L-Serine CAS 56-45-1 (H-Ser-OH) Assay 98.5~101.0% Factory High Quality

Short Description:

Chemical Name: L-Serine 

Synonyms: H-Ser-OH; L-Ser; Abbreviated Ser or S

CAS: 56-45-1 

Assay: 98.5~101.0% (Titration on Dried Basis) 

White Crystals or Crystalline Powder; Slightly Sweet Taste 

Amino Acids, Capacity 500 Tons/Year, High Quality

Contact: Dr. Alvin Huang

Mobile/Wechat/WhatsApp: +86-15026746401

E-Mail: alvin@ruifuchem.com


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Description:

Shanghai Ruifu Chemical Co., Ltd. is the leading supplier of L-Serine (H-Ser-OH; Abbreviated Ser or S) (CAS: 56-45-1) with high quality. As one of the largest amino acids suppliers in China, Ruifu Chemical supplys amino acids meet AJI, USP, EP, JP and FCC standards. We can provide COA, worldwide delivery, small and bulk quantities available. If you are interested in L-Serine, Please contact: alvin@ruifuchem.com

Chemical Properties:

Chemical Name L-Serine 
Synonyms H-Ser-OH; L-Ser; Abbreviated Ser or S; (-)-Serine; Serine; Laevo-Serine; (S)-Serine; L-2-Amino-3-Hydroxypropionic Acid; (S)-2-Amino-3-Hydroxypropionic Acid; (S)-α-Amino-β-Hydroxypropionic Acid; L-3-Hydroxy-2-Aminopropionic Acid; 3-Hydroxy-L-Alanine; β-Hydroxy-L-Alanine
Stock Status In Stock, Production Capacity 500 Tons per Year 
CAS Number 56-45-1  
Molecular Formula C3H7NO3
Molecular Weight 105.09  
Melting Point 222℃(dec.) (lit.)
Density 1.6 
Water Solubility  Soluble in Water, Almost Transparency
Solubility  Freely Soluble in Formic Acid. Practically Insoluble in Ethanol and in Ether. Dissolves in Dilute Hydrochloric Acid
Storage Temp.  Sealed in Dry, Store at Room Temperature
COA & MSDS Available
Classification Amino Acids & Derivatives
Brand Ruifu Chemical

Specifications:

Items Inspection Standards Results
Appearance White Crystals or Crystalline Powder Conforms          
Identification Infrared Absorption Spectrum Conforms
Specific Rotation [α]20/D +14.4° to +15.5° (C=10, 2N HCl)
-33.8°
State of Solution (Transmittance) Clear and Colorless ≥98.0% 98.6%
Chloride (Cl) ≤0.020% <0.020%
Sulfate (SO4) ≤0.020% <0.020%
Ammonium (NH4) ≤0.020% <0.020%
Iron (Fe) ≤10ppm <10ppm
Heavy Metals (Pb) ≤10ppm <10ppm 
Arsenic (As2O3) ≤1.0ppm <1.0ppm
Other Amino Acids Chromatographically Not Detectable  Conforms
Loss on Drying ≤0.20% (at 105℃, 3 hours) 0.15%
Residue on Ignition (Sulfated) ≤0.10% 0.06%
Assay 98.5 to 101.0% (Titration: Dried Basis)     99.7%
pH Test  5.2 to 6.2 (1.0g in 10ml of H2O) 5.5
Organic Volatile Impurities Meets the Requirements Conforms
Origin Non-Animal Source Conforms
Residual Solvents Conforms Conforms
Conclusion Meets AJI97, EP, USP, JP Testing Specifications 
Shelf Life 24 Months From Manufacture Date if Stored Properly
Main Uses Food Additives; Pharmaceuticals; Nutritional Supplement; etc.

Package & Storage:

Package: Fluorinated Bottle, 25kg/bag, 25kg/Cardboard Drum, or according to customer's requirement.

