Quick Search

PRODUCTS

1-METHYL-2-PYRROLIDINONE (N-METHYL-2-PYRROLIDINONE)

1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is an organic compound consisting of a 5-membered lactam. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is a colorless liquid, although impure samples can appear yellow. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is miscible with water and with most common organic solvents. 

CAS:    872-50-4
MF:    C5H9NO
MW:    99.13
EINECS:    212-828-1

1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) also belongs to the class of dipolar aprotic solvents such as dimethylformamide and dimethyl sulfoxide. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is used in the petrochemical, polymer and battery industries as a solvent, exploiting its nonvolatility and ability to dissolve diverse materials (including polyvinylidene difluoride, PVDF).
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is a powerful, aprotic solvent with high solvency, and low volatility. 
This colorless, high boiling, high flash point and low vapor pressure liquid carries a mild amine-like odor. 

1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) has high chemical and thermal stability and is completely miscible with water at all temperatures. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) can serve as a co-solvent with water, alcohols, glycol ethers, ketones, and aromatic/chlorinated hydrocarbons. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is both recyclable by distillation and readily biodegradable. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is not found on the Hazardous Air Pollutants (HAPs) list of the 1990 Clean Air Act Amendments.

1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is a solvent used in a variety of industries and applications, such as paint and coating removal, petrochemical processing, engineering plastics coatings, agricultural chemicals, electronic cleaning and industrial/domestic cleaning.
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is a colorless liquid with a mild, fishy odor. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is used as a solvent in chemical processing, in paint thinners, and in pharmaceutical applications.
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) has a molecular formula of C5H9NO, and it is a colorless to light yellow transparent liquid with a slight ammonia odor. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone)'s boiling point is 204℃, flash point is 91℃, chroma HaZen≤25, refractive index N20D 1.468-1.471, density is 1.032-1.035. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is miscible in water at any ratio, it is soluble in ethanol, acetone, esters, halogenated hydrocarbons, aromatic hydrocarbons and other organic solvents, and 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) can completely mix with practically all solvents.

1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) appears as a clear colorless liquid with a "fishlike" odor. 
Denser than water. 
Flash point 199°F. 
Contact may irritate skin, eyes and mucous membranes. 
May be toxic by ingestion.
A clear colorless liquid with a fish-like odor.

1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is a member of the class of pyrrolidine-2-ones that is pyrrolidin-2-one in which the hydrogen attached to the nitrogen is replaced by a methyl group. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) has a role as a polar aprotic solvent. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is a N-alkylpyrrolidine, a lactam and a member of pyrrolidin-2-ones.
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is under investigation for the treatment of Multiple Myeloma.

1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) Chemical Properties
Melting point: -24 °C (lit.)
Boiling point: 202 °C (lit.) 81-82 °C/10 mmHg (lit.)
Density: 1.028 g/mL at 25 °C (lit.)
Vapor density: 3.4 (vs air)
Vapor pressure: 0.29 mm Hg ( 20 °C)
Refractive index: n20/D 1.479
Fp: 187 °F
Storage temp.: Store at +5°C to +30°C.
Solubility: ethanol: miscible0.1ML/mL, clear, colorless (10%, v/v)
Form: Liquid
pka: -0.41±0.20(Predicted)
Color: ≤20(APHA)
PH: 8.5-10.0 (100g/l, H2O, 20℃)
Odor: Slight amine odor
PH Range: 7.7 - 8.0
Explosive limit: 1.3-9.5%(V)
Water Solubility: >=10 g/100 mL at 20 ºC
Sensitive: Hygroscopic
λmax: 283nm(MeOH)(lit.)
Merck: 14,6117
BRN: 106420
Stability: Stable, but decomposes upon exposure to light. 
Combustible. Incompatible with strong oxidizing agents, strong acids, reducing agents, bases.
InChIKey: SECXISVLQFMRJM-UHFFFAOYSA-N
LogP: -0.46 at 25℃
CAS DataBase Reference: 872-50-4(CAS DataBase Reference)
NIST Chemistry Reference: 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) (872-50-4)
EPA Substance Registry System: 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) (872-50-4)

