ChemicalBook--->CAS DataBase List--->37159-97-0

37159-97-0

37159-97-0 Structure

37159-97-0 Structure
IdentificationBack Directory
[Name]

L-PROLINE-(4-3H(N))
[CAS]

37159-97-0
[Synonyms]

CL061
L-PROLINE-(4-3H(N))
L-PROLINE-(4-3H(N)) USP/EP/BP
[Molecular Formula]

C5H9N1O2
[MDL Number]

MFCD00135800
[MOL File]

37159-97-0.mol
[Molecular Weight]

115.13
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[form ]

aqueous ethanol solution
Safety DataBack Directory
[Hazard Codes ]

R
[RIDADR ]

UN 2910 7
[WGK Germany ]

3
Questions And AnswerBack Directory
[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.
Hazard InformationBack Directory
[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.
37159-97-0 suppliers list
Company Name: ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
Tel: +86-13017695106 +86-13676922317 , +86-13676922317
Website:
Company Name: Henan Tianfu Chemical Co.,Ltd.
Tel: +86-0371-55170693 +86-19937530512 , +86-19937530512
Website: https://www.tianfuchem.com/
Company Name: Hubei Jusheng Technology Co.,Ltd.
Tel: 18871490254
Website: www.hubeijusheng.com
Company Name: career henan chemical co
Tel: +86-0371-86658258 +8613203830695 , +8613203830695
Website: www.coreychem.com
Company Name: Hubei Ipure Biology Co., Ltd
Tel: +8613367258412 , +8613367258412
Website: http://www.ipurechemical.com
Company Name: Shaanxi Dideu Medichem Co. Ltd
Tel: +86-029-89586680 +86-18192503167 , +86-18192503167
Website: www.dideu.com
Company Name: Zhuoer Chemical Co., Ltd
Tel: 02120970332; +8613524231522 , +8613524231522
Website: http://www.zhuoerchem.com/
Company Name: Guangdong Zhaoqing Xinghu Biotechnology Co., Ltd. Xinghu Biochemical Pharmaceutical Factory  Gold
Tel: 0758-2292360
Website: www.starlake.com.cn
Company Name: Shanghai T&W Pharmaceutical Co., Ltd.  
Tel: +86 21 61551611
Website: www.trustwe.com
Company Name: Shanghai QianYan Bio-technology Co., Ltd  
Tel: 02781293128
Website: www.chemicalbook.com/ShowSupplierProductsList19348/0_EN.htm
Company Name: Grader reagent  
Tel: 18221735425
Website: www.shxinping.net
Company Name: Wuhan FengyaoTonghui Chemical Products Co., Ltd.  
Tel: 027-87466105 15377573527
Website: www.chemicalbook.com/ShowSupplierProductsList30440/0_EN.htm
Company Name: Nanjing crow LuNing pharmaceutical technology co., LTD  
Tel: 13382066392
Website: www.chemicalbook.com/ShowSupplierProductsList30681/0_EN.htm
Company Name: Wuhan plov Biotechnology Co., Ltd  
Tel: 17612776928
Website: puluofu.company.lookchem.cn/
Company Name: Hubei Wanye Zhongcheng Chemical Reagent Co., Ltd.  
Tel: 18671296875
Website: https://www.wanyezhongcheng.com
Company Name: Wuhamplov Biotechnology Co., LTD  
Tel: 00-18372743325 18372743325
Website: www.puluofubio.com/
Company Name: Minglong (Xianning) Pharmaceutical Co., LTD  
Tel: 186-7296-9259 18771307593
Website: www.minglongchemistry.com/shop/
Company Name: Wuhan Yuancheng Gongchuang Technology Co., Ltd.  
Tel: 17683743113
Website: www.chemicalbook.com/ShowSupplierProductsList1361174/0_EN.htm
Tags:37159-97-0 Related Product Information
70-26-8 7004-03-7 56-40-6

  • HomePage | Member Companies | Advertising | Contact us | Previous WebSite | MSDS | CAS Index | CAS DataBase | Privacy | Terms | About Us
  • All products displayed on this website are only for non-medical purposes such as industrial applications or scientific research, and cannot be used for clinical diagnosis or treatment of humans or animals. They are not medicinal or edible.
    According to relevant laws and regulations and the regulations of this website, units or individuals who purchase hazardous materials should obtain valid qualifications and qualification conditions.
  • Copyright © 2023 ChemicalBook All rights reserved.