Storage Condition: Store in sealed containers at cool, dry and ventilated warehouse away from incompatible substances. Protect from light and moisture.  

JP16 and USP39 Test Methods:

JP16
L-Serine, when dried, contains not less than 98.5% and not more than 101.0% of C3H7NO3.
Description L-Serine occurs as white crystals or a crystalline powder. It has a slight sweet taste. It is freely soluble in water and in formic acid, and practically insoluble in ethanol (99.5). It dissolves in 2 mol/L hydrochloric acid TS.
Identification Determine the infrared absorption spectrum of L-Serine as directed in the potassium bromide disk method under Infrared Spectrophotometry<2.25>, and compare the spectrum with the Reference Spectrum: both spectra exhibit similar intensities of absorption at the same wave numbers.
Optical rotation <2.49> [a]20D: +14.0°~+16.0°(After dry-ing, 2.5 g, 2 mol/L hydrochloric acid TS, 25 mL, 100 mm).
pH <2.54> The pH of a solution prepared by dissolving 1.0 g of L-Serine in 10 mL of water is between 5.2 and 6.2.
Purity (1) Clarity and color of solution-Dissolve 1.0 g of L-Serine in 10 mL of water: the solution is clear and colorless.
(2) Chloride <1.03>-Perform the test with 0.5 g of L-Serine. Prepare the control solution with 0.30 mL of 0.01mol/L hydrochloric acid VS (not more than 0.021%)
(3) Sulfate <1.14> Perform the test with 0.6 g of L-Serine. Prepare the control solution with 0.35 mL of 0.005mol/L sulfuric acid VS (not more than 0.028%).
(4) Ammonium <1.02>-Perform the test with 0.25 g of L-Serine. Prepare the control solution with 5.0 mL of Standard Ammonium Solution (not more than 0.02%).
(5) Heavy Metals <1.07> Proceed with 2.0 g of L-Serine according to Method 1, and perform the test. Prepare the control solution with 2.0 mL of Standard Lead Solution (not more than 10 ppm).
(6) Iron <1.10> Prepare the test solution with 1.0 g of L-Serine according to Method 1, and perform the test according to Method A. Prepare the control solution with 1.0mL of Standard Iron Solution (not more than 10 ppm).
(7) Related Substances-Dissolve 0.10 g of L-Serine in 10mL of water, and use this solution as the sample solution. Pipet 1 mL of the sample solution, add water to make exactly 10 mL. Pipet 1 mL of this solution, add water to makeexactly 50 mL, and use this solution as the standard solution.Perform the test with these solutions as directed under Thin-layer Chromatography<2.03>. Spot 5mLeachofthesamplesolution and standard solution on a plate of silica gel forthin-layer chromatography. Then develop with a mixture of1-butanol, water and acetic acid (100) (3:1:1) to a distance ofabout 10 cm, and dry the plate at 809C for 30 minutes. Sprayevenly a solution of ninhydrinin a mixture of methanol andacetic acid (100) (97:3) (1 in 100) on the plate, and heat at80℃ for 10 minutes: the spot other than the principal spot obtained from the sample solution is not more intense thanthe spot from the standard solution.
Loss on Drying <2.41> Not more than 0.3%(1 g, 105℃, 3 hours).
Residue on Ignition <2.44> Not more than 0.1%(1 g).
Assay Weigh accurately about 0.11 g of L-Serine, previously dried, dissolve in 3 mL of formic acid, add 50 mL of acetic acid (100), and titrate <2.50> with 0.1 mol/L perchloric acid VS (potentiometric titration). Perform a blank determination in the same manner, and make any necessary correction.
Each mL of 0.1 mol/L perchloric acid VS=10.51 mg of C3H7NO3
Containers and storage Containers-Tight containers.