1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is a colourless or light yellow liquid with an amine odour. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) can undergo a number of chemical reactions even though it is accepted as a stable solvent. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is resistant to hydrolysis under neutral conditions, but strong acid or base treatment results in ring opening to 4-methyl aminobutyric acid. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) can be reduced to 1-methyl pyrrolidine with borohydride. 
Treatment with chlorinating agents results in amide formation,an intermediate which can undergo further substitution, while treatment with amyl nitrate yields the nitrate. 
Olefins can be added to the 3 position by treatment first with oxalic esters, then with appropriate aldehyes (Hort and Anderson 1982).

Preparation
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is produced industrially by a typical ester-to-amide conversion, by treating butyrolactone with methylamine. 
Alternative routes include the partial hydrogenation of N-methylsuccinimide and the reaction of acrylonitrile with methylamine followed by hydrolysis. 
About 200,000 to 250,000 tons are produced annually.

Applications
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is used to recover certain hydrocarbons generated in the processing of petrochemicals, such as the recovery of 1,3-butadiene and acetylene. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is used to absorb hydrogen sulfide from sour gas and hydrodesulfurization facilities. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone)'s good solvency properties have led to NMP's use to dissolve a wide range of polymers. 
Specifically, 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is used as a solvent for surface treatment of textiles, resins, and metal coated plastics or as a paint stripper. 

1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is also used as a solvent in the commercial preparation of polyphenylene sulfide. 
In the pharmaceutical industry, 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is used in the formulation for drugs by both oral and transdermal delivery routes.
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is also used heavily in lithium ion battery fabrication, as a solvent for electrode preparation, because NMP has a unique ability to dissolve polyvinylidene fluoride binder. 
Due to 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone)'s toxicity and high boiling point, there is much effort to replace it in battery manufacturing with other solvent(s), like water.

1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is an excellent solvent, widely used as an extractant for aromatic extraction, lubricating oil refining, acetylene concentration, synthesis gas desulfurization, etc. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is also used for industrial cleaning and other purposes. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is an excellent extraction solvent. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is widely used as an extractant in the process of aromatics extraction, acetylene concentration, butadiene separation and synthesis gas desulfurization. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is also a solvent in the production of pesticides, engineering plastics, coatings, synthetic fibers, integrated circuits, etc. Industrial detergents, dispersants, dyes, lubricants antifreeze, etc. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) has low toxicity, and the oral LD50 for rats is 7ml/kg. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is widely used in solvents such as high-grade lubricating oil refining, polymer synthesis, insulating materials, pesticides, pigments and cleaning agents.

1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is a polar solvent that is used in organic chemistry and polymer chemistry. 
Large scale applications include the recovery and purification of acetylenes, olefins, and diolefins, gas purification, and aromatics extraction from feedstocks.
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is a versatile industrial solvent. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is currently approved for use only in veterinary pharmaceuticals. 
The determination of the disposition and metabolism of 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) in the rat will contribute toward understanding the toxicology of this exogenous chemical which man may likely be exposed to in increasing amounts.
Solvent for high-temperature resins; petrochemical processing, in the microelectronics fabrication industry, dyes and pigments, industrial and domestic cleaning compounds; agricultural and pharmaceutical formulations.

Health hazards
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is an agent that causes the production of physical defects in the developing embryo.
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) also is a reproductive toxin, a chemical that is toxic to the reproductive system, including defects in the progeny and injury to male or female reproductive function. 
Reproductive toxicity includes developmental effects.
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) can be absorbed into the body by inhalation, through the skin and by ingestion. 
When people are exposed to 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone), rapid, irregular respiration, shortness of breath, decreased pain reflex, and slight bloody nasal secretion are possible.
Inhalation can result in headaches and exposure on skin can result in redness and pain. 
When ingested 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) will cause a burning sensation in the throat and chest. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) also can cause an acute solvent syndrome.

