|---|
With thionyl chloride at 20℃; | 100% |
With thionyl chloride for 3h; Reflux; | |
With thionyl chloride at 0 - 20℃; |
DL-3-aminoisobutyric acid
3-amino-2-methylpropan-1-ol hydrochloride
Conditions | Yield |
---|---|
Stage #1: DL-3-aminoisobutyric acid With borane-THF In tetrahydrofuran at 20℃; for 20.5h; Reflux; Stage #2: With hydrogenchloride In 1,4-dioxane; diethyl ether for 0.333333h; | 100% |
DL-3-aminoisobutyric acid
di-tert-butyl dicarbonate
N-tert-butoxycarbonyl-3-amino-2(RS)-methylpropionic acid
Conditions | Yield |
---|---|
With sodium hydroxide; tert-butyl alcohol In water at 30℃; for 18h; | 99% |
With sodium hydroxide In tetrahydrofuran at 20 - 30℃; for 18h; | 97% |
Stage #1: DL-3-aminoisobutyric acid; di-tert-butyl dicarbonate With sodium hydroxide In 1,4-dioxane; water at 5℃; for 0.916667h; Stage #2: With hydrogenchloride In 1,4-dioxane; water | 96% |
DL-3-aminoisobutyric acid
1-chloro-2,6-dinitrobenzene
3-(2,6-Dinitro-phenylamino)-2-methyl-propionic acid
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In ethanol for 6h; Heating; | 98% |
DL-3-aminoisobutyric acid
3,5-dichlorobenzoyl chloride
Conditions | Yield |
---|---|
With sodium hydroxide In water for 1h; | 93% |
methanol
DL-3-aminoisobutyric acid
β-aminoisobutyric acid methyl ester hydrochloride
Conditions | Yield |
---|---|
With thionyl chloride at 0 - 20℃; for 6h; | 90% |
With trimethylsilyl isocyanate at 0 - 20℃; for 48h; Inert atmosphere; | 75% |
With thionyl chloride at -10℃; for 1h; Heating / reflux; | |
With thionyl chloride at 0℃; for 18h; Inert atmosphere; Reflux; |
Conditions | Yield |
---|---|
Stage #1: formaldehyd; DL-3-aminoisobutyric acid With trifluoroacetic acid at 150℃; for 0.0833333h; Sealed tube; Inert atmosphere; Microwave irradiation; Stage #2: With sulfuric acid In methanol for 4h; Reflux; | 90% |
DL-3-aminoisobutyric acid
(1S)-(-)-camphanic chloride
(2RS)-3-camphanoylamino-2-methylpropanoic acid
Conditions | Yield |
---|---|
With sodium hydroxide In water; toluene for 3h; | 89% |
DL-3-aminoisobutyric acid
3-methyl-2-azetidinone
Conditions | Yield |
---|---|
With sulfenamide (5); triphenylphosphine In acetonitrile at 80℃; for 2h; | 89% |
With tris(2-oxo-3-oxazolinyl)phosphine oxide; triethylamine In acetonitrile for 6h; Heating; | 75% |
With tris(1,3-dihydro-2-oxobenzoxazolin-3-yl) phosphine oxide; triethylamine In acetonitrile for 6h; Heating; | 71% |
With 2-chloro-1-methyl-pyridinium iodide; triethylamine In acetonitrile for 2h; Heating; | 57% |
DL-3-aminoisobutyric acid
tert-butylisonitrile
phenylacetaldehyde
Conditions | Yield |
---|---|
Stage #1: DL-3-aminoisobutyric acid; phenylacetaldehyde In water at 20℃; Stage #2: tert-butylisonitrile In water at 20℃; Ugi reaction; | 88% |
In methanol for 24h; Ambient temperature; |
DL-3-aminoisobutyric acid
Benzyl isocyanide
propionaldehyde
Conditions | Yield |
---|---|
Stage #1: DL-3-aminoisobutyric acid; propionaldehyde In water at 20℃; Stage #2: Benzyl isocyanide In water at 20℃; Ugi reaction; | 84% |