USP39-NF34
DEFINITION L-Serine contains NLT 98.5% and NMT 101.5% of L-serine (C3H7NO3), calculated on the dried basis.
IDENTIFICATION
A. INFRARED ABSORPTION <197K>
ASSAY
PROCEDURE
Sample: 100mg of Serine
Blank: Mix 3mL of formic acid and 50mL of glacial acetic acid.
Titrimetric system
(See Titrimetry <541>)
Mode: Direct titration
Titrant: 0.1 N perchloric acid VS
Endpoint detection: Potentiometric
Analysis: Dissolve the Sample in 3mL of formic acid and 50mL of glacial acetic acid. Titrate with the Titrant.
Perform the Blank determination.
Calculate the percentage of serine (C3H7NO3) in the sample taken:
Result = {[(VS-VB) xNxF]/W} x100
VS= Titrant volume consumed by the Sample (mL)
VB= Titrant volume consumed by the Blank (mL)
N= actual normality of the Titrant (mEq/mL)
F= equivalency factor, 105.1mg/mEq
W= Sample weight (mg)
Acceptance criteria: 98.5%~101.5% on the dried basis
IMPURITIES
RESIDUEON IGNITION <281>: NMT 0.1%
CHLORIDEAND SULFATE, Chloride <221>
Standard solution: 0.50mL of 0.020 N hydrochloric acid
Sample: 0.73g of Serine
Acceptance criteria: NMT 0.05%
CHLORIDEAND SULFATE, Sulfate <221>
Standard solution: 0.10mL of 0.020 N sulfuric acid
Sample: 0.33g of Serine
Acceptance criteria: NMT 0.03%
IRON <241>: NMT 30ppm
Delete the following:
HEAVY METALS, Method I <231>: NMT 15ppm (Official 1-Jan-201)
RELATED COMPOUNDS
System suitability solution: 0.4mg/mL each of USP L-Serine RS and USP L-Methionine RS in 0.1 N hydrochloric acid
Standard solution: 0.05mg/mL of USP L-Serine RS in 0.1 N hydrochloric acid. [NOTE-This solution has a concentration equivalent to about 0.5% of that of the Sample solution.]
Sample solution: 10mg/mL of Serine in 0.1 N hydrochloric acid
Chromatographic system See Chromatography <621>, Thin-Layer Chromatography.)
Mode: TLC
Adsorbent: 0.25-mm layer of chromatographic silica gel mixture
Application volume: 5μL
Developing solvent system: Butyl alcohol, glacial acebutyl alcohol and 2N acetic acid (95:5)
System suitability
Suitability requirements: The chromatogram of the System suitability solution exhibits two clearly separated spots.
Analysis
Samples: System suitability solution, Standard solution, and Sample solution.
After air-drying the plate, spray with Spray reagent, and heat between 100° and 105° for 15 min. Examine the plate under white light.
Acceptance criteria: Any secondary spot of the Sample solution is not larger or more intense than the principal spot of the Standard solution.
Individual impurities: NMT 0.5%
Total impurities: NMT 2.0%
SPECIFIC TESTS
OPTICAL ROTATION, Specific Rotation <781S>
Sample solution: 100mg/mL in 2N hydrochloric acid
Acceptance criteria: +14.0° to +15.6°
LOSSON DRYING <731>: Dry a sample at 105℃ for 3 h: it loses NMT 0.2% of its weight.
ADDITIONAL REQUIREMENTS
ACKAGINGAND STORAGE: Preserve in well-closed containers.
USP REFERENCE STANDARDS <11>
USP L-Methionine RS
USP L-Serine RS

Advantages:

Sufficient Capacity: Sufficient facilities and technicians

Professional Service: One stop purchasing service

OEM Package: Custom package and label available

Fast Delivery: If within stock, three days delivery guaranteed

Stable Supply: Maintain reasonable stock    

Technical Support: Technology solution available

Custom Synthesis Service: Ranged from grams to kilos

High Quality: Established a complete quality assurance system

FAQ:

How to Purchase? Please contact Dr. Alvin Huang: sales@ruifuchem.com or alvin@ruifuchem.com 

15 Years Experience? We have more than 15 years of experience in the manufacture and export of a wide range of high quality pharmaceutical intermediates or fine chemicals.