Metabolism    
Male Sprague-Dawley rats were given a single intraperitoneal injection (45 mg/kg) of radiolabeled 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone). 
Plasma levels of radioactivity and compound were monitored for six hours and the results suggested a rapid distribution phase which was followed by a slow elimination phase. 
The major amount of label was excreted in the urine within 12 hours and accounted for approximately 75% of the labelled dose. 
Twenty-four hours after dosage, cumulative excretion (urine) was approximately 80% of the dose. 
Both ring- and methyl-labeled species were used, as well as both [14C]- and [3H]-labeled 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone). 

The initial labeled ratios were maintained during the first 6 hours after dosage. 
After 6 hours, the liver and intestines were found to contain the highest accumulations of radioactivity, approximately 2-4% of the dose. 
Little radioactivity was noted in the bile or respired air. 
High performance liquid chromatography of urine showed the presence of one major and two minor metabolites. 
The major metabolite (70-75% of the administered radioactive dose) was analyzed by liquid chromatography-mass spectrometry and gas chromatography-mass spectrometry and was proposed to be a 3- or 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone).

Biological aspects
In rats, 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is absorbed rapidly after inhalation, oral, and dermal administration, distributed throughout the organism, and eliminated mainly by hydroxylation to polar compounds, which are excreted via urine. 
About 80% of the administered dose is excreted as 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) and 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) metabolites within 24 hours. 
A probably dose dependent yellow coloration of the urine in rodents is observed. 
The major metabolite is 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone).

Studies in humans show comparable results. 
Dermal penetration through human skin has been shown to be very rapid. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is rapidly biotransformed by hydroxylation to 5-hydroxy-N-methyl-2-pyrrolidone, which is further oxidized to N-methylsuccinimide; this intermediate is further hydroxylated to 2-hydroxy-N-methylsuccinimide. 
These metabolites are all colourless. 
The excreted amounts of NMP metabolites in the urine after inhalation or oral intake represented about 100% and 65% of the administered doses, respectively. 

1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) has a low potential for skin irritation and a moderate potential for eye irritation in rabbits. 
Repeated daily doses of 450 mg/kg body weight administered to the skin caused painful and severe haemorrhage and eschar formation in rabbits. 
These adverse effects have not been seen in workers occupationally exposed to pure 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone), but they have been observed after dermal exposure to 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) used in cleaning processes. 
No sensitization potential has been observed.

Carcinogenicity    
Rats were exposed to 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) vapor at 0, 0.04, or 0.4 mg/L for 6 h/day, 5 days/week for 2 years.
Male rats at 0.4 mg/L showed slightly reduced mean body weight. 
No life-shortening toxic or carcinogenic effects were observed in rats exposed for 2 years to either 0.04 or 0.4mg/L of 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone). 
By the dermal route, a group of 32 mice received an initiation dose of 25mg of 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) followed 2 weeks later by applications of the tumor promoter phorbol myristate acetate, three times a week, for more than 25 weeks. 
Dimethylcarbamoyl chloride and dimethylbenzanthracene served as positive controls. 
Although the 1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) group had three skin tumors, this response was not considered significant when compared with that of the positive controls.

Contact allergens    
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is an aprotic solvent with a wide range of applications: petrochemical processing, surface coating, dyes and pigments, industrial and domestic cleaning compounds, and agricultural and pharmaceutical formulations. 
1-Methyl-2-pyrrolidinone (N-Methyl-2-pyrrolidinone) is mainly an irritant, but it can cause severe contact dermatitis due to prolonged contact.

