ChemicalBook > CAS DataBase List > o-Phthalaldehyde

o-Phthalaldehyde

Product Name
o-Phthalaldehyde
CAS No.
643-79-8
Chemical Name
o-Phthalaldehyde
Synonyms
OPA;OPD;PHTHALALDEHYDE;PHTHALDIALDEHYDE;1,2-BENZENEDICARBOXALDEHYDE;O-PHTHALDIALDEHYDE;ORTHO-PHTHALALDEHYDE;1,2-PHTHALIC DICARBOXALDEHYDE;Phthaldialdehy;O-PHTHALDEHYDE
CBNumber
CB6731197
Molecular Formula
C8H6O2
Formula Weight
134.13
MOL File
643-79-8.mol
More
Less

o-Phthalaldehyde Property

Melting point:
55-58 °C(lit.)
Boiling point:
83-84 °C (0.7501 mmHg)
Density 
1.13
bulk density
530kg/m3
vapor pressure 
0.56Pa at 25℃
refractive index 
1.4500 (estimate)
Flash point:
>230 °F
storage temp. 
2-8°C
solubility 
The solubility of o-phthalaldehyde is 3g/100 mL diisopropyl ether, 5g/100mL deionized water, 20g/100mL chloroform, or 20g/100mL acetone at 20°C.
form 
powder
color 
yellow
PH
7 (53g/l, H2O, 20℃)
Water Solubility 
soluble
Sensitive 
Air Sensitive
Merck 
14,7368
BRN 
878317
Exposure limits
ACGIH: SL .025 mg/100 cm2; Ceiling 0.1 ppb (Skin)
Stability:
Stable. Air sensitive. Incompatible with strong oxidizing agents, strong bases.
InChIKey
ZWLUXSQADUDCSB-UHFFFAOYSA-N
LogP
0.99 at 30℃
CAS DataBase Reference
643-79-8(CAS DataBase Reference)
NIST Chemistry Reference
O-phthalaldehyde(643-79-8)
EPA Substance Registry System
1,2-Benzenedicarboxaldehyde (643-79-8)
More
Less

Safety

Hazard Codes 
Xi,T,N,C
Risk Statements 
36/37/38-43-34-25-50-52/53
Safety Statements 
26-28-36-45-36/37/39-61-37/39
RIDADR 
UN2923 8/PG 2
WGK Germany 
3
RTECS 
TH6950000
1-8-10
Autoignition Temperature
480 °C
Hazard Note 
Irritant/Air Sensitive
TSCA 
Yes
HazardClass 
8
PackingGroup 
HS Code 
29122900
Hazardous Substances Data
643-79-8(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: 178 mg/kg LD50 dermal Rat > 2000 mg/kg
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H301Toxic if swalloed

H314Causes severe skin burns and eye damage

H317May cause an allergic skin reaction

H335May cause respiratory irritation

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
8.21027
Product name
Phthaldialdehyde
Purity
for synthesis
Packaging
500mg
Price
$49.2
Updated
2024/03/01
Sigma-Aldrich
Product number
8.21027
Product name
Phthaldialdehyde
Purity
for synthesis
Packaging
10g
Price
$130
Updated
2024/03/01
Sigma-Aldrich
Product number
8.21027
Product name
Phthaldialdehyde
Purity
for synthesis
Packaging
50g
Price
$375
Updated
2024/03/01
Sigma-Aldrich
Product number
79760
Product name
Phthaldialdehyde
Purity
for fluorescence, ≥99.0% (HPLC)
Packaging
1g
Price
$228
Updated
2024/03/01
Sigma-Aldrich
Product number
79760
Product name
Phthaldialdehyde
Purity
for fluorescence, ≥99.0% (HPLC)
Packaging
5g
Price
$708
Updated
2024/03/01
More
Less

o-Phthalaldehyde Chemical Properties,Usage,Production

Chemical Properties

o-Phthalaldehyde is a pale yellow crystalline solid.

o-Phthalaldehyde is mainly used as a high-level disinfectant (a low-temperature chemical method) for heat-sensitive medical and dental equipment such as endoscopes and thermometers; in recent years, it has gained popularity as a safe and better alternative to glutaraldehyde.
There are some researches show, pH7.5 contains the sterilizing agent of o-phthalaldehyde 0.5%, and its sterilizing power, sterilization speed, stability and toxicity all are better than glutaraldehyde, can kill mycobacterium in the 5min, the bacterium number reduces by 5 logarithmic value, and o-phthalaldehyde is very stable, tasteless in pH3~9 scopes, non-stimulated to human nose, eye mucosa, and need not activate before using, various materials are had good consistency, have tangible microbiocidal activity.

