| Identification | More | [Name]
2-Pyrrolidinecarboxylic acid | [CAS]
147-85-3 | [Synonyms]
2-pyrrolidinecarboxylic acid
FEMA 3319
H-L-PRO-OH
H-PRO-OH
H-PYRD(2)-OH
L-2-PYRROLIDINECARBOXYLIC ACID
L-PRO
L(-)-PROLINE
L-PROLINE
L-PYRROLIDINE-2-CARBOXYLIC ACID
PRO
PROLINE
PROLINE, L-
(S)-(-)-PROLINE
(S)-(-)-PYRROLIDINE-2-CARBOXYLIC ACID
(S)-PYRROLIDINE-2-CARBOXYLIC ACID
(2S)-Pyrrolidin-2-carbonsαure
(s)-2-pyrrolidinecarboxylicaci
(s)-2-pyrrolidinecarboxylicacid
(S)-Prolin | [EINECS(EC#)]
205-702-2 | [Molecular Formula]
C5H9NO2 | [MDL Number]
MFCD00064318 | [Molecular Weight]
115.13 | [MOL File]
147-85-3.mol |
| Chemical Properties | Back Directory | [Appearance]
White crystalline powder | [Melting point ]
228 °C (dec.) (lit.) | [alpha ]
-85.5 º (c=4, H2O) | [Boiling point ]
215.41°C (rough estimate) | [bulk density]
500kg/m3 | [density ]
1.35
| [vapor pressure ]
0Pa at 25℃ | [FEMA ]
3319 | [refractive index ]
-85 ° (C=4, H2O) | [storage temp. ]
Store at RT. | [solubility ]
H2O: 50 mg/mL
| [form ]
powder
| [pka]
1.95, 10.64(at 25℃) | [color ]
White | [Odor]
at 100.00 %. odorless | [PH]
6.0-7.0 (25℃, 1M in H2O) | [Stability:]
Stable. Incompatible with strong oxidizing agents. | [biological source]
synthetic | [Odor Type]
odorless | [Optical Rotation]
[α]20/D 85.0±1.0°, c = 5% in H2O | [Water Solubility ]
soluble | [Sensitive ]
Hygroscopic | [λmax]
λ: 260 nm Amax: 0.05
λ: 280 nm Amax: 0.05 | [JECFA Number]
1425 | [Merck ]
14,7780 | [BRN ]
80810 | [Cosmetics Ingredients Functions]
SKIN CONDITIONING
HAIR CONDITIONING | [InChI]
1S/C5H9NO2/c7-5(8)4-2-1-3-6-4/h4,6H,1-3H2,(H,7,8)/t4-/m0/s1 | [InChIKey]
ONIBWKKTOPOVIA-UHFFFAOYSA-N | [SMILES]
OC(=O)[C@@H]1CCCN1 | [LogP]
-2.54 at 20℃ | [CAS DataBase Reference]
147-85-3(CAS DataBase Reference) | [NIST Chemistry Reference]
Proline(147-85-3) | [EPA Substance Registry System]
147-85-3(EPA Substance) |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H315-H319-H335 | [Precautionary statements ]
P261-P271-P280 | [Hazard Codes ]
Xi,Xn | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin .
R22:Harmful if swallowed. | [Safety Statements ]
S24/25:Avoid contact with skin and eyes .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [RTECS ]
TW3584000
| [F ]
3-10 | [TSCA ]
Yes | [REACH Registrations]
Active | [HS Code ]
29339990 | [Storage Class]
13 - Non Combustible Solids | [Hazardous Substances Data]
147-85-3(Hazardous Substances Data) | [Toxicity]
LD50 orally in Rabbit: > 5110 mg/kg |
| Hazard Information | Back Directory | [Chemical Properties]
L-Proline(147-85-3), an amino acid, is odorless or has a slight, characteristic odor with a slightly sweet taste.
| [Occurrence]
Reported found as a component in many proteins; also widely occurring as the free acid in natural products. A
major constituent of collagen, the main fibrous protein found in bone, cartilage and other connective tissue. | [Uses]
L-Proline(147-85-3) is an amino acid and precursor (with vitamin C) for collagen, the building block of the structure of tendons, ligaments, arteries, veins and muscles. It is important in wound healing.
| [Definition]
ChEBI: L-proline (147-85-3) 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.
| [Preparation]
From α-piperidone; from cyclopentantone; from l-glutamic acid. | [Biotechnological Production]
Direct fermentation using analogue-resistant mutants of coryneform bacteria or Serratia marcescens is an economic production method. An isoleucine auxotrophic mutant of Brevibacterium flavum having resistance to sulfaguanidine and D,L-3,4-dehydroproline (DP) is able to accumulate 40 g/L L-proline. Brevibacterium flavum AP113 is claimed to produce 97.5 g/L L-proline; this mutant is characterized by isoleucine auxotrophy, resistance to DP, and osmotic pressure and incapable to degrade Lproline. A proline oxidase-less strain of Serratia marcescens, having resistance to DP, thiazoline-4-carboxylate and azetidine-2-carboxylate, overproduces 58.5 g/L L-proline into the culture medium. By amplification of the genes proA and proB in this type of regulatory mutant, a construct was obtained which yields 75 g/L L-proline.
| [benefits]
L-proline(147-85-3) is considered a non-essential amino acid as it can be synthesised from arginine via the urea cycle in liver, and from glutamine/glutamic acid in the intestinal epithelium. It has a number of beneficial properties including connective tissue strengthening, Stronger Connective Tissue, Decreased Risk Of Heart Disease, Maintenance Of Muscle Tissueand skin health.
| [General Description]
L-Proline(147-85-3) is a non-essential amino acid. Peptides bond to proline, making it a useful building block for proteins. It can be used as a cell culture media component for the commercial biomanufacturing of therapeutic recombinant proteins and monoclonal antibodies. | [Flammability and Explosibility]
Nonflammable | [Biochem/physiol Actions]
Proline is a cyclic, non-essential, hydrophobic amino acid. It is a proteinogenic amino acid which is crucial for primary metabolism. In peptide chains, proline residues confer structural constraints and enhance the susceptibility of proximal peptide bonds to protease activity. | [Side effects]
The only known side effects are reactions from taking too much L-proline, like all amino acids. It causes toxicity levels and amino acid imbalances in your body. | [Purification Methods]
A likely impurity is hydroxyproline. Purify L-proline via its picrate which is crystallised twice from water, then decomposed with 40% H2SO4. The picric acid is extracted with diethyl ether, the H2SO4 in solution is precipitated with Ba(OH)2, and the filtrate is evaporated. The residue is crystallised from hot absolute EtOH [Mellan & Hoover J Am Chem Soc 73 3879 1951] or EtOH/Et2O. Its solubility in H2O is >100%. It sublimes at 182-187o/0.3mm with 99.4% recovery and unracemised [Gross & Gradsky J Am Chem Soc 77 1678 1955]. It is hygroscopic and is stored in a desiccator. [Greenstein & Winitz The Chemistry of the Amino Acids J. Wiley, Vol 3 pp 2178-2199 1961, Beilstein 22 III/IV 8, 22/1 V 31.] | [Structure and conformation]
L-proline(147-85-3), also known as L-pyrrolidine-2-carboxylic acid, is a neutral amino acid. Although proline is classified as an amino acid, it is strictly speaking an imino acid, since it contains an imino group (carbon-nitrogen double bond). Due to its cyclic pyrrolidine side chain it is classified as a nonpolar aliphatic amino acid.
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J & K SCIENTIFIC LTD.
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18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
Alfa Aesar
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400-6106006 |
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http://chemicals.thermofisher.cn |
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