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Oxaceprol

Product Name
Oxaceprol
CAS No.
33996-33-7
Chemical Name
Oxaceprol
Synonyms
CO-61;AHP-200;Jonctum;Ac-L-Hyp;AC-HYP-OH;OXACEPROL;N-AC-L-HYP;Ac-L-Hyp-OH;trans-l-prolin;Hyp4001Ac-Hyp-Oh
CBNumber
CB2482503
Molecular Formula
C7H11NO4
Formula Weight
173.17
MOL File
33996-33-7.mol
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Oxaceprol Property

Melting point:
132-133 °C (dec.)(lit.)
alpha 
-119 º (c=4 in H2O)
Boiling point:
303.8°C (rough estimate)
Density 
1.3346 (rough estimate)
vapor pressure 
0Pa at 20℃
refractive index 
1.4490 (estimate)
storage temp. 
Sealed in dry,2-8°C
solubility 
DMSO : ≥ 32 mg/mL (184.79 mM)
form 
Crystalline Powder
pka
3.48±0.40(Predicted)
color 
White
optical activity
[α]20/D 119°, c = 4 in H2O
Merck 
14,6903
BRN 
84043
InChIKey
BAPRUDZDYCKSOQ-RITPCOANSA-N
LogP
-1.51 at 20℃
CAS DataBase Reference
33996-33-7(CAS DataBase Reference)
EPA Substance Registry System
L-Proline, 1-acetyl-4-hydroxy-, (4R)- (33996-33-7)
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Safety

Hazard Codes 
Xi
Risk Statements 
41
Safety Statements 
26-36
WGK Germany 
3
10
TSCA 
Yes
HS Code 
29339900
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H318Causes serious eye damage

Precautionary statements

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

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

Sigma-Aldrich
Product number
441562
Product name
trans-1-Acetyl-4-hydroxy-L-proline
Purity
≥98%
Packaging
10g
Price
$170
Updated
2024/03/01
Alfa Aesar
Product number
B23767
Product name
N-Acetyl-trans-4-hydroxy-L-proline, 99%
Packaging
2g
Price
$40.65
Updated
2024/03/01
Alfa Aesar
Product number
B23767
Product name
N-Acetyl-trans-4-hydroxy-L-proline, 99%
Packaging
10g
Price
$136
Updated
2023/06/20
Alfa Aesar
Product number
B23767
Product name
N-Acetyl-trans-4-hydroxy-L-proline
Purity
99%
Packaging
5g
Price
$79.2
Updated
2023/06/20
Alfa Aesar
Product number
B23767
Product name
N-Acetyl-trans-4-hydroxy-L-proline, 99%
Packaging
50g
Price
$428
Updated
2021/12/16
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Oxaceprol Chemical Properties,Usage,Production

Chemical Properties

White powder

Originator

Jonctum,Merrell,France,1970

Uses

trans-1-Acetyl-4-hydroxy-L-proline can be used:

  • In the stereospecific synthesis of 4-fluoroglutamic acid.
  • To synthesize molecular targets for von Hippel-Lindau (VHL) E3 ubiquitin ligase.
  • As a precursor to synthesize pseudopoly(amino acids) such as poly(trans-4-hydroxy-4-acyl-L-proline ester) and a biodegradable polymer, poly(lactic acid-glycolic acid-4-hydroxyproline).

Manufacturing Process

16.7 g (0.127 mol) of L-hydroxyproline are dissolved in 400 ml of pure boiling acetic acid. With vigorous boiling and agitation, a mixture of 13.7 ml (0.154 mol) of rectified acetic anhydride and 250 ml of pure acetic acid is added during 25 minutes. Without discontinuing the stirring, contents of the flask are cooled by simply causing fresh air to circulate externally round the flask until the temperature of the mixture is reduced to about 35°C. The acetic acid is removed by using a rotary evaporator without exceeding 35°C under a vacuum of about 15 mm Hg. After one hour, 20 ml of anhydrous toluene are added, then 10 ml of anhydrous acetone; the mixture is homogenized and concentrated again as above during 30 minutes. Then 25 ml of acetone are added again, and subsequently 20 ml of toluene, the product being concentrated again; gradually the solution is converted into an amber-colored crystallized paste. Finally, 30 ml of acetone are added to the residue, and stirring is carried out until the oily fraction surrounding the crystals is dissolved. The product is then cooled in an ice chamber, centrifuged, washed with anhydrous acetone and eventually dried, After recrystallization from acetone, crystals are obtained, melting point 132°C.