DL-3-aminoisobutyric acid
tert-butylisonitrile
isobutyraldehyde
Conditions | Yield |
---|---|
Stage #1: DL-3-aminoisobutyric acid; isobutyraldehyde In water at 20℃; Stage #2: tert-butylisonitrile In water at 20℃; Ugi reaction; | 82% |
DL-3-aminoisobutyric acid
Benzyl isocyanide
isobutyraldehyde
Conditions | Yield |
---|---|
Stage #1: DL-3-aminoisobutyric acid; isobutyraldehyde In water at 20℃; Stage #2: Benzyl isocyanide In water at 20℃; Ugi reaction; | 82% |
DL-3-aminoisobutyric acid
Benzyl isocyanide
isovaleraldehyde
Conditions | Yield |
---|---|
Stage #1: DL-3-aminoisobutyric acid; isovaleraldehyde In water at 20℃; Stage #2: Benzyl isocyanide In water at 20℃; Ugi reaction; | 82% |
DL-3-aminoisobutyric acid
tert-butylisonitrile
isovaleraldehyde
Conditions | Yield |
---|---|
Stage #1: DL-3-aminoisobutyric acid; isovaleraldehyde In water at 20℃; Stage #2: tert-butylisonitrile In water at 20℃; Ugi reaction; | 81% |
DL-3-aminoisobutyric acid
2-methoxy-5-methylphenyl isocyanate
3-(3-(2-methoxy-5-methylphenyl)ureido)-2-methylpropanoic acid
Conditions | Yield |
---|---|
In methanol at 20℃; | 81% |
DL-3-aminoisobutyric acid
ethyl trifluoroacetate,
2-methyl-3-(2,2,2-trifluoroacetamido)propanoic acid
Conditions | Yield |
---|---|
Stage #1: DL-3-aminoisobutyric acid With triethylamine In methanol for 0.0833333h; Stage #2: ethyl trifluoroacetate, In methanol for 24h; | 81% |
methanol
DL-3-aminoisobutyric acid
[di(propan-2-yl)amino](oxo)acetyl chloride
Conditions | Yield |
---|---|
Stage #1: methanol; DL-3-aminoisobutyric acid With thionyl chloride at 0 - 20℃; Stage #2: [di(propan-2-yl)amino](oxo)acetyl chloride With triethylamine In dichloromethane at 0 - 20℃; for 6h; | 78% |
2,5-dimethylphenyl isocyanate
DL-3-aminoisobutyric acid
3-(3-(2,5-dimethylphenyl)ureido)-2-methylpropanoic acid
Conditions | Yield |
---|---|
In methanol at 20℃; | 76% |
iodobenzene
DL-3-aminoisobutyric acid
N-phenyl-3-aminoisobutyric acid
Conditions | Yield |
---|---|
With potassium phosphate; copper(I) bromide; 1,1'-bi-2-naphthol In N,N-dimethyl-formamide at 40℃; for 10h; | 72% |
phthalic anhydride
DL-3-aminoisobutyric acid
3-(1,3-dioxoisoindolin-2-yl)-2-methylpropanoic acid
Conditions | Yield |
---|---|
With triethylamine In toluene Reflux; | 70% |
DL-3-aminoisobutyric acid
Conditions | Yield |
---|---|
With copper(l) iodide; caesium carbonate In water; N,N-dimethyl-formamide at 150℃; for 4h; Microwave irradiation; | 70% |
DL-3-aminoisobutyric acid
2,2,2-Trichloroethyl chloroformate
2-methyl-3-((2,2,2-trichloroethoxy)carbonylamino)propanoic acid
Conditions | Yield |
---|---|
With sodium hydroxide In water at 0 - 20℃; for 2.5h; | 68% |
DL-3-aminoisobutyric acid
4-chloro-2-isocyanato-1-methylbenzene
3-(3-(5-chloro-2-methylphenyl)ureido)-2-methylpropanoic acid
Conditions | Yield |
---|---|
In methanol at 20℃; | 61% |
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