Uses

o-Phthalaldehyde can be widely used for precolumn derivatization of amino acids in HPLC separation or Capillary electrophoresis. For flow cytometric measurements of protein thiol groups.

Uses

Disinfectant. Reagent in fluorometric determination of primary amines and thiols.

Uses

Precolumn derivatization reagent for primary amines and amino acids. The fluorescent derivative can be detected by reverse-phase HPLC. The reaction requires OPA, primary amine and a sulfhydryl. In the presence of excess sulfhydryl, amines can be quantitated. In the presence of excess amine, sulfhydryls can be quantitated.

Definition

ChEBI: A dialdehyde in which two formyl groups are attached to adjacent carbon centres on a benzene ring.

Preparation

o-Phthalaldehyde is a high-level chemical disinfectant that is commonly used for disinfection of dental and medical instruments as an alternative to glutaraldehyde, which is a known skin and respiratory sensitizer.
A variety of processes for manufacturing o-phthalaldehyde have been reported in the literature.
o-Phthalaldehyde is produced by heating pure benzaldehyde and chloroform with potassium hydroxide solution. The resulting solution is further acidified with hydrochloric acid and cooled to yield a colorless powder of o-phthalaldehyde.
It is also produced by ozonization of naphthalene in alcohol followed by catalytic hydrogenation.
Catalytic oxidation of various chemicals is also used in manufacturing o-phthalaldehyde. o-Phthalaldehyde can be manufactured by oxidation of phthalan by nitrogen monoxide in acetonitrile with N-hydroxyphthalimide as the catalyst to yield 80% to 90%.

Definition

Using o-phthalaldehyde (OPA) in combination with a thiol reagent is a standard method for detecting primary amines in amino acids, peptides, and proteins. O-phthalaldehyde, in the presence of 2-mercaptoethanol, reacts with primary amines to form highly fluorescent products. Picomole quantities of amino acids, peptides, and proteins can be detected easily. o-Phthalaldehyde is five to ten times more sensitive than fluorescamine and is soluble and stable in aqueous buffers. Despite its widespread use, the exact reaction mechanism has been debated since the 1980s. Rovelli's results support the mechanism originally proposed by Sternson and Wong, in which the primary amine first reacts with OPA, followed by a reaction with the thiol to form the fluorescent isoindole product[1-2].

Synthesis Reference(s)

Journal of the American Chemical Society, 73, p. 1668, 1951 DOI: 10.1021/ja01148a076
Tetrahedron Letters, 27, p. 1793, 1986 DOI: 10.1016/S0040-4039(00)84377-4

Reactivity Profile

o-Phthalaldehyde (OPA)-amine reaction and OPA-amine-thiol reaction have been developed to effectively modify native peptides and proteins under the physiological conditions. First, OPA and its derivatives can rapidly and smoothly react with primary amine moieties in peptides and proteins to achieve native protein biconjugations. Furthermore, OPA-alkyne bifunctional linkers can be used for proteome profiling. Second, OPA-amine-thiol three-component reaction has been developed for chemoselective peptide cyclization, directly on unprotected peptides in the aqueous buffer. Moreover, this OPA-guided cyclic peptide can be further modified with the N-maleimide moiety in one pot to introduce additional functionalities[3].

Flammability and Explosibility

Not classified

Biological Activity

Phthaldialdehyde can be used for the pre-column derivatization of amino acids for high-performance liquid chromatography (HPLC) separation. It may also be used for flow cytometric measurements of protein thiol groups.

Biotechnological Applications

O-phthalaldehyde(OPA) is used for precolumn derivatization of amino acids for HPLC separation and for flow cytometric measurements of protein thiol groups. Used for fluorometric determination of histamine, histidine and other amino acids. Also used for cholesterol assay in the picomole range.
Phthaldialdehyde has been used:
in the preparation of O-phthaldialdehyde reagent for analysing gentamycin content.
in the preparation of reagent for determining the degree of hydrolysis of milk proteins.
in the measurement of free amino acids of milk samples by O-phthaldialdehyde/N-acetyl-L-cysteine (OPA/NAC) assay.
in the derivatization of putrescine samples.