Therapeutic Function

Antirheumatic

Flammability and Explosibility

Not classified

Oxaceprol Preparation Products And Raw materials

Raw materials

Preparation Products

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Oxaceprol Suppliers

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
INTATRADE GmbH
Tel
+49 3493/605464
Fax
+49 3493/605470
Email
sales@intatrade.de
Country
Germany
ProdList
3576
Advantage
66
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30132
Advantage
84
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44751
Advantage
61
JinYan Chemicals(ShangHai) Co.,Ltd.
Tel
13817811078
Fax
86-021-50426522,50426273
Email
sales@jingyan-chemical.com
Country
China
ProdList
9984
Advantage
60
Pure Chemistry Scientific Inc.
Tel
001-857-928-2050 or 1-888-588-9418
Fax
001-617-206-9595
Email
sales@chemreagents.com
Country
United States
ProdList
10194
Advantage
62
Shanghai Qiude Biochemical Engineering Co., Ltd
Tel
021-37285021 13472570865;
Fax
86-021-51714507
Email
info@pure-chiral.com
Country
China
ProdList
288
Advantage
64
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696;
Email
info@hanhongsci.com
Country
China
ProdList
42982
Advantage
64
Chemsky (shanghai) International Co.,Ltd
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
15421
Advantage
60
XiaoGan ShenYuan ChemPharm co,ltd
Tel
0712-0712-2580635 15527768850
Email
1791901229@qq.com
Country
China
ProdList
8849
Advantage
52
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View Lastest Price from Oxaceprol manufacturers

Shaanxi Haibo Biotechnology Co., Ltd
Product
Oxaceprol 33996-33-7
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10000 Mt/Year
Release date
2023-08-31
WUHAN FORTUNA CHEMICAL CO., LTD
Product
N-Acetyl-L-hydroxyproline 33996-33-7
Price
US $0.00/Kg/Drum
Min. Order
1KG
Purity
98%min
Supply Ability
500kgs
Release date
2021-09-26
Hebei Mojin Biotechnology Co., Ltd
Product
Oxaceprol 33996-33-7
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
50000KG/month
Release date
2023-09-06

33996-33-7, OxaceprolRelated Search:


  • TRANS-1-ACETYL-4-HYDROXY-L-PROLINE
  • N-ACETYLHYDROXY-L-PROLINE
  • N-ACETYL-L-HYDROXYPROLINE
  • N-ALPHA-ACETYL-TRANS-4-HYROXY-L-PYROLLIDINE
  • N-ALPHA-ACETYL-L-4-TRANS-HYDROXYPROLINE
  • N-ALPHA-ACETYL-L-HYROXYPROLINE
  • (-)-1-Acetyl-4β-hydroxy-L-proline
  • (4R)-1-Acetyl-4-hydroxy-L-proline
  • trans-1-Acetyl-4-hydroxy-L-proline 99%
  • trans-1-Acetyl-4-hydroxy-L-proline, >=98%
  • Ac-Hyp-OH≥ 95% (TLC)
  • Nα-Acetyl-L-4-trans-hydroxyproline
  • <I>trans</I>-1-Acetyl-4-hydroxy-<SC>L</SC>-proline
  • Ac-L-Hyp
  • (4R,2S)-1-ACETYL-4-HYDROXY-PYRROLIDINE-2-CARBOXYLIC ACID
  • ACETYL-L-4-HYDROXYPROLINE
  • ACETYL-4-HYDROXY-L-PROLINE
  • AC-HYDROXYPROLINE
  • AC-HYP-OH
  • (2S,4R)-4-HYDROXYPYRROLIDINE-2-CARBOXYLIC ACID
  • OXACEPROL
  • N-ACETYL-4-HYDROXY-L-PROLINE
  • N-AC-L-HYP
  • trans-l-prolin
  • (R)-N-Acetyl-4-hydroxy-L-proline
  • N-Acetyl-4-hydroxyproline
  • N-Acetylhydroxyproline
  • N-Acetyl-trans-4-hydroxy-L-proline
  • AHP-200
  • CO-61
  • Jonctum
  • N-Acetyl-L-hydroxyproline;trans-1-Acetyl-4-hydroxy-L-proline;1-Acetyl-4-hydroxy-2-pyrrolidinecarboxylic acid;AHP-200;CO-61;Jonctum;Oxaceprol
  • 1-Acetyl-4-hydroxy-2-pyrrolidinecarboxylic acid
  • Oxaceprol (trans-1-Acetyl-4-hydroxy-L-proline,monhydrate)
  • Acetyl-trans-4-hydroxy-L-proline
  • Hyp4001Ac-Hyp-Oh
  • L-Proline, 1-acetyl-4-hydroxy-, (4R)- (9CI)
  • (2S,4R)-N-ACETYL-4-HYDROXY-L-PROLINE
  • N-Acetyl-L- 4-Hydroxyproline
  • (2S,4R)-1-Acetyl-4-hydroxypyrrolidine-2-carboxylic acid
  • Ac-L-Hyp-OH
  • N-alpha-Acetyl-L-4-hydroxyproline
  • N-Acetyl-L-Hydroproline
  • L-Proline, 1-acetyl-4-hydroxy-, (4R)-
  • Oxaceprol USP/EP/BP
  • OxaceprolQ: What is Oxaceprol Q: What is the CAS Number of Oxaceprol Q: What is the storage condition of Oxaceprol Q: What are the applications of Oxaceprol
  • 33996-33-7
  • 33966-33-7
  • 33996-33-8
  • C7H11NO4
  • Peptide Synthesis
  • Proline Derivatives
  • Specialty Synthesis
  • Unnatural Amino Acid Derivatives
  • Hydroxyproline [Hyp]
  • PYRROLE
  • API intermediates
  • Amino Acids