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97085

Supelco

Benzylidene camphor sulfonic acid

analytical standard

Synonym(s):

α-(2-Oxoborn-3-ylidene)-toluene-4-sulphonic acid, 3-Benzylidenecamphor-4′-sulphonic acid, 4′-Sulfo-3-benzylidenecamphor, 4-[(4,7,7-Trimethyl-3-oxobicyclo[2.2.1]hept-2-ylidene)methyl]benzenesulfonic acid, p-[(2-Oxo-3-bornylidene)methyl]benzenesulfonic acid, BCSA

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About This Item

Empirical Formula (Hill Notation):
C17H20O4S
CAS Number:
Molecular Weight:
320.40
Beilstein/REAXYS Number:
14648450
UNSPSC Code:
85151701
NACRES:
NA.24

grade

analytical standard

Quality Level

assay

≥97.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

impurities

≤8.0% water (calc. from elemental analysis)

application(s)

environmental

format

neat

SMILES string

CC1(C)[C@@H]2CC[C@]1(C)C(/C2=C\C3=CC=C(S(=O)(O)=O)C=C3)=O

InChI

1S/C17H20O4S/c1-16(2)14-8-9-17(16,3)15(18)13(14)10-11-4-6-12(7-5-11)22(19,20)21/h4-7,10,14H,8-9H2,1-3H3,(H,19,20,21)/b13-10-

InChI key

KKJKXQYVUVWWJP-RAXLEYEMSA-N

General description

Benzylidene camphor sulfonic acid (BCSA) is an organic ultraviolet absorbing compound used primarily in cosmetics (sunscreens, lipsticks, shampoos and hair sprays).

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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.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Organic UV filters and their photodegradates, metabolites and disinfection by-products in the aquatic environment.
Diaz-Cruz MS, et al.
TrAC, Trends in Analytical Chemistry, 27(10), 873-887 (2008)

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