ChemicalBook > CAS DataBase List > Oxaceprol

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
More
Less

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)
More
Less

Safety

Hazard Codes 
Xi
Risk Statements 
41
Safety Statements 
26-36
WGK Germany 
3
10
TSCA 
Yes
HS Code 
29339900
More
Less

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.

More
Less

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
More
Less

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

More
Less

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
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
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
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
15527768850
Email
1791901229@qq.com
Country
China
ProdList
8849
Advantage
52
Shanghai CoachChem Co., Ltd.
Tel
021-67299971
Fax
021-67299972
Email
marketing@coachchem.com
Country
China
ProdList
85
Advantage
62
Nanjing Rate Biochemicals CO., LTD.
Tel
+86-(0)25-84931986,(0)18951962398
Fax
+86-(0)25-84931686
Country
China
ProdList
70
Advantage
62
Chengdu Ai Keda Chemical Technology Co., Ltd.
Tel
4008-755-333 18080918076
Fax
028-86757656
Email
800078821@qq.com
Country
China
ProdList
9725
Advantage
55
Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Fax
010-65763397
Email
waley188@sohu.com
Country
China
ProdList
12338
Advantage
58
Shanghai T&W Pharmaceutical Co., Ltd.
Tel
+86 21 61551611
Fax
+86 21 50676805
Country
China
ProdList
9901
Advantage
58
Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
18521735133 18521732826;
Fax
021-50323701
Email
market@aladdin-e.com
Country
China
ProdList
25015
Advantage
65
Cantotech Chemicals, Ltd.
Tel
86-0755-86635001
Fax
86-0755-22642228
Email
cantotech@126.com
Country
China
ProdList
4576
Advantage
55
Shanghai Yolne Chemical Co., Ltd.
Tel
021-62960152
Fax
021-52212593
Email
934678158@qq.com
Country
China
ProdList
9906
Advantage
55
Nanjing Sunlida Biological Technology Co., Ltd.
Tel
025-57798810
Fax
025-57019371
Email
sales@sunlidabio.com
Country
China
ProdList
3750
Advantage
55
TargetMol Chemicals Inc.
Tel
021-021-33632979 15002134094
Fax
021-33632979
Email
marketing@targetmol.com
Country
China
ProdList
7934
Advantage
58
Bide Pharmatech Ltd.
Tel
400-1647117 15221909166
Fax
+86-21-61629029
Email
product02@bidepharm.com
Country
China
ProdList
41438
Advantage
60
Chengdu Sino-Strong Pharmaceutical Co.,Ltd.
Tel
0086-28-82783659 13688347223
Fax
028-82783880
Email
sales@sino-strong.com.cn
Country
China
ProdList
124
Advantage
60
Chengdu HuaXia Chemical Reagent Co. Ltd
Tel
400-1166-196 13458535857
Fax
QQ:800101999
Email
cdhxsj@163.com
Country
China
ProdList
13358
Advantage
58
Finetech Industry Limited
Tel
027-87465837 19945049750
Fax
027-8777-2287
Email
sales@finetechnology-ind.com
Country
China
ProdList
9636
Advantage
58
Sichuan Ampebiochem Co., Ltd.
Tel
028-65294243
Fax
028-85275169
Email
sales@ampebiochem.com
Country
China
ProdList
1017
Advantage
58
Shanghai YuLue Chemical Co., Ltd.
Tel
021-60345187 13671753212
Fax
021-34702061
Email
lzz841106@aliyun.com
Country
China
ProdList
10287
Advantage
55
Nanjing Derno Pharmaceutical Technology Co., Ltd.
Tel
025-86957866 13952093866
Fax
025-68661287
Email
sales@dernopharm.com
Country
China
ProdList
924
Advantage
58
Hubei Jusheng Technology Co.,Ltd
Tel
027-59599241 18871490274
Fax
027-59599241
Email
1400878000@qq.com
Country
China
ProdList
9972
Advantage
58