Potential Exposure

The primary routes of human exposure to o-phthalaldehyde are by inhalation and through the skin, which may occur through accidental or occupational exposures. Along with its increasing popularity as a chemical sterilizer, o-phthalaldehyde has many applications in analytical methods and in diagnostic kits. o-Phthalaldehyde is also used as an intermediate in the synthesis of pharmaceuticals and as a reagent in the tanning industry, hair colorings, wood treatment, and antifouling paints. o-Phthalaldehyde was approved for use as an indoor antimicrobial pesticide in 1997; however, it is no longer registered with the United States Environmental Protection Agency (USEPA) for this use.

Carcinogenicity

No information on the carcinogenicity of o-phthalaldehyde in experimental animals or humans was found in a review of the literature.

References

[1] Grazia Rovelli, Kevin R Wilson. “Elucidating the Mechanism for the Reaction of o-Phthalaldehyde with Primary Amines in the Presence of Thiols.” The Journal of Physical Chemistry B 127 14 (2023): 3257–3265.
[2] J R Benson, ;P E Hare. “O-phthalaldehyde: fluorogenic detection of primary amines in the picomole range. Comparison with fluorescamine and ninhydrin.” Proceedings of the National Academy of Sciences of the United States of America 72 2 (1975): 619–22.
[3] “Chemical Tools for Imaging, Manipulating, and Tracking Biological Systems: Diverse Methods for Optical Imaging and Conjugation.” Methods in enzymology 1 1 (1900).

