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Oxaceprol

Product Name
Oxaceprol
CAS No.
33996-33-7
Chemical Name
Oxaceprol
Synonyms
NAHP;CO-61;AHP-200;Jonctum;Ac-L-Hyp;AC-HYP-OH;OXACEPROL;trans<;N-AC-L-HYP;Ac-L-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)
pka
3.48±0.40(Predicted)
form 
Crystalline Powder
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
$175
Updated
2025/07/31
Usbiological
Product number
260538
Product name
Acetyl-L-4-hydroxyproline
Packaging
50g
Price
$326
Updated
2021/12/16
Biosynth Carbosynth
Product number
FA47431
Product name
Acetyl-L-4-hydroxyproline
Packaging
500g
Price
$400
Updated
2021/12/16
Chem-Impex
Product number
02614
Product name
Acetyl-L-trans-4-hydroxyproline,95%(TLC)
Purity
95%(TLC)
Packaging
25G
Price
$509.6
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
AAA0001569
Product name
N-ACETYL-HYPHYDROXYPROLINE
Purity
95.00%
Packaging
5G
Price
$816
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

reaction suitability

reaction type: solution phase peptide synthesis

Oxaceprol Preparation Products And Raw materials

Raw materials

Preparation Products

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Oxaceprol Suppliers

Tel
18210857532; 18210857532
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
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China
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+49 3493/605464
Fax
+49 3493/605470
Email
sales@intatrade.de
Country
Germany
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400-6106006
Fax
021-67582001/03/05
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saleschina@alfa-asia.com
Country
China
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021-021-58432009 400-005-6266
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021-58436166
Email
sales8178@energy-chemical.com
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China
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13817811078
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86-021-50426522,50426273
Email
sales@jingyan-chemical.com
Country
China
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001-857-928-2050 or 1-888-588-9418
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001-617-206-9595
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sales@chemreagents.com
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United States
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86-021-51714507
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China
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China
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China
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15527768836
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1791901229@qq.com
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China
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View Lastest Price from Oxaceprol manufacturers

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 Chuanghai Biotechnology Co., Ltd
Product
Oxaceprol 33996-33-7
Price
US $10.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2024-11-13
Hebei Zhuanglai Chemical Trading Co Ltd
Product
Oxaceprol 33996-33-7
Price
US $79.00-38.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20ton
Release date
2024-11-21

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
  • <I>trans<
  • NAHP
  • Oxaceprol (N-acetyl-L-hydroxyproline)
  • Oxaceprol, 10 mM in DMSO
  • 33996-33-7
  • 33966-33-7
  • 33996-33-8
  • C7H11NO4
  • Peptide Synthesis
  • Proline Derivatives
  • Specialty Synthesis
  • Unnatural Amino Acid Derivatives