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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

Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
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info@hanhongsci.com
Country
China
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42934
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+86 (21) 6435-5022
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China
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65
Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Fax
010-65763397
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waley188@sohu.com
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China
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12335
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Shanghai PharmOrgsyn Technology Co., LTD.
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021-+86-021-38228826 13916602830;
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Shanghai YuLue Chemical Co., Ltd.
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021-60345187 13671753212
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Nanjing Derno Pharmaceutical Technology Co., Ltd.
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Wuxi Asia Peptide Biotechnology Limited Company
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Aikon International Limited
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17702-88-4, 2-AMINOCAPRIC ACIDRelated Search:


  • 2-AMINOCAPRIC ACID
  • 2-AMINODECANOIC ACID
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  • 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