2-AMINOCAPRIC ACID

Product Name: 2-AMINOCAPRIC ACID
CAS No.: 17702-88-4
Chemical Name: 2-AMINOCAPRIC ACID
Synonyms: DL-decyline [;2-AMINOCAPRIC ACID;D-2-Aminocapric acid;2-AMINODECANOIC ACID;REF DUPL: DL-decyline;Decanoic acid, 2-amino-;2-Aminodecanoicacidpurum;D,L 2-AMINODECANOIC ACID;(R)-2-Aminodecanoic acid;(-)-D-2-Aminocapric acid
CBNumber: CB4121343
Molecular Formula: C10H21NO2
Formula Weight: 187.28
MOL File: 17702-88-4.mol

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2-AMINOCAPRIC ACID Property

Melting point:: ~262 °C (dec.)
Boiling point:: 300.9±25.0 °C(Predicted)
Density: 0.973±0.06 g/cm3(Predicted)
storage temp.: Keep in dark place,Inert atmosphere,Room temperature
pka: 2.55±0.24(Predicted)

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Safety

WGK Germany: 3

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Biosynth Carbosynth

Product number: FA148981
Product name: 2-Aminodecanoicacid
Packaging: 25mg
Price: $59
Updated: 2021/12/16

Biosynth Carbosynth

Product number: FA148981
Product name: 2-Aminodecanoicacid
Packaging: 50mg
Price: $103
Updated: 2021/12/16

Biosynth Carbosynth

Product number: FA148981
Product name: 2-Aminodecanoicacid
Packaging: 100mg
Price: $179
Updated: 2021/12/16

Activate Scientific

Product number: AS87173
Product name: 2-Aminodecanoic acid
Purity: 95+%
Packaging: 250mg
Price: $210
Updated: 2021/12/16

AK Scientific

Product number: X5391
Product name: 2-Aminodecanoicacid
Packaging: 100mg
Price: $212
Updated: 2021/12/16

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2-AMINOCAPRIC ACID Chemical Properties,Usage,Production

Synthesis

773837-37-9

124-19-6

17702-88-4

GENERAL METHOD: Acetylacetonate dicarbonylrhodium (Rh(acac)(CO)2, 2.6 mg, 0.01 mmol) and xantphos (28.9 mg, 0.05 mmol) were placed in an autoclave according to the typical method described above. Subsequently, a solution of 1,2-dimethoxyethane (DME, 8 mL) of olefin (5 mmol) was added through a cannula. The autoclave was pressurized with a 20 bar carbon monoxide/hydrogen (1:1 molar ratio) mixture and the reaction was stirred for 18 h at 80 °C. Upon completion of the reaction, the reactor was cooled to room temperature, an aqueous solution (2 mL) of ammonium chloride (NH4Cl, 5.5 mmol) and sodium cyanide (NaCN, 5.5 mmol) was added through the inlet cannula, and the reaction was continued for another 20 hours at 50 °C. After post-processing and purification, the resulting α-aminonitrile (4.1 mmol) was suspended in concentrated hydrochloric acid solution and stirred at 40 °C for 6 h. The product was then dissolved in methanol. The product was dissolved in methanol and the solvent was evaporated after adjusting the pH to the isoelectric point with ammonia (aq) to finally obtain the target amino acid 2-aminodecanoic acid.

References

[1] Tetrahedron, 2017, vol. 73, # 17, p. 2389 - 2395

2-AMINOCAPRIC ACID Preparation Products And Raw materials

Raw materials

Preparation Products

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2-AMINOCAPRIC ACID Suppliers

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17702-88-4, 2-AMINOCAPRIC ACIDRelated Search:

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2-AMINOCAPRIC ACID

2-AMINODECANOIC ACID

2-Aminodecanoicacidpurum

DL-decyline [

2-AMINODECANOIC ACID PURUM 97%

(-)-D-2-Aminocapric acid

(R)-2-Aminodecanoic acid

D,L 2-AMINODECANOIC ACID

[R,(-)]-2-Aminocapric acid

[R,(-)]-2-Aminodecanoic acid

D-2-Aminocapric acid

REF DUPL: DL-decyline

DL-decyline 2-AMinodecanoic acid

Decanoic acid, 2-amino-

17702-88-4

Linear Core Amino Acids

Peptide Synthesis

Specialty Synthesis

Unnatural Amino Acid Derivatives