o-Phthalaldehyde Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

o-Phthalaldehyde Suppliers

Jinan Finer Chemical Co., Ltd
Tel
15662658101
Fax
0531-88989539
Email
sales@finerchem.com
Country
China
ProdList
315
Advantage
58
Beijing Century Richap Chemistry Co., Ltd.
Tel
010-64446226
Fax
+86 10 64455595
Email
info@bj-newcenturychem.com
Country
China
ProdList
111
Advantage
55
Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
400-6206333 1316706386
Fax
021-50323701
Email
anhua.mao@aladdin-e.com
Country
China
ProdList
25003
Advantage
65
Shandong Zouping Xinlong Technology Co., Ltd.
Tel
0543-4260076 13696309696
Fax
0543-4260076
Email
5042407@qq.com
Country
China
ProdList
58
Advantage
58
Hubei deante Chemical Technology Co., Ltd
Tel
15927262683
Email
3244356795@qq.com
Country
China
ProdList
849
Advantage
58
Hubei Baoling Chemical Technology Co. , Ltd.
Tel
13129969326
Email
2797487194@qq.com
Country
China
ProdList
1008
Advantage
58
Hubei Chenghai Chemical Co., Ltd
Tel
18327245847 18327245847
Email
1400838877@qq.com
Country
China
ProdList
9957
Advantage
58
ZEUS CHEM LTD
Tel
180-71545453 18071542427
Fax
1735832116
Email
tina@zeuschem.cn
Country
China
ProdList
332
Advantage
58
Hubei YiKangYuan Chemical Co., Ltd.
Tel
027-87182908 18064088908
Fax
027-87182900
Email
65824125@qq.com
Country
China
ProdList
92
Advantage
55
Shanghai Boyle Chemical Co., Ltd.
Tel
021-50182298 021-50180596
Fax
+86-21-57758967
Email
sales@boylechem.com
Country
China
ProdList
2208
Advantage
55
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30123
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Beijing dtftchem Technology Co., Ltd.
Tel
010-60275820 13031183356
Fax
010-60270825
Email
elainezt@sina.com
Country
China
ProdList
1390
Advantage
62
Beijing HwrkChemical Technology Co., Ltd
Tel
010-89508211 18501085097
Fax
010-89508210
Email
sales.bj@hwrkchemical.com
Country
China
ProdList
9371
Advantage
55
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44733
Advantage
61
Capot Chemical Co., Ltd
Tel
+86 (0) 571 85 58 67 18
Fax
0086-571-85864795
Email
sales@capotchem.com
Country
China
ProdList
18207
Advantage
66
Beijing Ouhe Technology Co., Ltd
Tel
010-82967028 13552068683
Fax
+86-10-82967029
Email
2355560935@qq.com
Country
China
ProdList
12443
Advantage
60
JinYan Chemicals(ShangHai) Co.,Ltd.
Tel
13817811078
Fax
86-021-50426522,50426273
Email
sales@jingyan-chemical.com
Country
China
ProdList
9976
Advantage
60
Accela ChemBio Co.,Ltd.
Tel
021-50795510 4000665055
Fax
021-50795055
Email
sales@accelachem.com
Country
China
ProdList
11655
Advantage
64
Shanghai Longsheng chemical Co.,Ltd.
Tel
021-58099652-8005 13585536065
Fax
021-58099609
Email
bin.wu@shlschem.com
Country
China
ProdList
9810
Advantage
59
Shanghai Harvest Chemical Industrial Co., Ltd.
Tel
21-31038972 15721252604
Fax
+86-21-51385350
Email
ammyzuo@harvest-chem.com
Country
China
ProdList
2541
Advantage
64
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Country
China
ProdList
42958
Advantage
64
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
32321
Advantage
50
XiaoGan ShenYuan ChemPharm co,ltd
Tel
15527768850
Email
1791901229@qq.com
Country
China
ProdList
8834
Advantage
52
Shandong Xiya Chemical Co., Ltd
Tel
4009903999 13355009207
Fax
0539-6365991
Email
3007715519@qq.com
Country
China
ProdList
18736
Advantage
57
shanghai Rainbow MediTech.Co.Ltd.
Tel
21-021-64968085,64968086-5815,5812 13918693646
Fax
+86 21 64968087
Email
bd@rainbowpharma.cn
Country
China
ProdList
978
Advantage
65
Sichuan Kulinan Technology Co., Ltd
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11707
Advantage
57
Tianjin heowns Biochemical Technology Co., Ltd.
Tel
400 638 7771
Email
sales@heowns.com
Country
China
ProdList
14435
Advantage
57
Sinopharm Chemical Reagent Co,Ltd.
Tel
86-21-63210123
Fax
86-21-63290778 86-21-63218885
Email
sj_scrc@sinopharm.com
Country
China
ProdList
9815
Advantage
79
Wuhan Kemi-Works Chemical Co., Ltd
Tel
027-85736489
Fax
86-27-85736485
Email
info@kemiworks.net
Country
China
ProdList
540
Advantage
57
Shanghai Sunway Pharmaceutical Technology Co., Ltd
Tel
021-51613915-820 13611835272
Fax
021 51613951
Email
mmwang@sunwaypharm.cn
Country
China
ProdList
9734
Advantage
57
Maya High Purity Chemicals
Tel
+86 (573) 82222445 (0)18006601000 452520369
Fax
+86 (573) 82222643
Email
sales@maya-r.com
Country
China
ProdList
11707
Advantage
57
Springchem New Material Technology Co.,Limited
Tel
+86-021-62885108 +8613917661608
Email
info@spring-chem.com
Country
China
ProdList
2068
Advantage
57
ZhengZhou HuaWen Chemical Co.Ltd
Tel
0370-2785118 17550508557
Fax
QQ:3470079902
Email
675141927@qq.com
Country
China
ProdList
3203
Advantage
55
Spectrum Chemical Manufacturing Corp.
Tel
021-021-021-67601398-809-809-809 15221380277
Fax
021-57711696
Email
marketing_china@spectrumchemical.com
Country
China
ProdList
9658
Advantage
60
TaiZhou ZhiCheng Chemicals & Technology Co., LTD.
Tel
0523-82837785 13914525028
Fax
0523-87913272
Email
info@jszchg.com
Country
China
ProdList
250
Advantage
60
Dalian Meilun Biotech Co., Ltd.
Tel
0411-62910999 13889544652
Email
sales@meilune.com
Country
China
ProdList
4727
Advantage
58
ShangHai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847 13636370518
Fax
021-55068248
Email
shyysw007@163.com
Country
China
ProdList
4940
Advantage
60
Chengdu Ai Keda Chemical Technology Co., Ltd.
Tel
4008-755-333 18080918076
Fax
028-86757656
Email
800078821@qq.com
Country
China
ProdList
9718
Advantage
55
AILY INTL CHEMICAL CORP LTD
Tel
025-83208295 18913388297
Fax
+86-2583208202
Email
ben@ailychem.com
Country
China
ProdList
132
Advantage
50
Shanghai civi chemical technology co.,Ltd
Tel
86-21-34053660
Fax
86-21-34053661
Email
sale@labgogo.com
Country
China
ProdList
9865
Advantage
52
Thermo Fisher Scientific
Tel
800-810-5118
Fax
+86-10-84193589
Email
cnchemical@thermofisher.com
Country
China
ProdList
17770
Advantage
75
Beijing innoChem Science & Technology Co.,Ltd.
Tel
400-810-7969 010-59572699
Fax
010-59572688
Email
ningzi.li@inno-chem.com.cn
Country
China
ProdList
6134
Advantage
55
Shanghai T&W Pharmaceutical Co., Ltd.
Tel
+86 21 61551611
Fax
+86 21 50676805
Country
China
ProdList
9891
Advantage
58
9ding chemical ( Shanghai) Limited
Tel
4009209199
Fax
86-021-52271987
Email
sales@9dingchem.com
Country
China
ProdList
18209
Advantage
56
Shanghai Zhuorui Chemical Co.,Ltd.
Tel
021-69180038
Fax
0086-21-39177059
Email
zhuoruichem@163.com
Country
China
ProdList
105
Advantage
58
Cantotech Chemicals, Ltd.
Tel
86-0755-86635001
Fax
86-0755-22642228
Email
cantotech@126.com
Country
China
ProdList
4566
Advantage
55
Shanghai Yolne Chemical Co., Ltd.
Tel
021-62960152
Fax
021-52212593
Email
934678158@qq.com
Country
China
ProdList
9899
Advantage
55
More
Less