Main Markets? Sell to domestic market, North America, Europe, India, Korea, Japanese, Australia, etc.

Advantages? Superior quality, affordable price, professional services and technical support, fast delivery.

Quality AssuranceStrict quality control system. Professional equipment for analysis include NMR, LC-MS, GC, HPLC, ICP-MS, UV, IR, OR, K.F, ROI, LOD, MP, Clarity, Solubility, Microbial limit test, etc.

SamplesMost products provide free samples for quality evaluation, shipping cost should be paid by customers.

Factory AuditFactory audit welcome. Please make an appointment in advance.

MOQ? No MOQ. Small order is acceptable.

Delivery Time? If within stock, three days delivery guaranteed.

TransportationBy Express (FedEx, DHL), by Air, by Sea.

Documents? After sales service: COA, MOA, ROS, MSDS, etc. can be provided.

Custom SynthesisCan provide custom synthesis services to best fit your research needs.

Payment TermsProforma invoice will be sent first after confirmation of order, enclosed our bank information. Payment by T/T (Telex Transfer), PayPal, Western Union, etc. 

63-91-2 - Risk and Safety:

Hazard Symbols Xi - Irritant
Risk Codes 36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description       S24/25 - Avoid contact with skin and eyes.
S36 - Wear suitable protective clothing.
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
WGK Germany 3
RTECS VT8100000
3
TSCA Yes
HS Code 2922509099

Application:

L-Serine (H-Ser-OH; Abbreviated Ser or S) (CAS: 56-45-1) is an amino acid, it is one of the proteinogenic amino acids. Its codons in the genetic code are UCU, UCC, UCA, UCG, AGU and AGC. By virtue of the hydroxyl group, serine is classified as a polar amino acid.
Function and Application of L-Serine Cas 56-45-1
1. L-Serine is used as a biochemical reagent and food additives; Used in biochemical research, organization culture medium preparation, medicine used for amino acids on nutrition medicine.
2. L-Serine is used in pharmaceutical field, L-Serine is widely used to configure the thirdgeneration compound amino acid infusion and nutritionalbsupplements, and for the synthesis of a variety of silk amino acid derivatives, such as cardiovascular, cancer, AIDS and genetic engineering of new drugs and other protected amino acids. Food and beverage Field, L-Serine can be used to sports drinks, amino acids diet drinks. Feed field, L-Serine can be used to animal feed, promote animal growth and development;
3. L-Serine is used as Nutritional supplement, in cosmetics as skin nutrition additive.
4. Available for biochemical and nutritional research purposes, but also can be used as synthetic ring serine raw materials
5. L-Serine has a wide range of uses in medicine. Serine promotes the metabolism of fats and fatty acids and helps maintain the immune system.
6. L-Serine is also used as a dietary supplement where it can aid improved memory function and in personal care products where it helps with the production of new skin cells.
7. L-Serine has been used in the preparation of Tris-BSAN buffer for homogenization. It has also been used for quantitative analysis of excretion of polypeptides in normal urine.
8. L-Serine is used in the synthesis of purines and pyrimidines as antibacterial/antifungal agents, as well as acting as a proteinogenic compound.
9. L-Serine is classified as a non-essential amino acid. It is used as a cell culture media component and raw material for the commercial biomanufacture of therapeutic recombinant proteins and monoclonal antibodies.
10. L-Serine through phosphorylation-hydroxy derivative can be issued after the important physiological functions of P serine is a major component of phospholipids;
11. L-Serine with a stable pH value of the role of eye drops, eye drops and non-irritating;
12. L-Serine is an important natural moisturizing factor (NMF) is one of stratum corneum to maintain the primary role of water, L-Serine is the key to advanced cosmetic additives. 

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