Chizhou Kailong Import and Export Trade Co., Ltd.
Tel
Fax
-
Email
xg01_gj@163.com
Country
China
ProdList
9503
Advantage
50
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51471
Advantage
80
Kono Chem Co.,Ltd
Tel
15829389671
Fax
029-86107037
Email
info@konochemical.com
Country
China
ProdList
554
Advantage
55
Shanghai GL Peptide Ltd.
Tel
+86-21-61263310; 13764994101 13764994101
Fax
021-61263399
Email
fisherwang@glschina.com
Country
China
ProdList
8457
Advantage
55
ShangHai Siyan Biological Technology Co., Ltd.
Tel
021-50908862,442785678,326799392 18721037013
Fax
021-50908862
Email
siyansales@126.com
Country
China
ProdList
9638
Advantage
58
Henan CoreyChem Co., Ltd
Tel
0371-86658258
Fax
0371-60996044
Email
info@coreychem.com
Country
China
ProdList
10457
Advantage
58
Shanghai Qiao Chemical Science Co., Ltd
Tel
021-58892003
Email
info@qiaochem.com
Country
China
ProdList
5881
Advantage
65
Shanghai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847; 18021002903
Fax
QQ:3008007432
Email
3008007409@qq.com
Country
China
ProdList
27322
Advantage
60
parabiochem
Tel
025-83453382-8005
Fax
025-83453382
Email
sale@parabiochem.com
Country
China
ProdList
9604
Advantage
55
Lancrix Chemicals
Tel
86-21-50817262
Fax
86-21-57712035
Email
sales@lancrix.com
Country
China
ProdList
1503
Advantage
55
Raw material medicin reagent co.,Ltd
Tel
025-57798860
Email
sales@njromanme.com
Country
China
ProdList
4534
Advantage
58
Grader reagent
Tel
18221735425
Email
sales@xinpingchem.com
Country
China
ProdList
9951
Advantage
58
Shanghai SuperLan Chemcial Technique Centre
Tel
021-2022843681 15618226720
Fax
+86-21-51601218
Email
chaolaichem@foxmail.com
Country
China
ProdList
9058
Advantage
58
Wuxi Asia Peptide Biotechnology Limited Company
Tel
0510-83583050 13771062561
Fax
0510-83583039
Email
willsun@peptide-search.com
Country
China
ProdList
6716
Advantage
58
Beijing Solarbio Science & Tecnology Co., Ltd.
Tel
010-50973130 4009686088
Email
3193328036@qq.com
Country
China
ProdList
29797
Advantage
68
Amadis Chemical Company Limited
Tel
571-89925085
Fax
0086-571-89925065
Email
sales@amadischem.com
Country
China
ProdList
131981
Advantage
58
Wuhan Magic Biological Technology Co., Ltd.
Tel
18872289958、027-52304252、3400508168
Fax
027-52304252
Email
3400508168@qq.com
Country
China
ProdList
1910
Advantage
55
Nanjing Peptide Biotech Ltd.
Tel
025-58361106-805 13082558573
Fax
025-58361106-806
Email
liugang@njpeptide.com
Country
China
ProdList
9961
Advantage
55
Shanghai Kangman Biological Technology Co., Ltd.
Tel
18800375331
Fax
021-50908862
Email
kangmansales@163.com
Country
China
ProdList
7580
Advantage
55
Amatek Scientific Co. Ltd.
Tel
0512-56316828
Fax
0512-56316826
Email
info@amateksci.com
Country
China
ProdList
28821
Advantage
58
JinJin Le Chemical Co., Ltd
Tel
10106090
Email
jjlchem2@163.com
Country
China
ProdList
9986
Advantage
58
Shanghai BaiShun Biological Technology Co., Ltd
Tel
021-37581181
Fax
021-57456066
Email
sales@chem-mall.com
Country
China
ProdList
10335
Advantage
58
Shanghai Yongzhi chemical-Technology Co., Ltd.
Tel
021-60944093 18516153908 13917602471
Fax
021-60944093
Email
mianyanghaodao@aliyun.com
Country
China
ProdList
411
Advantage
58
Shanghai Zhen Li Biological Technology Co., Ltd
Tel
021-16621358918; 18516310516
Fax
13045646768
Email
zhenlipharma888@163.com
Country
China
ProdList
1979
Advantage
58
More
Less

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