제약 등급 연어 PN CAS 9007-49-2

Salmon-derived Sodium DNA raw material with an average molecular weight of ≥1,000 kDa. Defined specifications cover assay, protein, residual ethanol, microbiological quality and bacterial endotoxin.

  • CAS: 9007-49-2
  • 분자식: C15H31N3O13P2
  • Molecular Weight: 523.37
  • EINECS:2017-001-1
  • Average Molecular Weight: ≥1,000 kDa
  • Assay: ≥95.0%
  • Protein Content: <1.0%
  • Bacterial Endotoxin: <0.5 EU/mg
  • 보관 기간: 2년

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NewPN-P® 제약 등급 연어 PN

Renew supplies NewPN-P® pharmaceutical grade Salmon PN, identified as Sodium DNA under CAS 9007-49-2. This ≥1,000 kDa raw material is supplied for formulation development, analytical evaluation and material qualification.

The grade combines an average molecular-weight specification of ≥1,000 kDa with defined limits for assay, protein, ethanol residue, heavy metals, bacterial endotoxin and microbiological quality. These parameters give procurement, R&D and QA teams a clearer basis for comparison than the terms PN, PDRN or salmon DNA alone.

NewPN-P® is a raw material for further development and qualification. It is not a finished pharmaceutical or medical-aesthetic product. Finished-product requirements depend on the intended use, route, formulation, manufacturing process and destination market.

신속 조달 정보

항목 상세 정보
Brand / grade NewPN-P® 제약 등급 연어 PN
Product identity Sodium DNA / salmon-derived polynucleotide raw material
CAS 번호 9007-49-2
모양 흰색 또는 회백색 분말 또는 섬유질 고체
용해성 물에 약간 용해됨
평균 분자량 ≥1,000 kDa
분석 ≥95.0%
단백질 함량 <1.0%
박테리아 내독소 <0.5 EU/mg
표준 포장 50 g/bottle, 100 g/bottle, 1 kg/bag
유통기한 2 years
Quality documentation Example COA available; request the current documents required for qualification
샘플, 최소 주문 수량(MOQ) 및 납기 현재 견적과 확인되었습니다

The table presents the acceptance criteria shown in the available product COA. Actual batch results are reported in the applicable lot-specific COA. Buyers with additional test, limit or method requirements can include them in the technical enquiry.

시험 문항 사양
모양 흰색 또는 회백색 분말 또는 섬유질 고체
용해성 물에 약간 용해됨
신원 확인 UV absorbance ratio at 260/280 nm: 1.5–2.0
pH 5.0–9.0
평균 분자량 ≥1,000 kDa
단백질 함량 <1.0%
건조 시 손실 ≤20.0%
중금속 ≤10 μg/g
투과율 ≥96.0%
Ethanol residue <0.5%
박테리아 내독소 <0.5 EU/mg
총 호기성 미생물 수 NMT 100 CFU/g
Total molds and yeasts NMT 100 CFU/g
황색포도상구균 부정적
슈도모나스 아에루기노사 부정적
대장균 부정적
분석 ≥95.0%

Key Quality Attributes of NewPN-P®

Renew specifies NewPN-P® at an average molecular weight of ≥1,000 kDa. This identifies it as the higher-molecular-weight PN grade within Renew’s Sodium DNA portfolio.

Because Sodium DNA is polymeric, the reported value represents an average rather than one fixed molecular size. Include any required molecular-weight distribution, reporting basis or analytical method in the technical enquiry.

The assay specification is ≥95.0%. Protein is controlled separately at <1.0%, while ethanol residue, loss on drying and heavy metals each have their own acceptance limits. This separation helps buyers compare the complete quality profile instead of treating assay as the only purchasing criterion.

The specification includes bacterial endotoxin below 0.5 EU/mg, limits for total aerobic microorganisms and molds and yeasts, and absence criteria for three named microorganisms.

The assay specification is ≥95.0%. Protein is controlled separately at <1.0%, while ethanol residue, loss on drying and heavy metals each have their own acceptance limits. This separation helps buyers compare the complete quality profile instead of treating assay as the only purchasing criterion.

Comparing NewPN-P® and NewPDRN-P®

Renew supplies NewPN-P® and NewPDRN-P® as separate commercial grades. Within Renew’s current product portfolio, a key stated specification difference is average molecular weight.

Renew Grade 평균 분자량 Selection Context
NewPN-P® 제약 등급 연어 PN ≥1,000 kDa Projects specifying Renew’s higher-molecular-weight PN grade
NewPDRN-P® 제약 등급 연어 PDRN ≤1,000 kDa Projects specifying Renew’s lower-molecular-weight PDRN grade

These limits define Renew’s commercial grades. They are not universal definitions used by every supplier. Compare the current specification, analytical method, sample behavior and applicable batch documentation when assessing alternatives.

For a lower-molecular-weight option, review Renew’s NewPDRN-P® Pharmaceutical Grade Salmon PDRN.

Applications of NewPN-P® Salmon PN

Pharmaceutical Formulation Development

NewPN-P® can be considered during pharmaceutical formulation and analytical development when salmon-derived Sodium DNA with an average molecular weight of ≥1,000 kDa is required. Its defined assay, protein, residual ethanol, endotoxin and microbiological specifications support initial material screening. Confirm compatibility, processing, stability and route-specific requirements before scale-up.

Professional Medical-Aesthetic Product Development

NewPN-P® may be assessed for professional medical-aesthetic product development where higher-molecular-weight salmon PN is specified. Evaluate the product format, use level, processing method, stability and destination-market requirements. Pharmaceutical grade describes the raw-material specification; it does not establish finished-product approval or suitability for injection or implantation.

Medical-Device Development Requirements

For projects following a medical-device pathway, use the NewPN-P® specification and example COA only for initial material screening. Submit the intended purpose, target market, material function, contact type and duration, required tests and document list with the enquiry. Finished-product classification, sterility, biocompatibility, safety and performance must be established separately.

품질 및 배치 문서

For an order, use the lot-specific COA issued for the applicable batch. Request current supporting documents according to the intended product, destination country and internal qualification requirements.

Include any additional test, standard or analytical-method requirements in the enquiry for technical review.

포장 및 보관

  • NewPN-P® is available in 50 g/bottle, 100 g/bottle and 1 kg/bag packaging.
  • The stated shelf life is two years.
  • Follow the storage conditions on the current product label and current product documents.

자주 묻는 질문

Yes. Provide the intended application, required sample quantity and document needs. Request the COA applicable to any commercial lot under consideration. Current sample terms are confirmed with the quotation.

MOQ and lead time are confirmed with the current quotation. They may vary with quantity, packaging, documentation and destination.

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