Synonyms
1-METHYL-2-PYRROLIDINONE
872-50-4
N-Methylpyrrolidone
N-Methyl-2-pyrrolidone
1-methylpyrrolidin-2-one
Methylpyrrolidone
1-Methyl-2-pyrrolidone
N-Methyl-2-pyrrolidinone
M-Pyrol
N-Methylpyrrolidinone
1-Methylpyrrolidinone
1-Methylpyrrolidone
Methyl pyrrolidone
n-methyl-pyrrolidone
2-Pyrrolidinone, 1-methyl-
1-Methyl-5-pyrrolidinone
1-Methylazacyclopentan-2-one
N-methylpyrrolidin-2-one
NMP
N-Methyl-gamma-butyrolactam
N-methyl pyrrolidone
1-methylpyrrolidine-2-one
N-methyl pyrrolidinone
Methyl-2-pyrrolidinone
1-methyl-2-pyrrolidon
Methylpyrrolidinone
2-Pyrrolidinone, methyl-
Methylpyrrolidone [NF]
N-Methylpyrrolid-2-one
2687-44-7
N-Methyl-alpha-pyrrolidone
NSC 4594
Agsolex 1
N-Methyl-alpha-pyrrolidinone
51013-18-4
DTXSID6020856
NSC-4594
MFCD00003193
JR9CE63FPM
1-methyl-pyrrolidin-2-one
N-Methyl-.alpha.-pyrrolidone
CHEMBL12543
N-Methyl-.gamma.-butyrolactam
CHEBI:7307
N-Methyl-.alpha.-pyrrolidinone
1-Methyl-2-pyrrolidinone, anhydrous
1-Methyl-2-pyrrolidinone, HPLC Grade
N 0131
26876-92-6
DTXCID60856
pharmasolve
N-Methylpyrrolidon
CAS-872-50-4
CCRIS 1633
N-methyl-pyrrolidinone
Methylpyrrolidone, N-
HSDB 5022
Pyrrolidinone, methyl-
N-Methyl-2-pyrrolidon
1-methyl-2-pyrolidone
EINECS 212-828-1
UNII-JR9CE63FPM
N-methyl-pyrrolidin-2-one
1-Methyl-2-pyrrolidinone, puriss. p.a., >=99.0% (GC)
Micropure ultra
AI3-23116
N-methylpyrolidone
N-methypyrrolidone
Max-1 peptide
Pyrol M
N-methylpirrolidone
1methylpyrrolidinone
n-methyl pyrrolidon
n-methylbutyrolactam
N-methy pyrrolidone
N-methyl-pyrolidone
N-methyl-pyrrolidon
N-methylpyrolidinone
1-methylpyrolidinone
Microposit 2001
n-methylpyrollidinone
N-Methylpyrrolidione
N-methlypyrrolidinone
N-methyl pirrolidone
N-methyl pyrollidone
N-methyl-pyrollidone
N-methylpyrrolidone-
NMP,SP Grade
1-methyl pyrrolidone
1-methyl-pyrrolidone
methyl-2-pyrrolidone
N-methy pyrrolidinone
N-methyl pyrolidinone
N-methyl-pyrolidinone
N-methyl- pyrrolidone
N-methylpyrro-lidinone
N-methylpyrroli-dinone
N-methylpyrrolidin-one
1-methyl-2pyrrolidone
1-methyl2-pyrrolidone
1methyl-2-pyrrolidone
1-methyl pyrrolidinone
1-methyl-pyrrolidinone
methylpyrrolidin-2-one
N-methy-2-pyrrolidone
N-methyl 2-pyrolidone
N-methyl-2-pyrolidone
3p1d
N-methyl 2-pyrrolidone
N-methyl-2-pyrollidone
1-methyl-2-pirrolidone
1-methyl-2-pyroldinone
1-methylpyrrolid-2-one
1methyl-2-pyrrolidinone
n-methylpyrrolidine-2one
N-methyl-2-pyrolidinone
N-methyl-2-pyrrolidinon
N-methylpyrolidin-2-one
1-methy-2-pyrrolidinone
1-methyl-2-pyrolidinone