View Lastest Price from o-Phthalaldehyde manufacturers

Jinan Finer Chemical Co., Ltd
Product
o-Phthalaldehyde 643-79-8
Price
US $0.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
200mt
Release date
2022-04-19
Hebei Dangtong Import and export Co LTD
Product
o-Phthalaldehyde 643-79-8
Price
US $75.00-60.00/kg
Min. Order
1000kg
Purity
99%
Supply Ability
50 Tons
Release date
2024-09-13
Hebei Zhuanglai Chemical Trading Co.,Ltd
Product
o-Phthalaldehyde 643-79-8
Price
US $85.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
5000kg/week
Release date
2024-04-26

643-79-8, o-PhthalaldehydeRelated Search:


  • The developMent of forMaldehyde
  • O-PHTHALDIALDEHYDE REAGENT SOLUTION*
  • PHTHALALDEHYDE
  • TIMTEC-BB SBB008450
  • 2-PHTHALALDEHYDE
  • 2-PHTHALDEHYDE
  • 2-PHTHALDIALDEHYDE
  • o-Phenyldialdehyde
  • 1,2-Phthalic dicarboxaldehyde, 98+%
  • O-PHTHALALDEHYDE,REAGENT
  • O-PHTALDIALDEHYDE
  • BENZENE-1,2-DICARBOXALDEHYDE
  • BENZENE-1,2-DIALDEHYDE
  • FLUORALDEHYDE(TM) O-PHTHALALDEHYDE
  • O-PHTALALDEHYDE
  • o-Phthalaldehyde (1.11452)
  • o-Phthaldialdehyde OPD
  • P-phthaladyhyde
  • O-PHTHALDIALDEHYDE REAGENT SOLUTION*INCO MPLETE
  • PHTHALDIALDEHYDE, FOR FLUORESCENCE
  • O-PHTHALDIALDEHYDE REAGENT SOLUTION*COMP LETE
  • O-PhthalaldehydeA.R.
  • O-PhthalaldehydeGr(ForFluorometry)
  • 2-Phthalaldehdye
  • o-PHTHALALDEHYDE GR
  • Phthalaldehyde=Phthaldialdehyde
  • 1,2-BENZENEDICARBALDEHYDE
  • 1,2-BENZENEDICARBOXALDEHYDE
  • 1,2-PHTHALIC DICARBOXALDEHYDE
  • o-Phthaldialdehyde,98%
  • Ortho-Phthalaldehyde (1,2 – benzenedicarboxaldehyde
  • Phthaldialdehy
  • o-PhthaL
  • o-Phthaladehyde
  • phtalaldehydes
  • Phthalaldialdehyde
  • Phthalic aldehyde
  • Phthalic dialdehyde
  • Phthalyldicarboxaldehyde
  • CIDEX-OPA
  • ORTHO-PHTHALALDEHYDE
  • O-PHTHALIC DICARBOXALDEHYDE / PHTHALDIALDEHYDE
  • O-PHTHALIC DIALDEHYDE
  • O-PHTHALIC DICARBOXALDEHYDE
  • o-phthalic aldehyde
  • O-PHTHALALDEHYDE
  • O-PHTHALALDIALDEHYDE
  • O-PHTHALDEHYDE
  • O-PHTHALDIALDEHYDE
  • OPA
  • OPD
  • ORTHO-PHTHALADEHYDE
  • PHTHALIC DICARBOXALDEHYDE
  • PHTHALDIALDEHYDE
  • PHTHALDIALDEHYDE REAGENT
  • o-benzenedicarbonal
  • phthaldehyde
  • Benzene-1,2-dicarboxaldehyde, OPA