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L-PROLINE-(4-3H(N))

Application
Product Name
L-PROLINE-(4-3H(N))
CAS No.
37159-97-0
Chemical Name
L-PROLINE-(4-3H(N))
Synonyms
CL061;L-PROLINE-(4-3H(N));L-PROLINE-(4-3H(N)) USP/EP/BP
CBNumber
CB8500061
Molecular Formula
C5H9NO2
Formula Weight
115.13046
MOL File
37159-97-0.mol
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L-PROLINE-(4-3H(N)) Property

storage temp. 
2-8°C
form 
aqueous ethanol solution
InChI
InChI=1/C5H9NO2/c7-5(8)4-2-1-3-6-4/h4,6H,1-3H2,(H,7,8)/t4-/s3
InChIKey
ONIBWKKTOPOVIA-UFLUHPNLNA-N
SMILES
N1CCC[C@H]1C(O)=O |&1:4,r|
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Safety

Hazard Codes 
R
RIDADR 
UN 2910 7
WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

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L-PROLINE-(4-3H(N)) Chemical Properties,Usage,Production

Application

1. Pharmaceutical Applications: Amino acid drugs. One of the raw materials for compound amino acid large-volume parenteral solutions. Used for malnutrition, protein deficiency, severe gastrointestinal diseases, and protein supplementation after burns and surgery. No obvious toxic side effects. 2. Improving Plant Cold Resistance: Proline (Pro) is a component of plant proteins and can exist widely in a free state in plants. Under stress conditions such as drought and salinity, many plants accumulate large amounts of proline. Besides acting as an osmotic regulator in plant cytoplasm, accumulated proline plays an important role in stabilizing the structure of biological macromolecules, reducing cell acidity, detoxifying ammonia, and regulating cellular redox potential as an energy reservoir. Under adverse conditions (drought, salinity, heat, cold, freezing), the proline content in plants increases significantly. The proline content in plants reflects their stress resistance to a certain extent; drought-resistant varieties often accumulate more proline. Therefore, measuring proline content can be used as a physiological indicator for drought-resistant breeding. In addition, due to its strong hydrophilicity, proline can stabilize protoplasmic colloids and metabolic processes within tissues, thus lowering the freezing point and preventing cell dehydration. Under low-temperature conditions, increased proline in plant tissues can improve cold resistance, and therefore can also be used as a physiological indicator for cold-resistant breeding.
3. In Vivo Functions
In vivo, proline is not only an ideal osmotic regulator, but also a protective substance for membranes and enzymes, as well as a free radical scavenger, thus protecting plant growth under osmotic stress. Proline also plays a role in regulating cytoplasmic osmotic balance regarding the accumulation of potassium ions, another important osmotic regulator in vacuoles.
4. Industrial Applications
In the synthetic industry, proline can participate in inducing asymmetric reactions and can be used as a catalyst for hydrogenation, polymerization, and aqueous reactions. When used as a catalyst for these reactions, it exhibits high activity and good stereospecificity.
5. Other Applications
5.1 Proline and its derivatives are commonly used as symmetrical catalysts in organic reactions; the reduction of CBS and the catalytic aldol condensation reaction of proline are prominent examples.
5.2 During brewing, proteins rich in proline bound to polyphenols can produce haze (turbidity).
5.3 Raw material for the synthesis of cholesterol ester inhibitors.
5.4 Flavoring agent; when heated with sugar, it undergoes an amino-hydroxyl reaction to generate substances with special aromas.

Definition

ChEBI: L-proline is pyrrolidine in which the pro-S hydrogen at position 2 is substituted by a carboxylic acid group. L-Proline is the only one of the twenty DNA-encoded amino acids which has a secondary amino group alpha to the carboxyl group. It is an essential component of collagen and is important for proper functioning of joints and tendons. It also helps maintain and strengthen heart muscles. It has a role as a micronutrient, a nutraceutical, an algal metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite, a mouse metabolite and a member of compatible osmolytes. It is a glutamine family amino acid, a proteinogenic amino acid, a proline and a L-alpha-amino acid. It is a conjugate base of a L-prolinium. It is a conjugate acid of a L-prolinate. It is an enantiomer of a D-proline. It is a tautomer of a L-proline zwitterion.

L-PROLINE-(4-3H(N)) Preparation Products And Raw materials

Raw materials

Preparation Products

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L-PROLINE-(4-3H(N)) Suppliers

Guangdong Zhaoqing Xinghu Biotechnology Co., Ltd. Xinghu Biochemical Pharmaceutical Factory
Tel
0758-2292360
Fax
0758-2292621
Country
China
ProdList
4
Advantage
58
Shanghai T&W Pharmaceutical Co., Ltd.
Tel
+86 21 61551611
Fax
+86 21 50676805
Country
China
ProdList
9891
Advantage
58
Shanghai QianYan Bio-technology Co., Ltd
Tel
02781293128
Email
orders@biochemsafebuy.com
Country
China
ProdList
9923
Advantage
55
Grader reagent
Tel
18221735425
Email
sales@xinpingchem.com
Country
China
ProdList
9942
Advantage
58
Wuhan FengyaoTonghui Chemical Products Co., Ltd.
Tel
027-87466105 15377573527
Email
2678564200@qq.com
Country
China
ProdList
17987
Advantage
58
Nanjing crow LuNing pharmaceutical technology co., LTD
Tel
13382066392
Country
CHINA
ProdList
4877
Advantage
58
Hubei Ipure Biology Co., Ltd
Tel
+8613367258412
Fax
18062427325
Email
ada@ipurechemical.com
Country
China
ProdList
10237
Advantage
58
Zhuoer Chemical Co., Ltd
Tel
02120970332; +8613524231522
Fax
+86-21-58816016
Email
sales@zhuoerchem.com
Country
China
ProdList
2904
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58
Shaanxi Dideu Medichem Co. Ltd
Tel
+86-029-89586680 +86-18192503167
Fax
+86-29-88380327
Email
1026@dideu.com
Country
China
ProdList
8025
Advantage
58
Hubei Jusheng Technology Co.,Ltd.
Tel
18871490254
Fax
027-59599243
Email
linda@hubeijusheng.com
Country
CHINA
ProdList
28172
Advantage
58
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View Lastest Price from L-PROLINE-(4-3H(N)) manufacturers

ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
Product
L-(-)-Proline 37159-97-0
Price
US $2.00-5.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
100kg
Release date
2025-07-08
Career Henan Chemical Co
Product
L-PROLINE-(4-3H(N)) 37159-97-0
Price
US $1.00/KG
Min. Order
1KG
Purity
99
Supply Ability
100kg
Release date
2019-12-18

37159-97-0, L-PROLINE-(4-3H(N))Related Search:


  • L-PROLINE-(4-3H(N))
  • CL061
  • L-PROLINE-(4-3H(N)) USP/EP/BP
  • 37159-97-0