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4-AMINOBENZOIC-2, 3, 5, 6-D4 ACID is a deuterated form of 4-aminobenzoic acid, also known as para-aminobenzoic acid (PABA), which is an organic compound commonly used in the production of sunscreen and other cosmetic products due to its ability to absorb ultraviolet (UV) radiation. This specific form of PABA is labeled with deuterium, a non-radioactive isotope of hydrogen, making it a valuable tracer in pharmaceutical research and biochemical studies for tracking the metabolic pathways of the parent compound.

350820-01-8

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350820-01-8 Usage

Uses

Used in Pharmaceutical Research:
4-AMINOBENZOIC-2, 3, 5, 6-D4 ACID is used as a tracer in pharmaceutical research for tracking the metabolic pathways of the parent compound, PABA. Its deuterated form allows for the study of biochemical processes and interactions with other compounds in the body.
Used in Biochemical Studies:
In biochemical studies, 4-AMINOBENZOIC-2, 3, 5, 6-D4 ACID is used as a tracer to investigate the metabolic fate of PABA and its role in various biological processes. This helps researchers understand the compound's behavior and potential applications in medicine and other fields.
Used in Cosmetics Industry:
4-AMINOBENZOIC-2, 3, 5, 6-D4 ACID is used as an ingredient in the production of sunscreen and other cosmetic products for its ability to absorb ultraviolet (UV) radiation, providing protection against harmful UV rays and reducing the risk of skin damage and skin cancer.
Used in Scientific Research:
4-AMINOBENZOIC-2, 3, 5, 6-D4 ACID is used in scientific research across different industries due to its unique properties as a deuterated compound. Its ability to serve as a tracer allows for the investigation of various biological and chemical processes, contributing to the advancement of knowledge in multiple fields.

Check Digit Verification of cas no

The CAS Registry Mumber 350820-01-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,0,8,2 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 350820-01:
(8*3)+(7*5)+(6*0)+(5*8)+(4*2)+(3*0)+(2*0)+(1*1)=108
108 % 10 = 8
So 350820-01-8 is a valid CAS Registry Number.

350820-01-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-AMINOBENZOIC-2, 3, 5, 6-D4 ACID

1.2 Other means of identification

Product number -
Other names Fourrine D-d4

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:350820-01-8 SDS

350820-01-8Relevant academic research and scientific papers

Deuterium-Labeled Precursor Feeding Reveals a New pABA-Containing Meroterpenoid from the Mango Pathogen Xanthomonas citri pv. mangiferaeindicae

Saleh, Hesham,Petras, Daniel,Mainz, Andi,Kerwat, Dennis,Nalbantsoy, Ayse,Erzurumlu, Yalcin,Süssmuth, Roderich D.

, p. 1532 - 1537 (2016/07/06)

A new para-aminobenzoic-acid-containing natural product from the mango pathogenic organism Xanthomonas citri pv. mangiferaeindicae is described. By means of stable isotope precursor feeding combined with nontargeted LC-MS/MS, the generated spectra were cl

Synthesis of deuterium-labelled isotopomer of deferasirox

Havaldar, Freddy H.,Dabholkar, Bhushan Vasant,Mule, Ganesh Baban,Kulkarni, Suhas

, p. 163 - 165 (2015/04/27)

A d4-labeled isotopomer of deferasirox was synthesized as internal standard for use in a LC/mass spectroscopy (MS)/MS method developed for the simultaneous quantitative determination of deferasirox in human serum. d4-deferasirox was synthesized from d8-toluene.

Synthesis, characterization and applicability of three isotope labeled azobenzene photoswitches

Pfister, Rolf,Ihalainen, Janne,Hamm, Peter,Kolano, Christoph

experimental part, p. 3508 - 3517 (2009/02/05)

We describe a short, efficient approach for the synthesis of three novel isotope labeled azobenzene photoswitches. The synthesis is based on commercially available fully isotope labeled precursors. The target molecules have been obtained in good yields, c

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