ChemicalBook > CAS DataBase List > H-LYS(ALLOC)-OH

H-LYS(ALLOC)-OH

Product Name
H-LYS(ALLOC)-OH
CAS No.
6298-03-9
Chemical Name
H-LYS(ALLOC)-OH
Synonyms
NSC 45852;L-Lys(Aloc)-OH;nδ-alloc-l-lysine;H-LYS(ALLOC)-OH USP/EP/BP;Nε-Allyloxycarbonyl-L-lysine;Ne-Allyloxycarbonyl-L-lysine;H-Lys(Aloc)-OH (E-3065.0001);N6-[(2-Propen-1-yloxy)carbonyl]-L-lysine;L-Lysine, N6-[(2-propen-1-yloxy)carbonyl]-;(S)-6-(((Allyloxy)carbonyl)aMino)-2-aMinohexanoic acid
CBNumber
CB1973060
Molecular Formula
C10H18N2O4
Formula Weight
230.26
MOL File
6298-03-9.mol
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H-LYS(ALLOC)-OH Property

Boiling point:
414.9±45.0 °C(Predicted)
Density 
1.153±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
2.53±0.24(Predicted)
form 
solid
Appearance
White to off-white Solid
optical activity
[α]20/D +18.5±1°, c =1% in 1 M HCl
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Safety

Risk Statements 
43
Safety Statements 
36/37
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H317May cause an allergic skin reaction

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
74218
Product name
H-Lys(Alloc)-OH
Purity
≥99.0%
Packaging
1G
Price
$246
Updated
2025/07/31
Usbiological
Product number
240877
Product name
Ne-Allyloxycarbonyl-L-lysine
Packaging
1g
Price
$266
Updated
2021/12/16
Usbiological
Product number
285695
Product name
Ne-Allyloxycarbonyl-L-lysine
Packaging
500mg
Price
$340
Updated
2021/12/16
TRC
Product number
L488863
Product name
H-Lys(Alloc)-OH
Packaging
50mg
Price
$45
Updated
2021/12/16
TRC
Product number
L488863
Product name
H-Lys(Alloc)-OH
Packaging
100mg
Price
$60
Updated
2021/12/16
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H-LYS(ALLOC)-OH Chemical Properties,Usage,Production

Uses

peptide synthesis

reaction suitability

reaction type: solution phase peptide synthesis

Synthesis

372-75-8

2937-50-0

6298-03-9

Step 5. A mixed solution of L-citrulline (10 g, 68.4 mmol) and basic copper carbonate (15.12 g, 68.4 mmol) in distilled water (100 mL) was heated to reflux for 30 minutes. Solids generated during refluxing were removed by thermal filtration. The filtrate was cooled to 0 °C and the pH was adjusted to 9 by addition of anhydrous sodium carbonate (1.0 g). allyl chloroformate (10.8 mL, 102.6 mmol) was added slowly and dropwise while stirring at 0 °C. During dropwise addition, the pH of the reaction mixture was maintained at 9 by addition of anhydrous sodium carbonate (20 g). the reaction mixture was gradually warmed up to room temperature with continuous stirring for 12 h. The reaction was carried out by filtration. Upon completion of the reaction, the resulting blue solid product was quantitatively collected by filtration. The resulting copper salt solid of Orn (Alloc) was suspended in distilled water (200 mL) and thioacetamide (6.511 g, 86.66 mmol, 2 equiv) was added. The basic suspension was stirred at 50 °C for 3 h, during which time the solid gradually dissolved. Subsequently, the solution was acidified to pH 2 with 2 M hydrochloric acid and boiling was continued for 5 min. The resulting copper sulfide precipitate was removed by filtration. The filtrate was concentrated under reduced pressure to about 100 mL, at which point the hydrochloride product of Orn (Alloc) precipitated quantitatively as a white solid.

References

[1] Patent: WO2015/95227, 2015, A2. Location in patent: Page/Page column 168; 169

H-LYS(ALLOC)-OH Preparation Products And Raw materials

Raw materials

Preparation Products

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H-LYS(ALLOC)-OH Suppliers

Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44801
Advantage
61
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Country
China
ProdList
42934
Advantage
64
Bide Pharmatech Ltd.
Tel
400-164-7117 13681763483
Fax
+86-21-61629029
Email
product02@bidepharm.com
Country
China
ProdList
39966
Advantage
60
Wuxi Zhongkun Biochemical Technology Co., Ltd.
Tel
0510-85629785 18013409632
Fax
051085625359
Email
sales@reading-chemicals.com
Country
China
ProdList
15178
Advantage
58
Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.
Tel
025-66028182 18626450290
Email
yftan@aikonchem.com
Country
China
ProdList
16679
Advantage
50
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51395
Advantage
80
Chengdu Chuangkecheng Biological Technology Co., Ltd.
Tel
028-028-0000000 13008177686
Fax
15928581901
Email
sales@ckcbiotech.com
Country
China
ProdList
904
Advantage
55
Shanghai GL Peptide Ltd.
Tel
+86-21-61263340; 17609490614 13764994101
Fax
021-61263399
Email
fisherwang@glschina.com
Country
China
ProdList
8258
Advantage
55
Wuxi Asia Peptide Biotechnology Limited Company
Tel
0510-83583050 13771062561
Fax
0510-83583039
Email
willsun@peptide-search.com
Country
China
ProdList
6716
Advantage
58
Shanghai Haohong Pharmaceutical Co., Ltd.
Tel
400-8210725 400821072
Fax
021-58955996
Email
malulu@leyan.com
Country
China
ProdList
25000
Advantage
58
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View Lastest Price from H-LYS(ALLOC)-OH manufacturers

Career Henan Chemical Co
Product
H-LYS(ALLOC)-OH 6298-03-9
Price
US $1.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
1kg,5kg,100kg
Release date
2019-07-04

6298-03-9, H-LYS(ALLOC)-OHRelated Search:


  • nδ-alloc-l-lysine
  • (S)-6-(((Allyloxy)carbonyl)aMino)-2-aMinohexanoic acid
  • NSC 45852
  • (2S)-2-Amino-6-[[(prop-2-en-1-yloxy)carbonyl]amino]hexanoic acid
  • N6-[(2-Propen-1-yloxy)carbonyl]-L-lysine
  • L-Lys(Aloc)-OH
  • Ne-Allyloxycarbonyl-L-lysine
  • (2S)-2-amino-6-(prop-2-enoxycarbonylamino)hexanoic acid
  • L-Lysine, N6-[(2-propen-1-yloxy)carbonyl]-
  • H-LYS(ALLOC)-OH USP/EP/BP
  • Nε-Allyloxycarbonyl-L-lysine
  • H-Lys(Aloc)-OH (E-3065.0001)
  • 6298-03-9
  • SiChem