PHR1959

Salbutamol Impurity B

Pharmaceutical Secondary Standard; Certified Reference Material

Manufacturer: Supelco

CAS Number: 96948-64-0

Synonym(S): (1RS)-2-[(1,1-Dimethylethyl)amino]-1-(4-hydroxyphenyl)ethanol, Albuterol Related Compound I, 2-tert-Butylamino-1-(4-hydroxyphenyl)ethanol

Select a Size

Pack Size SKU Availability Price
50 MG PHR1959-50-MG In Stock ₹ 69,074.33

PHR1959 - 50 MG

₹ 69,074.33

In Stock

Quantity

1

Base Price: ₹ 69,074.33

GST (18%): ₹ 12,433.379

Total Price: ₹ 81,507.709

grade

certified reference materialpharmaceutical secondary standard

Quality Level

300

Agency

traceable to BP 852traceable to Ph. Eur. Y0000030

form

powder

CofA

current certificate can be downloaded

packaging

pkg of 50 mg

application(s)

pharmaceutical

storage temp.

2-8°C

InChI

1S/C12H19NO2/c1-12(2,3)13-8-11(15)9-4-6-10(14)7-5-9/h4-7,11,13-15H,8H2,1-3H3

InChI key

JOGFUYPGDLRKHD-UHFFFAOYSA-N

Other Options

Image Product Name Manufacturer Price Range
50-186-9897
Sigma Aldrich Fine Chemicals Biosciences Salbutamol impurity B European Pharmacopoeia (EP) Reference Standard | 96948-64-0 |
Sigma Aldrich Fine Chemicals Biosciences ₹ 23,582.90
11-101-5984
Salbutamol Impurity B Pharmaceutical Secondary Standard, MilliporeSigma™ Supelco™
MilliporeSigma Supelco ₹ 72,640.44
BP852
Salbutamol impurity B
Sigma Aldrich ₹ 21,401.03
Y0000030
Salbutamol impurity B
Sigma Aldrich ₹ 16,107.60
1012564
Albuterol Related Compound I
Sigma Aldrich ₹ 1,33,396.48
CS-0534170
4-(2-(tert-Butylamino)-1-hydroxyethyl)phenol Salbutamol Impurity
ChemScene --
AX44460
96948-64-0 | 4-(2-(tert-Butylamino)-1-hydroxyethyl)phenol
A2B Chem ₹ 95,228.28

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Description

  • General description: Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards
  • Application: Salbutamol Impurity B Analysis in Pharmaceutical Products: Utilizing advanced chromatographic techniques, researchers have developed validated methods for the precise identification and quantification of Salbutamol Impurity B in pharmaceutical formulations. This critical quality control measure ensures the safety and efficacy of bronchodilator medications, adhering to stringent regulatory standards (Kondra et al., 2023).Development of Analytical Standards for Salbutamol Impurity B: The quantification of Salbutamol Impurity B using achiral supercritical fluid chromatography represents a significant advancement in the field of pharmaceutical impurities identification. This method provides a robust, efficient, and reproducible approach for monitoring the stability and purity of salbutamol-based therapies, contributing to enhanced patient safety (Dispas et al., 2017).Research on Salbutamol Degradation Products: A stability-indicating RP-HPLC method has been developed for the simultaneous determination of Salbutamol Impurity B and other related substances in nasal solutions. This method is crucial for understanding the degradation pathways of salbutamol, thereby assisting in the development of more stable and effective bronchodilator formulations (Kasawar & Farooqui, 2010).
  • Analysis Note: These secondary standards offer multi-traceability to the USP, EP and BP primary standards, where they are available.
  • Other Notes: This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.
  • Footnote: To see an example of a Certificate of Analysis for this material enter LRAB3289 in the Documents slot below. This is an example certificate only and may not be the lot that you receive.
  • Recommended products: Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

SAFETY INFORMATION

Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Precautionary Statements

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Pharmaceutical Secondary Standard; ...


grade:
certified reference materialpharmaceutical secondary standard

Quality Level:
300

Agency:
traceable to BP 852traceable to Ph. Eur. Y0000030

form:
powder

CofA:
current certificate can be downloaded

packaging:
pkg of 50 mg

application(s):
pharmaceutical

storage temp.:
2-8°C

InChI:
1S/C12H19NO2/c1-12(2,3)13-8-11(15)9-4-6-10(14)7-5-9/h4-7,11,13-15H,8H2,1-3H3

InChI key:
JOGFUYPGDLRKHD-UHFFFAOYSA-N

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current certificate can be downloaded

packaging:
pkg of 50 mg

application(s):
pharmaceutical

storage temp.:
2-8°C

InChI:
1S/C13H19NO3/c1-13(2,3)14-7-12(17)9-4-5-11(16)10(6-9)8-15/h4-6,8,12,14,16-17H,7H2,1-3H3

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1S/C20H27NO3/c1-20(2,3)21-12-18(23)16-9-10-19(17(11-16)13-22)24-14-15-7-5-4-6-8-15/h4-11,18,21-23H,12-14H2,1-3H3

InChI key:
__