N-methyl 2-pyrrolidinone
N-methyl-2-pyrollidinone
N-methyl-pyrrolid-2-one
N-methylpyrollidin-2-one
1 -methyl-2-pyrrolidone
1-methyl 2-pyrrolidinone
1-methyl-2-pyrollidinone
1-methyl-pyrrolin-2-one
N-Methylpyrrolidone-(2)
NMP, N-Methylpyrrolidone
1-Methyl-pyrrolidin-2one
N-methylpyrrolidine-2-one
WLN: T5NVTJ A
N-methyl -2-pyrrolidinone
1 -methyl-2-pyrrolidinone
1-methyl -2-pyrrolidinone
1-methyl-2- pyrrolidinone
EC 212-828-1
2-Pyrrolidone, 1-methyl-
1-methyl-pyrrolidine-2-one
1-N-methyl-2-pyrrolidinone
N-methyl-pyrrolidin -2-one
30207-69-3
1-Methylazacyclopentane-2-one
GTPL9520
METHYL PYRROLIDONE [II]
1-Methyl-2- pyrrolidin-2-one
1-METHYLPYRROLIDONE [MI]
METHYL PYRROLIDONE [INCI]
NSC4594
METHYLPYRROLIDONE [USP-RS]
HY-Y1275
N-METHYLPYRROLIDONE [MART.]
ZINC3860621
Tox21_202350
Tox21_300097
1-Methyl-2-pyrrolidinone, 99.5%
BDBM50353587
N-Methyl pyrrolidon (Peptide Grade)
N-METHYLPYRROLIDONE [USP-RS]
s6282
STL183295
N-Methyl-2-pyrrolidinone ACS reagent
AKOS000120930
1-Methyl-2-pyrrolidinone, BioSolv(R)
DB12521
SL 1332
1-Methyl-2-pyrrolidone, Reagent, ACS
1-METHYL-2-PYRROLIDINONE [HSDB]
NCGC00247902-01
NCGC00247902-02
NCGC00253935-01
NCGC00259899-01
BP-31156
N-METHYLPYRROLIDONE [EP MONOGRAPH]
1-Methyl-2-pyrrolidone (Low water content)
AM20110252
CS-0017258
FT-0608052
FT-0672137
FT-0698122
FT-0700571
M0418
M3055
1-Methyl-2-pyrrolidinone, analytical standard
1-Methyl-2-pyrrolidinone, anhydrous, 99.5%
1-Methyl-2-pyrrolidinone, for HPLC, >=99%
1-Methyl-2-pyrrolidinone, for synthesis, 99%
D78116
M 0418
Q33103
Residual Solvent Class 2 - N-Methylpyrrolidone
1-Methyl-2-pyrrolidinone, ReagentPlus(R), 99%
1-Methyl-2-pyrrolidinone, Spectrophotometric Grade
2-PYRROLIDONE,1-METHYL MFC5 H9 N1 O1
A842053
1-Methyl-2-pyrrolidinone, ACS reagent, >=99.0%
2,5-Dichloro-4,6-dimethyl pyridine-3-carbonitrile
J-504921
J-803017
1-Methyl-2-pyrrolidinone, biotech. grade, >=99.7%
1-Methyl-2-pyrrolidinone, Electronic/Cleanroom Grade
1-Methyl-2-pyrrolidinone, p.a., ACS reagent, 99%
1-Methyl-2-pyrrolidone, anhydrous, water 40ppm max.
1-Methyl-2-pyrrolidinone, SAJ first grade, >=98.0%
Z104478382
1-Methyl-2-pyrrolidinone, spectrophotometric grade, >=99%
1-Methyl-2-pyrrolidinone, Vetec(TM) reagent grade, 98%
1-Methyl-2-pyrrolidinone, for metal speciation analysis, >=99.0% (GC)
Methylpyrrolidone, United States Pharmacopeia (USP) Reference Standard
N-Methylpyrrolidone, Pharmaceutical Secondary Standard; Certified Reference Material

  • Share !
E-NEWSLETTER